APPLICATION OF HERBAL PLANTS USED IN THE TREATMENT FOR HYPERTENSION DISEASE

Global Journal of Pharmaceutical and Scientific Research (GJPSR)

APPLICATION OF HERBAL PLANTS USED IN THE TREATMENT FOR HYPERTENSION DISEASE

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Volume-1, Issue-2, September- 2025

Article Received on 29/07/2025                                Article Revised on 12/08/2025                              Article Accepted on 01/09/2025 

APPLICATION OF HERBAL PLANTS USED IN THE TREATMENT FOR HYPERTENSION DISEASE 

1Pushpendra Kumar, 2Vishnu Prasad Yadav, 2Prabha Manjari Shukla, 2Ajay Kumar Shukla, 3Aarti Tiwari,

1Faculty of Pharmacy, Uttar Pradesh University of Medical Sciences Saifai Etawah UP

2Institute of Pharmacy, Dr Rammanohar Lohia Avadh University Ayodhya UP

3Department of Pharmacy, Guru Ghasidas Vishwavidyalaya is a central University in Bilaspur, Chhattisgarh, India

Corresponding Author: Pushpendra Kumar

 

Abstract

Hypertension, commonly referred to as high blood pressure, is one of the leading risk factors for cardiovascular morbidity and mortality worldwide. Although several classes of synthetic antihypertensive agents are available, their long-term use is often associated with side effects, poor patient compliance, and economic burden. In recent years, herbal plants have gained significant attention as complementary and alternative therapies for the management of hypertension due to their affordability, safety profile, and rich phytoconstituents with diverse pharmacological actions. Various medicinal plants such as Allium sativum, Moringa oleifera, Ocimum basilicum, Phyllanthus amarus, Punica granatum, Raphanus sativus, Rauwolfia serpentine, Sesamum indicum and Zingiber officinale have demonstrated antihypertensive effects through mechanisms including vasodilation, diuresis, calcium channel blockade, ACE inhibition, antioxidant activity, and modulation of lipid metabolism. Scientific investigations, encompassing phytochemical screening, in vitro and in vivo studies, and clinical trials, have validated their potential role in lowering blood pressure and improving cardiovascular health. However, challenges remain in terms of standardization, dosage optimization, safety evaluation, and herb–drug interactions. This review highlights the therapeutic potential of herbal plants in hypertension management and emphasizes the need for further research to develop standardized, evidence-based phytopharmaceuticals for effective and safe clinical use.

Keywords: Hypertension, synthetic antihypertensive agents, herbal plants, calcium channel blockade, ACE inhibition, antioxidant activity, and modulation of lipid metabolism, phytochemical screening.

1. Introduction

Hypertension is defined as an abnormally high blood pressure (BP) and is one of the most important risk factors for cardiovascular disease and death. The limits that define hypertension are chosen to reflect the risk for disease related to the elevated BP although risk increases even within the ‘normal’ BP range. Hypertension is a risk factor for stroke, myocardial infarction (MI), left ventricular hypertrophy (LVH) and failure, renal disease, retinopathy, and peripheral arterial disease. Therefore, effective evaluation and treatment of hypertension remains an important medical goal, and understanding the pathogenesis of hypertension through animal models and clinical studies is a critical component.

Hypertension can be due to unknown causes, primary hypertension (previously called essential hypertension), or known causes, secondary hypertension. Primary hypertension accounts for about 85–90% of the cases of hypertension, which is lower than often quoted in most textbooks. The lower percentage is due to the recent appreciation of the role of primary aldosterone, which was once thought to be rare (< 1%) but is now known to constitute between 10% and 15% of hypertensive cases. Primary hypertension clusters in families and shows concordance in genetically related individuals illustrating the importance of genetic predisposition. The known inheritable syndromes regulating BP are caused by mutations regulating renal sodium handling.

Hypertension is also commonly called high Blood Pressure i.e. above 140/90 and it is severe above 180/120. Hypertension symptoms are not known as such but a person should be carefully observed for the underlying problems or signs as it are a serious, long-term or chronic health problem that may occur due to other illnesses. Therefore, it is important to keep track of the warning signs of Hypertension as prevention is better than cure. It is a primary risk factor for various cardiovascular diseases including Stroke, Heart Failure, Heart Attack and Aneurysm. It is thus important to keep Blood Pressure under control and preserve a healthy body by preventing occurrence of other lifestyle diseases too. It is related to the Pressure or the force exerted by the Blood against the Blood vessels’ walls. It is very common to occur in today’s lifestyle and affects over one billion people worldwide.The two kinds of Hypertension are known, namely [1].

Primary Hypertension: It is also known as essential Hypertension and it is the high Blood Pressure that doesn't occur through a known secondary cause. 

Secondary Hypertension: It is the high Blood Pressure caused due to another medical condition and it can affect our kidneys, heart, arteries or endocrine system. Some of the medications or illegal drugs can also cause secondary Hypertension

Genetic factors interact with environmental factors to produce hypertension. Diet is an important determinant both in its salt content and in the increasing public health problem of obesity. Dietary salt may have chronic effects and relate to the observed increases in BP in Western societies with age. Obesity is now known to be a chronic inflammatory disease that increases the risk of hypertension and likely relates to the interaction of hypertension in increasing the risk of cardiovascular disease [2].

Abnormalities in a number of systems are seen in primary hypertension, yet the originating causes have remained elusive. Neural systems show an increased sympathetic flow with elevations of catecholamines. Central nervous system (CNS) interventions in a number of experimental systems can alter BP and prevent hypertension. The sympathetic system interacts with the hormonal systems that involve adrenal catecholamines and the important action of the renin–angiotensin–aldosterone system (RAAS). The RAAS involves multiple organs with the primary role of the kidney and adrenal cortex (glomerulosa layer producing aldosterone). It is the major hormonal regulator of sodium and volume homeostasis and hence a major regulator of BP. Many of the pharmacological interventions used clinically to treat hypertension target this system. Defects in the vascular endothelial and smooth muscle cell function have been described

Many people have high blood pressure (hypertension). But they usually don't notice it which means that over time it can damage blood vessels. Having blood pressure that is always too high can make you more likely to have a heart attack, a stroke or kidney problems. The higher your blood pressure is the greater your risk of developing these medical conditions [2, 3].

Blood pressure readings have two values that are always listed together: 128/85 mmHg, for example. The first number represents the pressure in the blood vessels when the heart muscles squeeze (systolic blood pressure). The second represents the pressure in the blood vessels when the heart muscles relax (diastolic blood pressure) [2, 3].

Blood pressure is considered to be too high if the systolic value is over 140 and/or the diastolic value is over 90. But these levels were set for practical reasons and act only as a general guide. Because of this, recommendations about when medication is needed to treat high blood pressure may vary [2, 3].

2. Symptoms of Hypertension

Generally, there are no symptoms or signs specific to Hypertension. However, one can observe headaches, shortness of breath, bleeding of nose and uneasiness in people starting with Hypertension. Until Hypertension reaches its severity, symptoms do not occur intensely.

It is best to prevent Hypertension and related problems by keeping an eye on your Blood Pressure. If you are 40 or older, it is necessary to track your Blood Pressure readings twice or thrice a month or more if you feel uneasiness about your health. Even young people are vulnerable towards it because of today’s lifestyle and lack of exercise, so they are also advised to have knowledge about Hypertension, keep track of their BP and take all measures to keep oneself healthy. Besides manual BP machines, Digital BP machines are also easily available in the market, people can even buy and keep it at home for convenient tracking. Please do not neglect the following symptoms that can be due to development of Hypertension in a person

• Dizziness

• Bleeding Nose

• Chest Pain

• Heart attack

• Headaches    

• Visual Changes

• Shortness of Breath

• Flushing or Blushing

• Narrowing of Blood vessels

• Formation of plagues in the Blood vessels [4].

3. Causes of Hypertension

Causes for Hypertension include various factors including Obesity, Hereditary (family history) and other lifestyle factors. It is manageable through proactive and consistent steps such as inculcating the habit of regular physical exercise, meditation and various stress reducing techniques, medications, preventing excess salt and junk food, etc

• Dizziness

• Bleeding Nose

• Chest Pain

• Heart attack

• Headaches    

• Visual Changes

• Shortness of Breath

• Flushing or Blushing

• Narrowing of Blood vessels

• Formation of plagues in the Blood vessels

4. Various Factors Contributing to Cause Hypertension Include:

• Diabetes

• Pregnancy

• Cushing syndrome

• Hyperthyroidism

• Kidney problems

• Obesity

• Adrenal hyperplasia [5].

5. Risk factors

Our bodies are able to regulate blood pressure as needed. It's typically low when we relax or sleep. It increases when, for example, we do hard physical work and our muscles need more blood. Stress or fear can also cause your blood pressure to go up. It usually naturally increases with age in most people as well.

So it's normal for blood pressure readings to vary; that's just a sign of an active life. But if blood pressure is too high for too long, it can damage blood vessels over time and increase the risk of various health problems.

Often no specific cause is found for high blood pressure. Then doctors call it "essential" or "primary" hypertension.

Being overweight, eating a lot of salt, drinking too much alcohol and not getting enough exercise can increase your blood pressure. But slim, athletic people who watch what they eat may also develop high blood pressure – for example, because it runs in their family.

An exact cause is only found in 5 out of 100 people. Possible causes include an overactive thyroid gland (hyperthyroidism) or kidney disease. When the cause is known, doctors refer to it as "secondary" hypertension.

Sometimes medications can increase blood pressure as well. For example:

• Some medicines used to treat psychological illnesses

• Certain plant-based medications like St. John's wort

• Decongestant nasal sprays or drops

• Birth control pills [6].

6. Effects

Long-term high blood pressure can increase the likelihood of cardiovascular (heart and blood vessel) diseases and cause organ damage. The possible long-term effects of high blood pressure include the following:

• Poor blood circulation in the legs (PAD)

• Weak heart (myocardial insufficiency, heart failure)

• Heart attack

• Stroke

• Damage to the kidneys

Treatment can lower the risk of developing these kinds of problems.

7. Diagnosis

Blood pressure is measured in units of “millimeters of mercury,” written “mmHg” for short. It is always measured while you are resting so that the readings can be compared and interpreted more easily. Blood pressure is measured on several days to get a more reliable result than a single reading can offer. It's also important to measure blood pressure on both arms because the pressures may differ. The highest systolic reading and the highest diastolic reading are then taken as the basis for determining your blood pressure.

An adult’s blood pressure is considered to be normal if it is less than 140 over 90 (140/90). High blood pressure is diagnosed if

• The systolic reading is greater than 140 mmHg,

• The diastolic reading is greater than 90 mmHg, or

• Both readings are greater than these values.

Sometimes blood pressure is measured over a 24-hour period (ambulatory blood pressure monitoring). This might be done if individual measurements vary a lot. To do that, you carry a portable instrument with you that measure your blood pressure at regular intervals [7].

8. Screening

In Germany, statutory health insurers cover the cost of a general health check-up every three years from the age of 35 onwards. The aim of this check-up is to detect early signs of cardiovascular disease, diabetes and kidney problems. It includes taking your blood pressure. So far, though, studies haven’t proven that regular general health check-ups can protect healthy people from illness or increase their life expectancy.

9. Prevention of Hypertension

In today’s era, it is important to keep oneself healthy and prevent chronic conditions such as Hypertension. By taking certain steps, one can prevent Hypertension from occurring and even manage it if it already exists. Following are some of the must do activities in day to day life:

• Reducing salt intake in diet

• No consumption of alcohol

• Consumption of plenty of fruits and vegetables

• Avoiding calorie-rich or junk food

• Walking for 30-40 minutes daily 

• Alternative regular physical exercise program 

• Meditation or other stress buster activities

• High Blood Pressure is another name for high Blood Pressure. It causes serious health complications and can increase the risk of heart disease, stroke, and sometimes death. 

• Blood Pressure is the force that human Blood exerts on the walls of Blood vessels. This Pressure is working on the basis of the resistance of the Blood vessels and how hard the heart must work. 

• Almost half of adults in the United States have high Blood Pressure, but many may not be aware of it.

• Hypertension is an important risk factor for cardiovascular diseases such as stroke, heart attack, heart failure and aneurysms. Controlling Blood Pressure is important for maintaining good health and reducing the risk of these dangerous conditions. 

• Read below to find out why your Blood Pressure is rising, how to monitor your Blood Pressure, and how to keep your Blood Pressure within normal limits.

10. Management and Treatment 

• Keeping a track of lifestyle is the standard first-line treatment for Hypertension. Here are some recommendations: 

• Regular Exercise 

• Current guidelines recommend that everyone, including those with high Blood Pressure, do at least 150 minutes of medium-intensity aerobic exercise or 75 minutes of high-intensity exercise each week. .. 

• In addition to 150 minutes of exercise, most adults benefit from strength training at least twice a week. 

• People need to exercise at least 5 days a week [8].

Examples of Suitable Activities are: 

1. Walking 

2. Jogging 

3. Biking 

4. Swimming

11. Relieving Stress 

Learning to Avoid and Manage Stress Helps People Control Blood Pressure. 

Here are some relaxation techniques that can help reduce stress. 

1. Meditation 

2. Hot bath 

3. Yoga 

4. Long walk

• Avoid alcohol and recreational drugs to manage stress. These can contribute to high Blood Pressure and complications of high Blood Pressure. 

• Smoking can also increase Blood Pressure. Avoiding or quitting smoking reduces the risk of high Blood Pressure, serious heart disease, and other health problems.

12. Medications 

• People may take certain medications to treat high Blood Pressure. Doctors often recommend low doses first. Antihypertensive drugs usually have few side effects. 

• People with high Blood Pressure may need to combine two or more medications to control their Blood Pressure [6-9].

13. Antihypertensive Drugs Include: 

Diuretics:

Loop diuretics: Bumetanide, Ethacrynic acid, Furosemide, Torsemide

Thiazide diuretics:, Epitizide, Hydrochlorothiazide, Chlorothiazide, Bendroflumethiazide

Thiazide-like diuretics: Indapamide, Chlorthalidone, Metolazone

Potassium-sparing diuretics: Amiloride, Triamterene, Spironolactone

Adrenergic receptor antagonists:

Beta blockers: Atenolol, Metoprolol, Nadolol, Oxprenolol, Pindolol, Propranolol, Timolo

Alpha blockers: Doxazosin, Phentolamine, Indoramin, Phenoxybenzamine, Prazosin, Terazosin, Tolazoline

Mixed Alpha + Beta blockers: Bucindolol, Carvedilol, Labetalol

Adrenergic receptor agonists:

Alpha-2 agonists: Clonidine, Methyldopa, Guanfacine

Calcium channel blockers:

Dihydropyridines: Amlodipine, Felodipine, Isradipine, Lercanidipine, Nicardipine, Nifedipine, Nimodipine, Nitrendipine

Non-dihydropyridines: Diltiazem, Verapamil

ACE inhibitors: Captopril, Enalapril, Fosinopril, Lisinopril, Perindopril, Quinapril, Ramipril, Trandolapril, Benazepril

Angiotensin II receptor antagonists: Valsartan, Candesartan, Eprosartan, Irbesartan, Losartan, Olmesartan, Telmisartan.

Aldosterone antagonists: Eplerenone, Spironolactone.

Vasodilators: Sodium nitroprusside, Hydralazine.

Centrally acting adrenergic drugs: Clonidine, Guanabenz, Methyldopa, Moxonidine [10].

14. Diet 

People can prevent high Blood Pressure by eating good heart nutrition. 

• Reduced salt intake 

• High sodium consumption can lead to high Blood Pressure. The major source of sodium in food is salt. 

• The American Heart Association recommends that people without high Blood Pressure consume less than 2,300 milligrams (mg) of sodium per day. This is about the right amount of a teaspoon. People with high Blood Pressure need less than 1,500 mg of sodium per day to control their condition. 

• Reducing salt intake can benefit people with or without high Blood Pressure. 

• Facilitating drinking 

• Moderate to high doses can increase Blood Pressure.

Experts recommend that people with high Blood Pressure prefer foods that are good for heart health, such as

1. Various fruits and vegetables 

2. Legumes such as chickpeas, legumes and lentils 

3. Nuts 

4. Omega 3 rich fish 

4 Twice a week 

5. Non-tropical plant oils such as olive oil 

6. Skinless poultry and fish 

7. Low-fat dairy products 

• Avoid Trans fats, hydrogenated vegetable oils, animal fats, and processed fast foods when planning your diet if a person has high Blood Pressure or wants to maintain moderate Blood Pressure. 

• Omega 3 fatty acids in oily fish and olive oil have a protective effect on the heart. But these are still bold. They are usually healthy, but people with high Blood Pressure still need to include them in their total fat intake.  Weight Management 

• Overweight can contribute to high Blood Pressure. A decrease in Blood Pressure usually follows a loss of weight. This is because the heart does not have to work hard to pump Blood around the body. 

• It helps to have a balanced diet with calorie intake appropriate for your height, gender, and activity level [11].

Dietary modification 

DASH-trial proved reductions in BP of 11.4/5.5 mmHg in persons having hypertension on a diet rich in fruits, vegetables, and low-fat dairy products, compared with those people who were on a so-called “usual American diet”. Dietary salt intake and weight were kept constant. Another two clinical trials, one with a comprehensive food plan that supplied the recommended dietary allowances of all major nutrients and the other with a diet rich in fruits, vegetables, and low-fat dairy products and reduction in saturated and total fat produced reductions in BP comparable to or greater than those usually seen with monotherapy for stage 1 hypertension. Dietary salt intakes have a linear association with blood pressure. Reduced sodium intake to approximately 100 mmol day-1 can prevent the development of hypertension [12].

Weight loss and physical activity 

Overweight (body mass index >25 kg/m2) has been seen in epidemiologic studies to be an important risk factor for higher blood pressure, and there seems to be a linear relation between body weight and blood pressure. Clinical trials have shown that weight loss, specially when combined with dietary sodium restriction, lowers blood pressure in hypertensive and also in normotensive patients. The Hypertension Prevention Trial showed that a 4 % reduction in body weight over 3 years was associated with a 2.4 mmHg reduction in SBP and a 1.8 mmHg reduction in DBP. 63 Increasing aerobic physical activity such as brisk walking, jogging, swimming or bicycling has been shown to lower BP. A meta-analysis of 54 randomized controlled trials showed a net reduction of 3.8 mmHg in SBP and 2.6 mmHg in DBP in individuals performing aerobic exercises, compared to controls [13].

13. Pharmacological treatment 

As blood pressure increases, it become more difficult to control it at the target level through life style modifications alone and treatment with antihypertensive drugs becomes necessary. WHO guidelines also recommend the use of antihypertensive drugs in patients with grade 1 hypertension at low or moderate cardiovascular risk, that is, when BP is between 140 and 159 mmHg SBP and/or 90 and 99 mmHg DBP, provided non pharmacological treatment has proved unsuccessful. So, in these conditions the patient should move towards pharmacological treatment

Diuretics

The steady introduction of newer agents and their heavy promotion by the industry made physicians switch away from use of diuretics as first line agents in the treatment of mild to moderate hypertension but then also thiazide type of diuretics offer better reduction of blood pressure with lesser incidence of coronary revascularization and heart failure as compared to other drugs like CCB, ACEI or ARB. 66 The evidence from the SHEP study emphasizes the value of a low-dose thiazide-type drug as initial therapy for isolated systolic hypertension in older patients. 67 Clinical trial data also indicate that diuretics are generally well tolerated [14-16].

β-Blockers

β-drugs are decrease cardiac output and the slowing of heart rate and were originally thought to be of clinical importance, particularly in hypertensive patients with tachycardia. But, at the same time, peripheral resistance is increased slightly and sodium re absorption by the kidney is increased. The ability of β-blockers to inhibit activity of the RAS by reducing the release of renin from the juxtaglomerular cells of the kidney may contribute to their blood pressure lowering effects, especially in patients with medium or high levels of plasma renin activity. 69 Over time, they became widely accepted for the treatment of hypertension, and one of the reasons for the acceptance of this drug class by clinicians was that these agents appeared to be better tolerated than many of the drugs previously available for treating hypertension [17].

Angiotensin-converting enzyme Inhibitors, angiotensin receptor antagonists and renin inhibitors Inhibitors of the renin-angiotensin system (RAS), including ACE-inhibitors, ARBs and now direct rennin inhibitor (DRI) are commonly used in the treatment of hypertension. ACE-inhibitors modulate blood pressure by inhibiting ACE mediated conversion of angiotensin I to angiotensin II. ARBs modulate blood pressure by inhibiting the activation of the AT1 receptor by angiotensin II. [18]. Aliskiren, a direct renin inhibitor, is the first of a new class of antihypertensive drugs that block the RAS further upstream. Its antihypertensive effect, safety, and tolerability are comparable with ARBs and ACE inhibitors; however, its long-term data is awaited [19].

Calcium channel blockers CCBs which include both dihydropyridines (DHPs) e.g., nifedipine and amlodipine and non-dihydropyridines, like verapamil and diltiazem, are among the most widely prescribed agents for the management of essential hypertension. Several large outcome risk trials and comprehensive meta-analyses have found that CCBs reduce the cardiovascular morbidity and mortality associated with uncontrolled hypertension, including stroke. [20] Conditions favoring the choice of a DHP CCB for hypertension include: advanced age, isolated systolic hypertension, angina pectoris, peripheral vascular disease, carotid atherosclerosis, and pregnancy. Diltiazem or verapamil is considered for use in patients with angina pectoris or supraventricular tachycardia.

Alpha-1 receptor antagonist Α1-adrenergic blocking drugs are effective in reducing blood pressure and do so in a fashion comparable to most other antihypertensive drug classes. Initially, for many years α1-adrenergic antagonists had been considered suitable initial drugs for uncomplicated early-stage hypertension. But guidelines including the European Society of Hypertension/European Society of Cardiology and the authors of the JNC 7 no longer include α1-adrenergic antagonists as initial agents for the treatment of hypertension [21].

TRPV1 antagonists Transient Receptor Potential Vanilloid Receptor type 1 is the latest site for the antihypertensive action. The endocannabinoid, anandamide, can have depressor effects and its production is upregulated in certain pathophysiological states. TRPV1 receptor has been implicated in the hypotensive effects of anandamide. Oleamide (cis-9 10 octadecenoamide) is a fatty acid primary amide, which was originally derived from sleep-deprived cats and shares structural similarities with anandamide [22-26].

Trials of Hypertension Prevention Collaborative Research Group, Effects of weight loss and sodium reduction intervention on blood pressure and hypertension incidence in overweight people with high-normal blood pressure: the Trials of Hypertension Prevention, Phase II. Arch. Intern. 

Table : Naturally occurring medicinal herbs having hypotensive/antihypertensive potential

Plant NameFamily & Common NameReference
Agathosma betulinaRutaceae; Common name: Buchu[27]
Allium sativumAlliaceae/Liliaceae; Common name: Garlic[28]
Annona muricataAnnonaceae; Common name: Prickly Custard Apple[29]
Apium graveolensApiaceae; Common name: Celery[27]
Aristolochia manshuriensisAristolochiaceae; Common name: Guan Mu Tong[30]
Artocarpus altilisMoraceae; Common name: Breadfruit[29]
Avena sativaPoaceae/Gramineae; Common names: Dietary Fiber, Green Oat[32]
Blond psylliumPlantaginaceae; Common name: Indian Plantago[31]
Camellia sinensisTheaceae; Common name: Tea[33]
Capparis cartilagineaCapparaceae; Common name: Lasaf[34]
Carum copticumUmbelliferae; Common name: Ajwain[35]
Cassia absusCaesalpiniaceae; Common name: Chaksu[36]
Cassia occidentalisCaesalpiniaceae; Common name: Coffee Weed[37]
Castanospermum australFabaceae; Common name: Black Bean[38]
Coleus forskohliiLamiaceae; Common name: Karpurvali[39]
Crataegus pinnatifidaRosaceae; Common name: Chinese Hawthorn[40]
Crinum glaucumAmaryllidaceae; Common name: River Lily/Swamp Lily[41]
Cuscuta reflexaCuscutaceae; Common name: Giant Dodder[42]
Daucus carotaUmbelliferae; Common name: Carrot[43]
Desmodium styracifoliumLeguminosae; Common name: Osbeck[44]
Fuchsia magellanicaOnagraceae; Common names: Hardy Fuchsia, Chiko, Tilco[45]
Glycine maxFabaceae; Common name: Soybean[46]
Gossypium barbadenseMalvaceae; Common name: Roselle[47]
Hibiscus sabdariffaMalvaceae; Common name: Roselle[48]
Lavandula stoechasLamiaceae; Common name: French Lavender[49]
Lepidium latifoliumCruciferae; Common name: Rompepiedra/Stone Breaker[50]
Linum usitatissimumLinaceae; Common names: Linseed, Flaxseed[51]
Lumnitzera racemosaCombretaceae; Common name: Black Mangrove[52]
Lycopersicon esculentumSolanaceae; Common name: Tomato[53]
Moringa oleiferaMoringaceae; Common name: Murungai[54]
Musanga cecropiodesCecropiaceae; Common names: Umbrella Tree, Cork Wood[55]
Ocimum basilicumLamiaceae; Common name: Basil[56]
Peganum harmalaNitrariaceae; Common name: Harmal[57]
Phyllanthus amarusEuphorbiaceae; Common name: Nela Nelli[58]
Pinus pinasterPinaceae; Common name: Maritime Pine[59]
Pueraria lobataFabaceae; Common name: Kudzu[60]
Punica granatumLythraceae; Common name: Pomegranate[61]
Raphanus sativusCruciferae; Common name: Radish[62]
Rauwolfia serpentinaApocynaceae; Common name: Rauwolfia[63]
Rhaptopetalum coriaceumScytopetalaceae[64]
Sesamum indicumPedaliaceae; Common name: Sesame[65]
Solanum sisymbriifoliumSolanaceae; Common names: Sticky Nightshade, Wild Tomato[66]
Theobroma cacaoMalvaceae; Common names: Chocolate, Cocoa Bean, Cocoa Butter[67]
Triticum aestivumPoaceae/Gramineae; Common names: Bran, Wheat Bran[68]
Uncaria rhynchophyllaRubiaceae; Common name: Cat's Claw Herb[69]
Viscum albumSantalaceae; Common name: Mistletoe[70]
Vitex donianaVerbenaceae; Common name: Black Plum[71]
Zingiber officinaleZingiberaceae; Common name: Ginger[27]

 

Human trials for hypotensive effect of ginger have been few and generally used a low dose with inconclusive results. The renewed interest in the search for new drugs from natural sources, especially from plant sources, has gained global attention during the last two decades. The tropical rain forests have become an important point of this activity, primarily due to the rich biodiversity they harbor, which promises a high diversity of chemicals with the potential novel structures. However, of this rich biodiversity, only a small portion has been studied for its medicinal potential. Thus, natural plants and herbs can be our source of drugs, with fewer side effects and better bioavailability for treatment of HTN in future.

Medicinal plants have been recognized as being effective in controlling and treating HTN. A small number of traditionally used plants have been confirmed precisely through animal studies and clinical trials, but the detailed mechanisms of action of these plants are still unknown. Medicinal plants are unsuccessful in attaining the anticipated scale due to a shortage of scientific data on their safety and efficiency. Thus, systematic validation studies are required [72-80]. Hypertension is a most common life style disease in India. Most of peoples are suffering hypertension and diabetic both of diseases, taking both type of drug, those peoples require alerting the fitness of body and the involved exercise, meditation, herbs, low diet and nutraceutical for the management diabetic syndrome [81-84].

14. Conclusion

Herbal plant therapy offers a possible substitute or addition to traditional treatment for hypertension.  Numerous medicinal plants contain bioactive substances such alkaloids, flavonoids, terpenoids, tannins, and saponins that work through mechanisms like diuresis, vasodilation, antioxidation, and renin-angiotensin system regulation to reduce hypertension. Herbal treatments are useful for long-term care since they frequently have fewer adverse effects and a more holistic effect than synthetic pharmaceuticals.  Nevertheless, there are still issues with safety, clinical validation, dosage adjustment, and standardization despite their potential. The goal of future research should be to create evidence-based, standardized, and efficient herbal compositions by fusing traditional knowledge with contemporary pharmacological investigations.  When used responsibly and backed by scientific evidence, herbal plants have the potential to significantly reduce the worldwide burden of hypertension and enhance patient quality of life.

15. Top of Form

Top of Form

Acknowledgement

We express our sincere gratitude to all authors contributed to the completion of this paper.

16. Conflict Of Interest 

No authors declared Conflict of Interest.

17. References

  1. Chen-Yi Wu, Hsiao-Yun Hu, Yiing-Jenq Chou, Nicole Huang,Yi-Chang Chou, MS, and Chung-Pin Li. High blood pressure and all-cause and cardiovascular disease mortalities in community-dwelling older adults. 2015; 94(47):1-10.
  2. https://my.clevelandclinic.org
  3. Samuel M. Zuber, Vitaly Kantorovich. Hypertension in Pheochromocytoma: Characteristics and Treatment. Endocrinol Metab Clin North Am. 2011; 40(2): 295-311.
  4. https://www.who.int
  5. https://www.ucsfhealth.org
  6. National High Blood Pressure Education Program. The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. Bethesda, MD: National Heart, Lung, and Blood Institute; 2003.
  7. Vasan RS, Beiser A, Seshadri S, Larson MG, Kannel WB, D’ Agostino RB, et al. Residual lifetime risk for developing hypertension in middle-aged women and men: the Framingham Heart Study. JAMA. 2002;287(8):1003-1010.
  8. Benjamin EJ, Muntner P, Alonso A, Bittencourt MS, Callaway CW, Carson AP, et al. Heart disease and stroke statistics 2019 update: a report from the American Heart Association. Circulation. 2019;139(10):e1-e473. 
  9. Daniel Santos; Mandip S. Dhamoo. Trends in Antihypertensive Medication Use Among Individuals With a History of Stroke and Hypertension, 2005 to 2016. JAMA Neurology. 2020;77(11):1382-11389.
  10. Feldman RD, Hussain Y, Kuyper LM, McAlister FA, Padwal RS, Tobe SW. Intraclass differences among antihypertensive drugs. Annu Rev Pharmacol Toxicol. 2015; 55:333-52.
  11. Lydia A. Bazzano, Torrance Green, Teresa N. Harrison, and Kristi Reynolds. Dietary Approaches to Prevent Hypertension. Curr Hypertens Rep. 2013 Dec; 15(6): 694-702.
  12. World Health Organization–International Society of Hypertension guidelines for the management of hypertension. Guidelines Subcommittee. J Hypertens.1999; 17:151–183.
  13. 13. Seamus P. Whelton,   Ashley Chin, MA,   Xue Xin,  Jiang He. Effect of Aerobic Exercise on Blood Pressure. Ann. Intern. Med., 2002, 136, 493-503.
  14. ALLHAT Collaborative Research Group. Major outcomes in high-risk hypertensive patients randomized to angiotensin-converting enzyme inhibitor or calcium channel blocker vs diuretic: The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT). JAMA, 2002, 288, 2981-2997.
  15. Kostis, J. B., Wilson, A. C., Freudenberger, R. S., Cosgrove, N. M., Pressel, S. L., Davis, B. R., Am. J. Cardiol., 2005, 95, 29-35.
  16. Materson, B. J., Reda, D. J., Cushman, W. C., Massie, B. M., Freis, E. D., Kochar, M. S., Hamburger, R. J., Fye, C., Lakshman, R., Gottdiener, J., Ramirez, E. A. and Henderson, W. G., New Engl. J. Med., 1993, 328, 914-921.
  17. Weber, M. A. Bakris, G. L., Giles, T. D., Messerli, F. H. Clinical practice guidelines for the management of hypertension in the community: a statement by the American Society of Hypertension and the International Society of Hypertension. J. Clin. Hypertens., 2008, 10, 234–238.
  18. Ram, C. V. S. Angiotensin Receptor Blockers: Current Status and Future ProspectsAm. J. Med., 2008, 121, 656–663.
  19. Gradman, A. H., Schmieder, R. E., Lins, R. L. Nussberger. Aliskiren, a novel orally effective renin inhibitor, provides dose-dependent antihypertensive efficacy and placebo-like tolerability in hypertensive patients. J., Chiang, Y., Bedigian, M. P., Circulation, 2005, 111, 1012–1018.
  20. Basile, J. The Role of Existing and Newer Calcium Channel Blockers in the Treatment of Hypertension. J. Clin. Hypertens., 2004, 6, 621–631.
  21. Iqbal, M. Severe scrub typhus infection: Clinical features, diagnostic challenges and management. Indian J. Clin. Med., 2011, 2, 1–17.
  22. Ho, W. S. V., Gardiner, S. M. Acute hypertension reveals depressor and vasodilator effects of cannabinoids in conscious rats. Br. J. Pharmacol., 2009,156, 94–104.
  23. Batkai, S., Pacher, P., Osei-Hyiaman, D., Radaeva, S., Liu, J., Harvey-White, J., Offertaler, L., Mackie, K., Rudd, M. A., Bukoski, R. D., Kunos, G. Endocannabinoids Acting at Cannabinoid-1 Receptors Regulate Cardiovascular Function in Hypertension. Circulation, 2004, 110, 1996-2002.
  24. Lake, K. D., Martin, B. R., Kunos, G., Varga, K. Cardiovascular Effects of Anandamide in Anesthetized and Conscious Normotensive and Hypertensive Rats. Hypertension, 1997, 29, 1204-1210.
  25. Wang, Y. P., Kaminski, N. E., Wang, D. H. Endocannabinoid Regulates Blood Pressure via Activation of the Transient Receptor Potential Vanilloid Type 1 in Wistar Rats Fed a High-Salt Diet. J. Pharmacol. Exp. Ther., 2007, 321, 763-769.
  26. Cravatt, B. F., Prosperogarcia, O., Siuzdak, G., Gilula, N. B., Henriksen, S. J., Boger, D. L., Lerner, R. A. Chemical Characterization of a Family of Brain Lipids That Induce Sleep. Science, 1995, 268, 1506-1509.
  27. Jaarin K, Foong WD, Yeoh MH, Kamarul ZY, Qodriyah HM, Azman A, et al. Mechanisms of the antihypertensive effects of Nigella sativa oil in L-NAME-induced hypertensive rats. Clinics (Sao Paulo) 2015;70(11):751-7. doi: 10.6061/ clinics/2015(11)07
  28. Ladeji O, Udoh FV, Okoye ZS. Activity of aqueous extract of the bark of Vitex doniana on uterine muscle response to drugs. Phytother Res 2005;19(9):804-6. doi: 10.1002/ ptr.1588
  29. Lee YJ, Choi DH, Cho GH, Kim JS, Kang DG, Lee HS. Arctium lappa ameliorates endothelial dysfunction in rats fed with high fat/cholesterol diets. BMC Complement Altern Med 2012;12:116. doi: 10.1186/1472-6882-12-116
  30. Verma SK, Jain V, Katewa SS. Blood pressure lowering, fibrinolysis enhancing and antioxidant activities of cardamom (Elettaria cardamomum). Indian J Biochem Biophys 2009;46(6):503-6.
  31. Lamba A, Oakes AK, Roberts L, Deprele S. The Effects of Crude and Purified Cat’s Claw Extracts on Viability and Toxicity of HeLa Cells. Southern California Conference for Undergraduate Research (SCCUR); 2018.
  32. Siska S, Mun Im A, Bahtiar A, Suyatna FD. Effect of Apium graveolens extract administration on the pharmacokinetics of captopril in the plasma of rats. Sci Pharm 2018;86(1):6. doi: 10.3390/scipharm86010006
  33. Ahmad S, Hassan A, Abbasi WM, Rehman T. Phytochemistry and pharmacological potential of Cassia absus - a review. J Pharm Pharmacol 2018;70(1):27-41. doi: 10.1111/jphp.12816
  34. Cho YH, Ku CR, Hong ZY, Heo JH, Kim EH, Choi DH, et al. Therapeutic effects of water soluble danshen extracts on atherosclerosis. Evid Based Complement Alternat Med 2013;2013:623639. doi: 10.1155/2013/623639
  35. Jiang B, Li D, Deng Y, Teng F, Chen J, Xue S, et al. Salvianolic acid A, a novel matrix metalloproteinase-9 inhibitor, prevents cardiac remodeling in spontaneously hypertensive rats. PLoS One 2013;8(3):e59621. doi: 10.1371/journal. pone.0059621
  36. Nyadjeu P, Nguelefack-Mbuyo EP, Atsamo AD, Nguelefack TB, Dongmo AB, Kamanyi A. Acute and chronic antihypertensive effects of Cinnamomum zeylanicum stem bark methanol extract in L-NAME-induced hypertensive rats. BMC Complement Altern Med 2013;13:27. 
  37. Irondi AE, Olawuyi AD, Lawal BS, Boligon AA, Olasupo F, Olalekan SI. Comparative inhibitory effects of cocoa bean and cocoa pod husk extracts on enzymes associated with hyperuricemia and hypertension in vitro. Int Food Res J 2019;26(2):557-64.
  38. Ali M, Ansari SH, Ahmad S, Sanobar S, Hussain A, Khan SA, et al. Phytochemical and pharmacological approaches of traditional alternate Cassia occidentalis L. In: Ozturk M, Hakeem KR, eds. Plant and Human Health, Volume 3: Pharmacology and Therapeutic Uses. Cham: Springer; 2019:321-41. 
  39. Ramkissoon JS, Mahomoodally MF, Ahmed N, Subratty AH. Antioxidant and anti-glycation activities correlates with phenolic composition of tropical medicinal herbs. Asian Pac J Trop Med 2013;6(7):561-9. doi: 10.1016/s1995- 7645(13)60097-8
  40. Wu TT, Tsai CW, Yao HT, Lii CK, Chen HW, Wu YL, et al. Suppressive effects of extracts from the aerial part of Coriandrum sativum L. on LPS-induced inflammatory responses in murine RAW 264.7 macrophages. J Sci Food Agric 2010;90(11):1846-54. 
  41. Cheraghi Niroumand M, Farzaei MH, Amin G. Medicinal properties of Peganum harmala L. in traditional Iranian medicine and modern phytotherapy: a review. J Tradit Chin Med 2015;35(1):104-9. doi: 10.1016/s0254-6272(15)30016
  42. Dang Y, Xu Y, Wu W, Li W, Sun Y, Yang J, et al. Tetrandrine suppresses lipopolysaccharide-induced microglial activation by inhibiting NF-κB and ERK signaling pathways in BV2 cells. PLoS One 2014;9(8):e102522. doi: 10.1371/ journal.pone.0102522
  43. Fan QL, Zhu YD, Huang WH, Qi Y, Guo BL. Two new acylated flavonol glycosides from the seeds of Lepidium sativum. Molecules 2014;19(8):11341-9. doi: 10.3390/ molecules190811341
  44. Shouk R, Abdou A, Shetty K, Sarkar D, Eid AH. Mechanisms underlying the antihypertensive effects of garlic bioactives. Nutr Res 2014;34(2):106-15. doi: 10.1016/j.
  45. nutres.2013.12.005
  46. Ashraf R, Khan RA, Ashraf I, Qureshi AA. Effects of Allium sativum (garlic) on systolic and diastolic blood pressure in patients with essential hypertension. Pak J Pharm Sci 2013;26(5):859-63.
  47. Vazquez-Prieto MA, Rodriguez Lanzi C, Lembo C, Galmarini CR, Miatello RM. Garlic and onion attenuates vascular inflammation and oxidative stress in fructose-fed rats. J Nutr Metab 2011;2011:475216. doi: 10.1155/2011/475216
  48. Ried K, Frank OR, Stocks NP. Aged garlic extract reduces blood pressure in hypertensives: a dose-response trial. Eur J Clin Nutr 2013;67(1):64-70. doi: 10.1038/ejcn.2012.178
  49. Rhee MY, Cho B, Kim KI, Kim J, Kim MK, Lee EK, et al. Blood pressure lowering effect of Korea ginseng derived ginseol K-g1. Am J Chin Med 2014;42(3):605-18. doi: 10.1142/s0192415x14500396
  50. Jovanovski E, Bateman EA, Bhardwaj J, Fairgrieve C, Mucalo I, Jenkins AL, et al. Effect of Rg3-enriched Korean red ginseng (Panax ginseng) on arterial stiffness and blood pressure in healthy individuals: a randomized controlled trial. J Am Soc Hypertens 2014;8(8):537-41. 
  51. Lan J, Zhao Y, Dong F, Yan Z, Zheng W, Fan J, et al. Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension. J Ethnopharmacol 2015;161:69-81. doi: 10.1016/j.jep.2014.09.049
  52. Wan X, Chen X, Liu L, Zhao Y, Huang WJ, Zhang Q, et al. Berberine ameliorates chronic kidney injury caused by atherosclerotic renovascular disease through the suppression of NFκB signaling pathway in rats. PLoS One 2013;8(3):e59794. doi: 10.1371/journal.pone.0059794
  53. Maulik SK, Banerjee SK. Uses of herbals in cardiac diseases: priority of evidence over belief. In: Mukherjee PK, ed. Evidence-Based Validation of Herbal Medicine. Boston: Elsevier; 2015. p. 515-29. doi: 10.1016/b978-0-12-800874- 4.00024-6
  54. Asher GN, Viera AJ, Weaver MA, Dominik R, Caughey M, Hinderliter AL. Effect of hawthorn standardized extract on flow mediated dilation in prehypertensive and mildly hypertensive adults: a randomized, controlled crossover trial. BMC Complement Altern Med 2012;12:26. doi: 10.1186/1472-6882-12-26
  55. Baradaran A, Nasri H, Rafieian-Kopaei M. Oxidative stress and hypertension: possibility of hypertension therapy with antioxidants. J Res Med Sci 2014;19(4):358-67.
  56. Lobay D. Rauwolfia in the treatment of hypertension. Integr Med (Encinitas) 2015;14(3):40-6.
  57. Bahem R, Hoffmann A, Azonpi A, Caballero-George C, Vanderheyden P. Modulation of calcium signaling of angiotensin AT1, endothelin ETA, and ETB receptors by silibinin, quercetin, crocin, diallyl sulfides, and ginsenoside Rb1. Planta Med 2015;81(8):670-8. doi: 10.1055/s-0034-1383408
  58. Sharma P, Sanadhya D. The king of bitters,”Andrographis paniculata”: a plant with multiple medicinal properties. J Plant Sci Res 2017;33(1):117-25.
  59. Awang K, Abdullah NH, Hadi AH, Fong YS. Cardiovascular activity of labdane diterpenes from Andrographis paniculata in isolated rat hearts. J Biomed Biotechnol 2012;2012:876458.
  60. Chen C, Chen C, Wang Z, Wang L, Yang L, Ding M, et al. Puerarin induces mitochondria-dependent apoptosis in hypoxic human pulmonary arterial smooth muscle cells. PLoS One 2012;7(3):e34181. 
  61. Devi RC, Sim SM, Ismail R. Effect of Cymbopogon citrates and citral on vascular smooth muscle of the isolated thoracic rat aorta. Evid Based Complement Alternat Med 2012;2012:539475. 
  62. Francisco V, Costa G, Figueirinha A, Marques C, Pereira P, Miguel Neves B, et al. Anti-inflammatory activity of Cymbopogon citratus leaves infusion via proteasome and nuclear factor-κB pathway inhibition: contribution of chlorogenic acid. J Ethnopharmacol 2013;148(1):126-34. doi: 10.1016/j.jep.2013.03.077
  63. Mishra R, Sharma S, Sharma RS, Singh S, Sardesai MM, Sharma S, et al. Viscum articulatum Burm. f. aqueous extract exerts antiproliferative effect and induces cell cycle arrest and apoptosis in leukemia cells. J Ethnopharmacol 2018;219:91-102. 
  64. Kamohara S, Terasaki Y, Horikoshi I, Sunayama S. Safety of a Coleus forskohlii formulation in healthy volunteers. Personalized Medicine Universe 2015;4:63-5. doi: 10.1016/j. pmu.2015.01.001
  65. Valls RM, Llauradó E, Fernández-Castillejo S, Puiggrós F, Solà R, Arola L, et al. Effects of low molecular weight procyanidin rich extract from French maritime pine bark on cardiovascular disease risk factors in stage-1 hypertensive subjects: randomized, double-blind, crossover, placebo-controlled intervention trial. Phytomedicine 2016;23(12):1451-61. 
  66. Carre G, Ouedraogo M, Magaud C, Carreyre H, Becq F, Bois P, et al. Vasorelaxation induced by dodoneine is mediated by calcium channels blockade and carbonic anhydrase inhibition on vascular smooth muscle cells. J Ethnopharmacol 2015;169:8-17. doi: 10.1016/j. jep.2015.03.037
  67. Aekthammarat D, Pannangpetch P, Tangsucharit P. Moringa oleifera leaf extract lowers high blood pressure by alleviating vascular dysfunction and decreasing oxidative stress in L-NAME hypertensive rats. Phytomedicine 2019;54:9-16. 
  68. Brankovic S, Radenkovic M, Kitic D, Veljkovic S, Ivetic V, Pavlovic D, et al. Comparison of the hypotensive and bradycardic activity of ginkgo, garlic, and onion extracts. Clin Exp Hypertens 2011;33(2):95-9. 
  69. Poh TF, Ng HK, Hoe SZ, Lam SK. Gynura procumbens causes vasodilation by inhibiting angiotensin II and enhancing bradykinin actions. J Cardiovasc Pharmacol 2013;61(5):378-84. 
  70. Ng HK, Poh TF, Lam SK, Hoe SZ. Potassium channel openers and prostacyclin play a crucial role in mediating the vasorelaxant activity of Gynura procumbens. BMC Complement Altern Med 2013;13:188. 
  71. Asgary S, Hashemi M, Goli-Malekabadi N, Keshvari M. The effects of acute consumption of pomegranate juice (Punica granatum L.) on decrease of blood pressure, inflammation, and improvement of vascular function in patients with hypertension: a clinical trial. J Shahrekord Univ Med Sci 2015;16(6):84-91.
  72. de CC Pinto N, Campos LM, Evangelista ACS, Lemos ASO, Silva TP, Melo RCN, et al. Antimicrobial Annona muricata L. (soursop) extract targets the cell membranes of gram-positive and gram-negative bacteria. Ind Crops Prod 2017;107:332-40. 
  73. Kook SH, Choi KC, Lee YH, Cho HK, Lee JC. Raphanus sativus L. seeds prevent LPS-stimulated inflammatory response through negative regulation of the p38 MAPKNF-κB pathway. Int Immunopharmacol 2014;23(2):726-34. 
  74. Shukla AK, Tiwari A, Yadav VK, Yadav VP, Kanaujia KA, Mishra MK, Sharma M, Verma G. Preliminary phytochemical, isolation, characterization, antioxidant, and antimicrobial activity assessments of Achyranthes aspera L. Biosci Biotechnol Res Asia. 2025;22(1):401-10.
  75. Shukla AK, Kanaujia KA, Yadav VK, Verma M, Jaiswal A, Gupta V. Expert systems in preformulation and formulation development with special reference to SeDeM system: an innovative, problem solving, intelligent and optimization algorithm tool. Curr Indian Sci. 2024;(2):1-12. doi:10.2174/012210299X338978241015155050.
  76. Shukla AK, Kumar M, Bishnoi RS, Jain CP. Applications of tamarind seed polysaccharide-based copolymers in controlled drug delivery: an overview. Asian J Pharm Pharmacol. 2018;4(1):23-30.
  77. Shukla AK, Bishnoi RS, Kumar M, Jain CP, Tiwari R, Jain R. Bioavailability enhancement and dissolution rate of poor water-soluble drug by solid dispersion technique. Indian J Novel Drug Deliv. 2020;12(4):201-7.
  78. Shukla AK, Singh SK, Mishra SP, Sarthi AS, Dewangan E, Bharti VR, Sonkar SK. Development and characterization of natural polymer based nifedipine sustained release matrix tablet. J Pharm Negat Results. 2022;13(8):3663-8. doi:10.47750/pnr.2022.13.S08.454.
  79. Shukla AK, Yadav VK, Kumar P, Tiwari A, Tiwari J. Use of natural gum in poorly water-soluble drug solid dispersion and solubility enhancement. Res J Pharm Technol. 2025;18(8):3995-4000. doi:10.52711/0974-360X.2025.00574.
  80. Dubey RS, Naidu MA, Shukla AK, Shukla AK. Application of bioactive molecules in the treatment and management of type-1 diabetic disease: an overview. Sci Temper. 2022;13(2):264-80. doi:10.58414/SCIENTIFICTEMPER.2022.13.2.40.
  81. Dubey RS, Verma NK, Shukla AK, Naidu MA. Diabetes mellitus a report on antidiabetic medicinal plants and their potent bioactive molecules. J Med Pharm Allied Sci. 2021;10(3):2949-60. doi:10.22270/jmpas.V10I3.1414.
  82. Shukla AK, Bishnoi RS, Kumar M, Jain CP. Development of natural and modified gum based sustained-release film-coated tablets containing poorly water-soluble drug. Asian J Pharm Clin Res. 2019;12(3):266-71.
  83. Shukla AK, Bishnoi RS, Kumar M, Jain CP. Development of natural gum based sustained release tablets of propranolol hydrochloride. Res J Pharm Technol. 2019;12(7):3295-300.
  84. Shukla AK, Bishnoi RS, Kumar M, Jain CP. Isolation and characterization of natural and modified seed gum. Asian J Pharm Pharmacol. 2019;5(2):409-18.
  85. Tiwari V, Sharma M, Yadav VK, Kanaujia KA, Yadav VP, Bharti V, Yadav MK. Solubility enhancement and estimation of paracetamol and domperidone by hydrotropic agents. Biochem Cell Arch. 2024;24(2):2783-93. doi:10.51470/bca.2024.24.2.0000.