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  • Evaluation of Pharmacological Effects of Bauhinia Vaeriegata Linn on Non-Alcoholic Fatty Liver Disease in High-Fat Diet-Induced Experimental Rats

  • 1Research Scholar, Maharishi Arvind Institute of Pharmacy, Jaipur, Rajasthan
    2Associate Professor, Maharishi Arvind Institute of Pharmacy, Jaipur, Rajasthan
    3Principal, Maharishi Arvind Institute of Pharmacy, Jaipur, Rajasthan

Abstract

Non-alcoholic fatty liver disease (NAFLD) is one of the most prevalent chronic liver disorders worldwide and is strongly associated with obesity, insulin resistance, dyslipidemia, and type 2 diabetes mellitus. The present study was designed to evaluate the therapeutic potential of methanolic extract of Bauhinia variegata (MBV) against high-fat diet (HFD)-induced NAFLD in experimental rats. Bauhinia variegata is presence of phytoconstituents such as alkaloids, flavonoids, tannins, saponins, glycosides, and phenolic compounds. The powdered plant material was extracted using methanol in a Soxhlet apparatus. NAFLD was induced in rats by administration of a high-fat diet for 35 days. Animals were divided into five groups: normal control, disease control, standard control (Atorvastatin 20 mg/kg), test group I (MBV 200 mg/kg), and test group II (MBV 400 mg/kg). Biochemical parameters including liver function tests (ALT, AST, ALP), lipid profile (HDL, LDL, total cholesterol, triglycerides), body weight, food intake, water intake, and histopathological analysis of liver tissue were evaluated. The findings suggest that Bauhinia variegata possesses significant hepatoprotective and antihyperlipidemic activity against HFD-induced NAFLD, possibly due to its antioxidant and anti-inflammatory properties. Thus, the plant extract may serve as a promising natural therapeutic agent for the management of NAFLD.

Keywords

Fatty Liver, High Fat Diet, Bauhinia Vaeriegata, Herbal Plant

Introduction

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Non-alcoholic fatty liver disease (NAFLD) is a prevalent and increasingly significant liver disorder characterized by the accumulation of fat in the liver (steatosis) in individuals who consume little or no alcohol.1 Non-alcoholic fatty liver disease (NAFLD) has evolved from a relatively unknown disease to the most common cause of chronic liver disease worldwide.2 Currently, a consensus defines NAFLD as an umbrella term for a range of diseases in which steatosis is present in more than 5% of hepatocytes with metabolic risk factors (especially obesity and type 2 diabetes), excluding excessive alcohol consumption or other chronic liver disease.3 NAFLD is fast becoming one of the most common causes of chronic liver disease worldwide, and is now a major cause of liver-related morbidity and mortality. The symptoms are usually associated with features of metabolic syndrome, such as obesity, dyslipidemia, type 2 diabetes and hypertension. However, the pathogenesis of NAFLD is unknown, and this has become a hindrance to the treatment of NAFLD.4

Insulin resistance (in body and adipose tissue) increases the release of free fatty acids (FFA) from adipose tissue. These excess FFAs enter the liver, leading to triglyceride accumulation → this causes fatty liver (steatosis).5 Insulin resistance also increases SREBP-1c and ChREBP, which stimulate more fat synthesis in the liver, worsening fat accumulation. As fat builds up, the liver becomes insulin resistant, further increasing glucose and insulin levels → a vicious cycle.6 Excess liver fat generates inflammation and oxidative stress causing: Activation of hepatic stellate cells and Hepatocellular injury and NAFLD.7 Alkaloids present in Bauhinia variegate linn  shows Wound healing, inflammation, Antioxidant, liver disorders, stomach disorders, Jaundice. Major constituents are Carbohydrates, glycosides, alkaloids, Saponins, Tannins, Flavonoids, Phenolic compounds and traditional uses8,9: Pharmacological actions: Hepatoprotective, Anti-diabetic, wound healing, anti-diarrhoeal, anti-ulcer activity.10 Therefore to investigate the therapeutic effects of Bauhinia variegate (Kachnar) extract in ameliorating non-alcoholic fatty liver disease (NAFLD) in high-fat diet- induced experimental rats. To explore the histopathological changes in liver tissue to determine the extent of liver damage and the potential hepatoprotective effects of bauhinia  variegatea..

Material and Methods

Bauhinia variegata were collected and dried. The powdered plant material of Bauhinia variegatawas packed into a thimble and placed in the Soxhlet apparatus, after which methanol was used as the extracting solvent.

Experimental method:

All the animals used in the experiment were approved by the Institutional Animal Ethics Committee (IAEC).

Table 1: Experimental Design

Group n=6

Dose

Duration

Normal control

Saline p.o.

49 days

Disease control

High fat diet

(HFD)10ml/kg orally

49 days

Standard control

Atorvastatin 20mg/kg+HFD

orally

HFD-1-35 days, Atorvastatin-35-

49days

Test- 1

MBV 200mg/kg

HFD-1-35 days,

MBV-35-49days

Test -2

MBV 400mg/kg

HFD-1-35 day

MBV-35-49days

 

The disease model wiere induced in animals by administering a high-fat diet. The diet were carefully prepared by combining specific ingredients, including corn oil (400 g), sucrose (150 g), total milk powder (80 g), lard (100 g), egg yolk (200 g), sodium deoxycholate (10 g), tween 80 (36.4 g), propylene glycol (31.1 g), vitamin mixture (2.5 g), cooking salt (10 g), mineral mixture (1.5 g), and distilled water (300 mL). All components were thoroughly mixed to ensure uniformity before being provided to the test animals.

Evaluation Parameter:

Sr.No.

Evaluation Parameter

1.

Daily parameter- Food intake, water intake

2.

Weekly parameter- Body weight

3.

Biochemical parameter-

Liver function test: ALT, AST, ALP

Lipid profile test: HDL, LDL, TG, TC

4.

Histopathological analysis of liver tissue- H&E Staining

 

Results And Discussion:

  1. EFFECT OF B.VARIEGATA ON LIPID PROFILE OF ANIMALS:
   

 

The levels of LDL was significantly increased in the disease group while HDL is decreased in disease group compared to the normal group. The levels of total cholesterol and truglycerides was significantly increased in the disease group compared to the normal group. Statistical significance denoted as (*-p< 0.05, **-p<0.01 and ***-p<0.001 compared to the disease control group.

2. EFFECT OF B.VARIEGATA ON LIVER ENZYME LEVEL OF ANIMALS:

               

 

            

 

 

 

The levels of ALP and ALT was significantly increased in the disease group compared to the normal group.  The levels of AST and total bilirubin was significantly increased in the disease group compared to the normal group while level of total protein was decersead in the disease group compared to the nnormal group. Statistical significance denoted as (*-p< 0.05, **-p<0.01 and ***-p<0.001 compared to the disease control group.

CONCLUSION

High-fat diet feeding resulted in metabolic disturbances such as increased body weight, altered lipid profile, elevated liver enzyme levels, and reduced antioxidant enzyme activity, indicating successful induction of NAFLD. However, treatment with the plant extract significantly improved these parameters. Therefore, the results of this study suggest that the plant extract has promising therapeutic potential in the prevention and management of NAFLD. However, further studies are required to elucidate the exact molecular mechanisms responsible for its protective effects and to evaluate its safety and efficacy in clinical settings. In conclusion, the plant extract may serve as a potential natural therapeutic agent for the management of non-alcoholic fatty liver disease.

REFERENCES

  1. Pouwels S, Sakran N, Graham Y, Leal A, Pintar T, Yang W, et al. Non-alcoholic fatty liver disease (NAFLD): a review of pathophysiology, clinical management and effects of weight loss. BMC Endocrine Disorders [Internet]. 2022 Mar 14;22(1).
  2. Ahmed A, Wong RJ, Harrison SA. Nonalcoholic fatty liver disease review: diagnosis, treatment, and outcomes. Clin Gastroenterol Hepatol. 2015;13(12):2062–70.
  3. Machado MV, Diehl AM. Pathogenesis of nonalcoholic Steatohepatitis. Gastroenterology. 2016;150(8):1769–77.
  4. Nasr P, Ignatova S, Kechagias S, Ekstedt M. Natural history of nonalcoholic fatty liver disease: a prospective follow-up study with serial biopsies. Hepatol Commun. 2018;2(2):199–210.
  5. Nasr P, Ignatova S, Kechagias S, Ekstedt M. Natural history of nonalcoholic fatty liver disease: a prospective follow-up study with serial biopsies. Hepatol Commun. 2018;2(2):199–210.
  6. Browning JD, Szczepaniak LS, Dobbins R, Nuremberg P, Horton JD, Cohen JC, et al. Prevalence of hepatic steatosis in an urban population in the United States: impact of ethnicity. Hepatology (Baltimore, Md). 2004;40(6):1387–95.
  7. RajKapoor B, Jayakar B, Murugesh N, Sakthisekaran D. Chemoprevention and cytotoxic effect of Bauhinia variegate against N-nitrosodiethylamine induced liver tumors and human cancer cell lines. J Ethnopharmacol 2006; 104: 407- 409
  8. Balamurugan G and Muralidharan P. Antiobesity effect of Bauhinia variegata bark extract on female rats fed on hypercaloric diet. Bangladesh J Pharmacol 2010; 5: 8- 12.
  9. Sharma RK, Rajani GP, Sharma V, Komala N. Effect of ethanolic and aqueous extracts of Bauhinia variegata Linn. on gentamicin-induced nephrotoxicity in rats. Ind J Pharm Edu Res 2011 ; 45(2):192-198.
  10. Surendra BH and Alpana R. Hepatoprotective properties of Bauhinia variegata bark extract. The Pharmaceutical Society of Japan 2007; 127(9): 1503-1507.

Reference

  1. Pouwels S, Sakran N, Graham Y, Leal A, Pintar T, Yang W, et al. Non-alcoholic fatty liver disease (NAFLD): a review of pathophysiology, clinical management and effects of weight loss. BMC Endocrine Disorders [Internet]. 2022 Mar 14;22(1).
  2. Ahmed A, Wong RJ, Harrison SA. Nonalcoholic fatty liver disease review: diagnosis, treatment, and outcomes. Clin Gastroenterol Hepatol. 2015;13(12):2062–70.
  3. Machado MV, Diehl AM. Pathogenesis of nonalcoholic Steatohepatitis. Gastroenterology. 2016;150(8):1769–77.
  4. Nasr P, Ignatova S, Kechagias S, Ekstedt M. Natural history of nonalcoholic fatty liver disease: a prospective follow-up study with serial biopsies. Hepatol Commun. 2018;2(2):199–210.
  5. Nasr P, Ignatova S, Kechagias S, Ekstedt M. Natural history of nonalcoholic fatty liver disease: a prospective follow-up study with serial biopsies. Hepatol Commun. 2018;2(2):199–210.
  6. Browning JD, Szczepaniak LS, Dobbins R, Nuremberg P, Horton JD, Cohen JC, et al. Prevalence of hepatic steatosis in an urban population in the United States: impact of ethnicity. Hepatology (Baltimore, Md). 2004;40(6):1387–95.
  7. RajKapoor B, Jayakar B, Murugesh N, Sakthisekaran D. Chemoprevention and cytotoxic effect of Bauhinia variegate against N-nitrosodiethylamine induced liver tumors and human cancer cell lines. J Ethnopharmacol 2006; 104: 407- 409
  8. Balamurugan G and Muralidharan P. Antiobesity effect of Bauhinia variegata bark extract on female rats fed on hypercaloric diet. Bangladesh J Pharmacol 2010; 5: 8- 12.
  9. Sharma RK, Rajani GP, Sharma V, Komala N. Effect of ethanolic and aqueous extracts of Bauhinia variegata Linn. on gentamicin-induced nephrotoxicity in rats. Ind J Pharm Edu Res 2011 ; 45(2):192-198.
  10. Surendra BH and Alpana R. Hepatoprotective properties of Bauhinia variegata bark extract. The Pharmaceutical Society of Japan 2007; 127(9): 1503-1507.

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Muskan Jain
Corresponding author

Maharishi Arvind Institute of Pharmacy, Jaipur, Rajasthan

Photo
Richa Agarwal
Co-author

Maharishi Arvind Institute of Pharmacy, Jaipur, Rajasthan

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Rajesh Asija
Co-author

Maharishi Arvind Institute of Pharmacy, Jaipur, Rajasthan

Muskan Jain, Richa Agarwal, Rajesh Asija, Evaluation of Pharmacological Effects of Bauhinia Vaeriegata Linn on Non Alcoholic Fatty Liver Disease in High-Fat Diet-Induced Experimental Rats, Int. J. of Pharm. Sci., 2026, Vol 4, Issue 5, 7421-7426. https://doi.org/10.5281/zenodo.20413747

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