Neuroprotective Effect of Boswellia serrata against 3-NP Induced Experimental Huntington’s Disease

Author:

Kumar Vinay1,Sharma Chanchal1,Taleuzzaman Mohamad2ORCID,Nagarajan Kandasamy3,Haque Anzarul4,Bhatia Mamta5,Khan Sumayya6ORCID,Salkini Mohamad Ayman7,Bhatt Pankaj8

Affiliation:

1. Department of Pharmacology, KIET Group of Institutions (KIET School of Pharmacy), Delhi-NCR, Ghaziabad-Meerut Road (NH-58), Ghaziabad, 201206 (UP), India

2. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Maulana Azad University, Village Bujhawar, Tehsil Luni, Jodhpur 342008, Rajasthan, India

3. Department of Pharmaceutical Chemistry, KIET Group of Institutions (KIET School of Pharmacy), Delhi-NCR, Ghaziabad-Meerut Road (NH-58), Ghaziabad, 201206 (UP), India

4. Department of Pharmaceutics, Buraydah College of Dentistry and Pharmacy, P.O. Box, 31717, Buraydah, Al-Qassim, Saudi Arabia

5. Department of Pharmacognosy, Faculty of Pharmacy, Maulana Azad University, Village Bujhawar, Tehsil Luni, Jodhpur 342008, Rajasthan, India

6. Department of Pharmacology, Faculty of Pharmacy, Maulana Azad University, Village Bujhawar, Tehsil Luni, Jodhpur 342008, Rajasthan, India

7. Department of Pharmacognosy, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Al Kharj 1194, Saudi Arabia

8. Department of Pharmaceutics, KIET Group of Institutions (KIET School of Pharmacy), Delhi-NCR, Ghaziabad- Meerut Road (NH-58), Ghaziabad, 201206 (UP), India

Abstract

Objectives: The study aimed to assess the neuroprotective effect of Boswellia serrata against 3-NP-induced experimental Huntington’s disease. Background: Previous studies have shown Boswellia to have sedative, analgesic, and anti-tumour effects. Boswellia serrata yields four pentacyclic triterpene acids and boswellic acid, a bioactive substance that prevents leukotriene biogenesis. Methods: The potential neuroprotective effect of Boswellia serrata against 3-nitro propionic acid (3-NP)-induced Huntington's disease (HD) was examined at oral doses of 45 mg/kg, 90 mg/kg, and 180 mg/kg. In this study, HD was induced by 3-NP at a dose of 10 mg/kg in Wistar rats. The study used 56 Wistar rats (8 per group) for biochemical (inflammatory markers, acetylcholinesterase activity) and behavioural (elevated plus maze, Y-maze, open-field, tail suspension tests, etc.) assessments. Additionally, a histological examination of the brain was carried out. In addition, the analysis of Boswellia serrata extract was performed by different analytical techniques, like UV spectrophotometer, FTIR, and HPLC methods. Results: In the brain, succinate dehydrogenase is a mitochondrial enzyme irreversibly inhibited by 3-NP. Administration of 3-NP resulted in HD with altered behavioural and motor changes in rats. Treatment with Boswellia serrata resulted in remarkable protection of rats against 3-NP-induced behaviour and motor deficits in a dose-dependent manner. Moreover, in rats administered with 3-NP, Boswellia serrata improved memory performance and lowered levels of inflammatory biomarkers. These results have also been supported by histopathological analysis. Acetyl-11-keto-p-boswellic acid was found to be the main active component of Boswellia serrata extract. Conclusion: Boswellia serrata at a dose of 180 mg/kg exhibited better protection compared to the other doses against HD induced by 3-NP. More detailed studies based on molecular targets are needed for the Boswellia serrata to transition from the bench to the bedside for use as an adjuvant in HD patients.

Publisher

Bentham Science Publishers Ltd.

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