Gemfibrozil and Nigella Sativa: Comparison

Research Article

Austin J Pharmacol Ther. 2019; 7(1).1109.

Gemfibrozil and Nigella Sativa: Comparison

Shah Murad1*, Durreshehwar Marwat2, Abdul Qudoos3 and M Arif4

1Professor of Pharmacology, IMDC, Pakistan

2AP Forensic Medicine at IMDC, Pakistan

3Assistant Professor of Pharmacology, FM&DC, Pakistan

4Assoc Professor of FM at IMDC, Pakistan

*Corresponding author: Shah Murad, HOD Pharmacology, Islamabad Medical College, Islamabad, Pakistan

Received: January 21, 2019; Accepted: February 25, 2019; Published: March 04, 2019

Abstract

Hyperlipidemia especially LDL-cholesterol may lead to development of coronary artery disease causing morbidity or mortality due to cardiac arrhythmias. Conventional hypolipidemic drugs have unwanted effects. Herbal therapy for Hyperlipidemia is getting attention due to their less frequent side effects. In this study we have compared hypolipidemic effects of Gemfibrozil with Nigella sativa. Seventy five hyperlipidemic patients from Jinnah Hospital Lahore were enrolled for study. After getting consent all patients were divided in three groups comprising 25 patients in each group. Group 1 was on Nigella sativa, group 2 was on Gemfibrozil and third group was on placebo therapy. They were advised to take drugs for two months. After completion of study pretreatment and post treatment values of LDL cholesterol were analyzed statistically. In Nigella sativa group LDL cholesterol decreased from 191.14±3.45 to 159.40±2.98 mg/dl, means 31.7 mg/dl LDL reduction was observed when compared with placebo group. In Gemfibrozil group of patients LDL cholesterol decreased from 197.77±3.91 mg/dl to 159.62±2.20 mg/dl, means LDL reduction in mean values was 38.2 mg/dl, when compared with placebo group. These changes are highly significant with p-values of ‹0.001. We concluded from this study that herbal medicine Nigella sativa is as effective as traditionally used hypolipidemic drug Gemfibrozil.

Introduction

Use of saturated fats cause LDL oxidation in systemic circulation and formation of atherosclerosis and may develop coronary artery disease [1,3-9]. In some cases, a blood clot may totally block the blood supply to the heart muscle, causing heart attack. If a blood vessel to the brain is blocked, usually from a blood clot, an ischemic stroke can result [2,10]. Hypolipidemic drugs can be used to treat hyperlidemia, CAD, heart arrhythmias and cardiac arrest. Allopathic drugs used to prevent or cure Hyperlipidemia include Statins, Fibrates, niacin and bile acid binding resins [3,8]. Gemfibrozil increases plasma HDL levels by stimulating their synthesis. Increased transport (turnover) of HDL induced by gemfibrozil may be significant in increasing tissue cholesterol removal in hyperlipidemic patients [4,7]. Furthermore, Fibrates treatment results in the formation of LDL with a higher affinity for the LDL receptor, which are thus catabolized more rapidly [5-7]. Nigella sativa or kalonji contains conjugated linoleic acid, thymoquinone, melanthin, nigilline, damascenine, and trans-anethole. Thymoquinone (TQ) extracted from Nigella sativa (kalonji) inhibits iron-dependent microsomal lipid peroxidation. Stimulation of polymorph nuclear leukocytes with thymoquinone works as protector against damaging effects of free redicles generated biochemically in human body [10].

Patients and Method

Research study design was single blind placebo-controlled, and was conducted at Jinnah Hospital, Lahore from February 2012 to July 2012. Seventy five hyperlipidemic patients were selected for research work. Written consent was taken from all patients. Specific Performa was designed for the research work. Seventy-five newly diagnosed primary hyperlipidemic patients were selected with age range from 18 to 70 years. Exclusion criteria were hypothyroidism, diabetes mellitus, alcohol addictive patients, peptic ulcer, any gastrointestinal upset, renal impairment, and any hepatic or cardiac problem. All patients were divided in three groups (group-A, group-B, group-C), 25 in each group. Their baseline experimental data was taken and filed in specifically designed Performa, at start of taking medicine, like lipid profile, blood pressure and pulse rate. The study period was eight weeks. Twenty five patients of group-A were advised to take one tea spoon of Nigella sativa (Kalonji), twice daily, i.e.; one tea spoon after breakfast and one tea spoon after dinner. Twenty-five patients of group-B were advised to take Gemfibrozil 600 mg tablets, one after breakfast and one after dinner. Twenty-five patients were provided placebo capsules, (containing grinded wheat), taking one capsule after breakfast and another before going to bed. All participants were advised to take these medicines for eight weeks. They were also advised for 20 minutes brisk walk at morning or evening time. Patients were called every 2 weeks for follow up to check blood pressure, weight, pulse rate and general appearance of the individual. Drug compliance to the regimen was monitored by interview and counseling at each clinical visits. Serum LDL-cholesterol was calculated by Friedwald formula (LDL-Cholesterol = Total Cholesterol-(Triglycerides/5 +HDL-Cholesterol). Data were expressed as the mean ± SD and “t” test was applied to determine statistical significance as the difference. A probability value of ‹0.05 was considered as non-significancant and P‹0.001 was considered as highly significant.

Results

When results were compiled and statistically analyzed, it was observed that Nigella sativa and Gemfibrozil decreased LDLcholesterol significantly. Nigella sativa decreased LDL cholesterol from 191.14±3.45 mg/dl to 159.40±2.98 mg/dl. This change in mean values was 31.7 mg/dl with highly significant p-value of ‹0.001 (Table 1). Gemfibrozil decreased LDL cholesterol from 197.77±3.91 mg/dl to 159.62±2.20 mg/dl. In mean values this change was 38.2 mg/dl with highly significant p-value of ‹0.001 (Table 2). Placebo group showed LDL cholesterol reduction from 163.10±1.45 mg/dl to 159.40±1.77 mg/dl. This change in mean values was 3.7 mg/dl, with non-significant p-value of >0.05 (Table 3).