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1.
Bahrain Medical Bulletin. 2011; 33 (1): 32-36
in English | IMEMR | ID: emr-131026

ABSTRACT

The habit of khat chewing represents a major socio-economic problem in many countries but research into its hepato-renal toxic effects has produced contradictory results. To evaluate the subacute effects of Khat [Catha edulis] extract on hepatic and renal functions in white albino rats. Randomized experimental animal study. Physiology laboratory, medical school of King Khalid University. Twenty white albino rats aged between 14 and 16 weeks were included in the study. The rats were assigned randomly into two groups, ten each. Treated rats received orally administered hydro-ethanol extract of Catha edulis for four weeks. Control rats received corresponding amounts of normal saline. There was statistically significant increase in the activities of hepatic enzymes in treated rats compared to the control group. In addition, serum urea, bilirubin and phosphorus concentrations were significantly increased compared to a decreased serum total protein and albumin concentrations. Oral administration of the extract induced lipid peroxidation and oxidative stress in hepatic and renal tissues as shown by significant increases in lipid peroxidation biomarkers thiobarbituric acid reactive substances [TBARS] and significant decreases in levels of superoxide dismutase [SOD], catalase [CAT] and glutathione [GSH]. Histological examination of Catha edulis treated rats revealed marked hepato-renal pathological changes compared to the control group. These results indicate that orally administered Catha edulis extract exerts severe hepato-nephro toxicity and the mechanism of this damage may be related to oxidation, increased lipid peroxidation, and generation of free radicals inside these tissues

2.
Saudi Journal of Gastroenterology [The]. 2009; 15 (2): 104-110
in English | IMEMR | ID: emr-92566

ABSTRACT

Amiodarone, a class III antiarrhythmic drug, has been found to be effective in the management of patients with life-threatening ventricular arrhythmias. The aim of this study was to test whether the co administration of vitamin-E with amiodarone can reduce amiodarone-induced liver damage. Twelve male albino rats were divided into three groups [ml vegetable oil/day by oral gavages daily for 2 weeks and were used as control group. The rats of the second group received 5.4 mg amiodarone/100 gm rat dissolved in vegetable oil daily by oral gavages for 2 weeks. In the third group, the rats received 5.4 mg amiodarone and 5 mg vitamin-E/100 gram rat dissolved in 2 ml vegetable oil by oral gavages daily for 2 weeks. Two weeks after treatment, the rats were sacrificed and liver specimens were immediately taken and processed for transmission electron microscopic examinations. Sections from the rat liver receiving amiodarone examined by electron microscopy showed disrupted hepatocytes with increased vacuolations. Degenerated organelles and disrupted nuclei were observed. The microvilli of bile canaliculi were disrupted and the hepatocytes showed increased lipid contents. Both endothelial cells and Kupffer cells were damaged. Phospholipids inside the mitochondria showed a loss of cristae. Sections from the liver of rats received amiodarone and vitamin-E showed lesser effects, especially in depositions of phospholipids in the mitochondria and the whole organelles and the nucleus showed minor damage in comparison to the previous group. Milder hepatotoxic effects are seen in rats administered amiodarone and vitamin E simultaneously suggesting that vitamin-E may play a role in amelioration of the effects of amiodarone


Subject(s)
Animals, Laboratory , Amiodarone/adverse effects , Amiodarone , Amiodarone/pharmacokinetics , Arrhythmias, Cardiac , Tocopherols/pharmacokinetics , Chemical and Drug Induced Liver Injury/etiology , Hepatocytes/ultrastructure , Rats , Liver/drug effects
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