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1.
J Biosci ; 2006 Dec; 31(5): 575-9
Article in English | IMSEAR | ID: sea-111016

ABSTRACT

Diabetes mellitus (DM)is a multi-factorial disease which is characterized by hyperglycaemia, lipoprotein abnormalities and oxidative stress. This study evaluated effect of oral vitamin C administration on basal metabolic rate and lipid profile of alloxan-induced diabetic rats. Vitamin C was administered at 200 mg/kg body wt. by gavage for four weeks to diabetic rats after which the resting metabolic rate and plasma lipid profile was determined. The results showed that vitamin C administration significantly (p less than 0.01) reduced the resting metabolic rate in diabetic rats; and also lowered plasma triglyceride, total cholesterol and low-density lipoprotein cholesterol. These results suggest that the administration of vitamin C in this model of established diabetes mellitus might be beneficial for the restoration of basal metabolic rate and improvement of lipid profile. This may at least in part reduce the risk of cardiovascular events seen in diabetes mellitus.


Subject(s)
Animals , Ascorbic Acid/therapeutic use , Basal Metabolism/drug effects , Diabetes Mellitus, Experimental/drug therapy , Lipid Metabolism/drug effects , Male , Rats , Rats, Wistar
2.
Article in English | AIM | ID: biblio-1267761

ABSTRACT

The effect of an aqueous leaf of Ageratum conyzoides on gastric acid secretion in rats was investigated in 18 albino rats of Wistar strain. The rats were divided into 2 groups of 9 each. Gastric acid output was determined by continuous perfusion in urethane anaesthetized rats. Control gastric acid output was obtained usign 0.9


Subject(s)
Ageratum , Gastric Acid , Rats
3.
Niger. j. physiol. sci ; 19(1): 1-6, 2004.
Article in English | AIM | ID: biblio-1267483

ABSTRACT

The haematological effects following ingestion of shellfish exposed to crude oil polluted water or the pollutant perse were investigated in albino Wistar rats. Feeding of four groups of rats for 28 days duration with two reference casein or shellfish protein control diets (Group A and B); and two test diets (Group C and D) supplemented at varying levels with shellfish which had been previously exposed to crude oil polluted water and the oral gavaging with crude oil at the rate of 3; 6 and 9 ml/kg body weight per day to three groups (groups II; III and IV respectively) of rats for 7 days duration resulted in changes in packed cell volume (PCV); red blood cell (RBC) and white blood cell (WBC) counts; and haemoglobin concentration (Hb) of rats. Group C and D respectively fed 10 and 20 polluted shellfish diets recorded significant (P 0.05) decreases in PCV and RBC counts while Hb concentration and WBC counts increased. Groups II; III and IV gavaged with varying doses of crude oil recorded significant (P 0.05 - 0.01) dose dependent decrease in PCV and RBC counts when compared to controls (group 1). Hb and WBC counts also increased for these groups but the increase was only significant for WBC counts (P 0.05) when compared with controls. The results suggest that the ingestion of shellfish exposed to crude oil polluted water or the polluted perse results in haematotoxicity


Subject(s)
Petroleum , Shellfish
4.
Indian J Physiol Pharmacol ; 1993 Jul; 37(3): 199-203
Article in English | IMSEAR | ID: sea-106434

ABSTRACT

Sodium-potassium ATPase activity and transmembrane calcium influx in the aortic smooth muscle from control and diabetic rats were assessed indirectly through the measurement of KCl relaxation and contractile responses to CaCl2 in attempts to explain the contractile responses to KCl following streptozotocin-induced diabetes mellitus. There were no significant changes in the maximum contractile responses of the aortas from 4 and 12 week diabetic rats to KCl even when significant increases in calcium influx were demonstratable. On the other hand, the diabetic aortas were significantly (P < 0.05) more sensitive to KCl-induced relaxations than the controls. This provides an indirect evidence for increased activity of the sodium-postassium ATPase enzyme in the aortas from streptozotocin diabetic rats. This may, atleast in part, explain the inability of KCl to produce greater than normal contractions of the aortas from diabetic rats.


Subject(s)
Animals , Aorta/drug effects , Calcium/metabolism , Calcium Chloride/pharmacology , Diabetes Mellitus, Experimental/physiopathology , Male , Muscle Contraction/drug effects , Muscle Relaxation/drug effects , Muscle, Smooth, Vascular/drug effects , Potassium Chloride/pharmacology , Rats , Rats, Wistar , Sodium-Potassium-Exchanging ATPase/metabolism
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