Key result
Gelidium amansii extract cuts hepatic cholesterol ~16% in diabetic rats without improving glucose intolerance.
Why the study?
The effects of Gelidium amansii hot-water extracts on lipid and glucose metabolism in streptozotocin/nicotinamide-induced diabetic rats were unclear.
Does Gelidium amansii hot-water extract alleviate abnormal lipid and glucose metabolism in a diabetic rat model?
Does Gelidium amansii hot-water extract alleviate abnormal lipid and glucose metabolism in a diabetic rat model?
Absolute Event Rate: 81.2% vs 96.3%
p-value: p=<0.05
Gelidium amansii hot-water extracts improve hepatic lipid metabolism but not glucose intolerance in a diabetic rat model.
) hot-water extracts (GHE) on lipid and glucose metabolism in rats with streptozotocin (STZ)/nicotinamide (NA)-induced diabetes. Rats were divided into three groups: NC-normal control group), DM-diabetic group, and DG-diabetic group supplemented with GHE (5%). The experimental diet and drinking water were available ad libitum for 10 weeks. After the 10-week feeding duration, the body weight, liver weight, total adipose tissue weight, and hepatic TBARS and cholesterol levels were significantly increased, and hepatic glycogen content and adipose lipolysis rate were significantly decreased in the DM group, which could be effectively reversed by supplementation of GHE. However, GHE supplementation could not improve the glucose intolerance in DM rats. It was interesting to note that GHE supplementation could decrease the liver glucose-6-phosphotase activity, which was increased in DM rats. Taken together, these results suggested that GHE feeding may ameliorate abnormal hepatic lipid metabolism, but not glucose intolerance, in diabetic rats induced by STZ/NA.
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Liu et al. (2022) studied Streptozotocin/nicotinamide-induced diabetes (n=21). Gelidium amansii hot-water extract (GHE) vs. High-fat diet without GHE was evaluated on Hepatic Total Cholesterol (mg/g liver) (p=<0.05). Supplementation with 5% Gelidium amansii hot-water extract significantly reduced hepatic total cholesterol and ameliorated abnormal hepatic lipid metabolism in diabetic rats, without improving glucose intolerance.
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