Methoxy flavonoid compound as medicament for preventing and controlling metabolism complex disease and using method
A technology for methoxyflavonoids and metabolic syndrome, applied in the field of methoxyflavonoids, can solve the problems of low yield, high price, inability to carry out experimental research, etc., to reduce the incidence of complications, prolong the survival period, Reduce the effect of the cardiovascular system
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Embodiment 1
[0033] Sixty male mice were randomly divided into 4 groups, 15 in each group and 5 in each cage. Food and water were given ad libitum, and feed and water consumption was calculated daily. Both the solvent and the drug were intragastrically administered at 10ml / kg body weight once a day. A: normal feed + solvent, B: normal feed + PMQ (50mg / kg / d), C: high-fat feed + solvent, D: high-fat feed + PMQ (50mg / kg / d). lasts for 3 months. The animals were fasted for 12 hours before slaughter, anesthetized with ether, and blood was collected from the orbit to prepare serum. Slaughter animals, carry out relevant parameter measurement, the result is as follows:
[0034] 1. Whether it is normal feed or high-fat feed, there is no significant difference in feed consumption and drinking water between PMQ group and solvent control group. Prompt that the drug does not affect appetite.
[0035] 2. Whether it is normal feed or high-fat feed, the body weight of PMQ group is significantly lower ...
Embodiment 2
[0039]Male SD rats, weighing about 250g, were prepared with 2 kidneys and 1 clip as a model of renal hypertension. After the operation, high-fat diets were fed. After the blood pressure increased significantly, the islet β cells were damaged with alloxan, and the blood sugar increased. . Finally, a metabolic syndrome model (expressed as elevated blood pressure, high blood triglycerides, high blood total cholesterol, and high blood sugar) was formed. One week after islet injury, the animals were divided into a treatment group (PMQ 50 mg / kg / d) and a solvent control group, and administered by intragastric administration. Before administration and every 10 days or longer after administration, blood was collected from the orbit under light ether anesthesia to prepare serum. The result is as follows:
[0040] 1. After modeling, the food intake and water intake of the solvent control group were higher than those of the PMQ group, but their body weight no longer increased or decreas...
Embodiment 3
[0046] Male SD rats, weighing about 250 g, took the thoracic aorta after anesthesia, and prepared arterial ring specimens with a width of about 0.3-0.4 cm. The changes in vascular tension were measured in the isolated organ bath under conditions close to the internal environment. The results are as follows:
[0047] 1. PQM can concentration-dependently resist the degree of vasoconstriction caused by methoxyamine;
[0048] 2. In the vascular specimens pre-contracted with methoxyamine, PQM produced a concentration-dependent relaxation effect. In the specimens without endothelium, the relaxation effect was significantly weakened, but not disappeared. It shows that its vasodilation effect has two components involved in the vascular endothelium-dependent and vascular endothelium-independent components.
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