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首页> 外文期刊>Journal of medicinal food >Effect of kaikasaponin III obtained from Pueraria thunbergiana flowers on serum and hepatic lipid peroxides and tissue factor activity in the streptozotocin-induced diabetic rat.
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Effect of kaikasaponin III obtained from Pueraria thunbergiana flowers on serum and hepatic lipid peroxides and tissue factor activity in the streptozotocin-induced diabetic rat.

机译:从葛根花获得的kaikasaponin III对链脲佐菌素诱导的糖尿病大鼠血清和肝脂质过氧化物及组织因子活性的影响。

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摘要

We investigated the effect of kaikasaponin III (KS-III) on Phase I and II enzymes and tissue factor (TF) activity to elucidate the pharmacological actions of this immunosuppressive saponin in the diabetic rat. This compound was obtained from the flower of Pueraria thunbergiana (Leguminosae) by chromatographic isolation. This crude drug (Puerariae Flos) has been used as a therapeutic agent for diabetes mellitus in traditional Korean medicine. KS-III prolonged the bleeding time and plasma clotting time in streptozotocin (STZ)-treated rats and increased the TF activity, suggesting that this compound has anti-thrombosis activity in STZ-induced rats. It also inhibited the formation of malondialdehyde (MDA) and hydroxy radicals in serum and liver, but promoted superoxide dismutase (SOD) activity. Low MDA concentrations and low xanthine oxidase and aldehyde oxidase activities were observed in the KS-III-treated rats, suggesting that such Phase I enzyme activities are the major source of lipid peroxidation. However, KS-III increased Phase II enzyme activities such as SOD, glutathione peroxidase, and catalase, suggesting the activation of free radical-scavenging enzymes. These results suggest that KS-III may exhibit its hypoglycemic and hypolipidemic effects by up-regulating or down-regulating antioxidant mechanisms via the changes in Phase I and II enzyme activities.
机译:我们调查了kaikasaponin III(KS-III)对I和II期酶和组织因子(TF)活性的影响,以阐明这种免疫抑制性皂苷在糖尿病大鼠中的药理作用。该化合物通过色谱分离从葛根(Leerminosae)的花中获得。在韩国传统医学中,这种粗制药物(Puerariae Flos)已被用作糖尿病的治疗剂。 KS-III延长了链脲佐菌素(STZ)处理的大鼠的出血时间和血浆凝结时间,并增加了TF活性,表明该化合物在STZ诱导的大鼠中具有抗血栓形成活性。它还抑制血清和肝脏中丙二醛(MDA)和羟基自由基的形成,但促进超氧化物歧化酶(SOD)活性。在KS-III处理的大鼠中观察到低的MDA浓度以及低的黄嘌呤氧化酶和醛氧化酶活性,表明这种I期酶活性是脂质过氧化的主要来源。但是,KS-III增加了II期酶的活性,例如SOD,谷胱甘肽过氧化物酶和过氧化氢酶,表明自由基清除酶的活化。这些结果表明,KS-III可能通过上调或下调抗氧化机制(通过I和II期酶活性的变化)表现出降血糖和降血脂作用。

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