首页> 外文期刊>Biological & pharmaceutical bulletin >Anti-obesity and anti-diabetic activities of a new beta3 adrenergic receptor agonist, (S)-(Z)-[4-[[1-[2-[(2-hydroxy-3-phenoxypropyl)]amino]ethyl]-1-prop enyl] phenoxy] acetic acid ethanedioic acid (SWR-0342SA), in KK-Ay mice.
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Anti-obesity and anti-diabetic activities of a new beta3 adrenergic receptor agonist, (S)-(Z)-[4-[[1-[2-[(2-hydroxy-3-phenoxypropyl)]amino]ethyl]-1-prop enyl] phenoxy] acetic acid ethanedioic acid (SWR-0342SA), in KK-Ay mice.

机译:一种新型的β3肾上腺素能受体激动剂(S)-(Z)-[4-[[1- [2-[(2-羟基-3-苯氧基丙基)]氨基]乙基]-的抗肥胖和抗糖尿病活性KK-Ay小鼠体内的1-丙烯基]苯氧基]乙酸乙二酸(SWR-0342SA)。

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摘要

We investigated the beta-adrenergic receptor (AR) agonistic activities in rats and humans, and the anti-obesity and anti-diabetic activities in KK-Ay mice, of a new beta3-AR agonist, SWR-0342SA ((S)-(Z)-[4-[[1-[2-[(2-hydroxy-3-phenoxypropyl)]amino]ethyl]-1-pro penyl]phenoxy] acetic acid ethanedioic acid). With regards to its beta-AR agonistic activity in rats, SWR-0342SA stimulated the atrial beating rate (beta1-AR activity) and white adipocyte lipolysis (beta3-AR activity), but did not induce uterine muscle relaxation (beta2-AR activity). The beta3-AR agonistic activity of SWR-0342SA was about 20 times stronger than its beta1-AR agonistic activity. Similarly, SWR-0342SA enhanced the accumulation of cAMP in Chinese hamster ovary (CHO) cells expressing human beta1- and beta3-ARs, while having no effect in CHO cells expressing beta2-ARs. Adenylyl cyclase stimulation by SWR-0342SA in CHO cells expressing beta3-ARs was about 35 times higher than that in CHO cells expressing beta1-ARs. With regards to anti-obesity and anti-diabetic activities, SWR-0342SA had no effect on body weight or food intake, but slightly decreased the fat pads weight in KK-Ay mice, an animal model of obesity and non-insulin-dependent diabetes mellitus (NIDDM). On the other hand, SWR-0342SA significantly decreased both blood glucose (to about 46% of control) and serum insulin levels (to about 40% of control) in KK-Ay mice. These results indicated that SWR-0342SA is a selective beta3-AR agonist, and possesses potent anti-diabetic activity, and that the anti-obesity activity is inferior to the anti-diabetic activity.
机译:我们研究了一种新的β3-AR激动剂SWR-0342SA((S)-()对大鼠和人类的β-肾上腺素受体(AR)激动活性以及KK-Ay小鼠的抗肥胖和抗糖尿病活性。 Z)-[4-[[[1- [2-[(2-羟基-3-苯氧基丙基)氨基]乙基] -1-丙基]苯氧基]乙酸乙二酸)。关于它在大鼠中的β-AR激动活性,SWR-0342SA刺激了心房跳动率(β1-AR活性)和白色脂肪细胞脂解(β3-AR活性),但没有引起子宫肌松弛(β2-AR活性)。 。 SWR-0342SA的beta3-AR激动活性比其beta1-AR激动活性强约20倍。同样,SWR-0342SA增强了cAMP在表达人beta1-和beta3-ARs的中国仓鼠卵巢(CHO)细胞中的积累,而在表达beta2-ARs的CHO细胞中没有作用。 SWR-0342SA在表达beta3-ARs的CHO细胞中对腺苷酸环化酶的刺激作用比表达beta1-ARs的CHO细胞高35倍。关于抗肥胖和抗糖尿病活性,SWR-0342SA对体重或食物摄入量没有影响,但略微降低了肥胖和非胰岛素依赖型糖尿病动物模型KK-Ay小鼠的脂肪垫重量(NIDDM)。另一方面,SWR-0342SA可显着降低KK-Ay小鼠的血糖(至对照组的46%)和血清胰岛素水平(至对照组的40%)。这些结果表明SWR-0342SA是选择性的β3-AR激动剂,并且具有有效的抗糖尿病活性,并且抗肥胖活性不如抗糖尿病活性。

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