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大鼠附睾白色脂肪组织与肩胛间棕色脂肪组织对脂肪动力物质反应性的差异。

Differences in responsiveness to adipokinetic agents between white epididymal and brown interscapula adipose tissue from rats.

作者信息

Itaya K

出版信息

J Pharm Pharmacol. 1978 Oct;30(10):632-7. doi: 10.1111/j.2042-7158.1978.tb13345.x.

Abstract

Lipolytic activity was studied in brown and white adipose tissue of rats in vitro. 5-Hydroxy-tryptamine (5-HT), phenylephrine, noradrenaline, adrenaline and isoprenaline were used as adipokinetic agents. All stimulated lipolysis in brown adipose tissue, but 5-HT and phenyl-ephrine did not in white adipose tissue. A beta-blocking drug, propranolol, inhibited the stimulatory effect of the agents in both adipose tissues. However, an alpha-blocking drug, phentolamine, further increased the lipolysis induced by noradrenaline or adrenaline in brown adipose tissue and inhibited the effect of isoprenaline. In white adipose tissue, its action was to marginally decrease the effect of adrenaline and noradrenaline. Increase in the pH of the incubation medium stimulated FFA and glycerol release in brown adipose tissue, but not in the epididymal adipose tissue. This effect of pH on lipolysis was further enhanced by phentolamine and decreased by propranolol. Increase of lipolysis with pH was not seen with brown fat tissue from the reserpine-treated rats. These results show that brown adipose tissue of the rat has an alpha-receptor with inhibitory effects on lipolysis that is affected by alpha- or mixed-type adrenergic agonists, noradrenaline and adrenaline.

摘要

在体外对大鼠的棕色和白色脂肪组织中的脂解活性进行了研究。使用5-羟色胺(5-HT)、去氧肾上腺素、去甲肾上腺素、肾上腺素和异丙肾上腺素作为脂肪动力学剂。所有这些物质均刺激棕色脂肪组织中的脂解作用,但5-HT和去氧肾上腺素对白色脂肪组织无此作用。一种β受体阻断药物普萘洛尔抑制了这两种脂肪组织中这些药剂的刺激作用。然而,一种α受体阻断药物酚妥拉明进一步增强了去甲肾上腺素或肾上腺素在棕色脂肪组织中诱导的脂解作用,并抑制了异丙肾上腺素的作用。在白色脂肪组织中,其作用是略微降低肾上腺素和去甲肾上腺素的作用。孵育培养基pH值的升高刺激了棕色脂肪组织中游离脂肪酸(FFA)和甘油的释放,但对附睾脂肪组织无此作用。酚妥拉明进一步增强了pH值对脂解的这种作用,而普萘洛尔则使其减弱。利血平处理的大鼠的棕色脂肪组织未出现随着pH值升高脂解增加的情况。这些结果表明,大鼠的棕色脂肪组织具有一种对脂解有抑制作用的α受体,该受体受α型或混合型肾上腺素能激动剂去甲肾上腺素和肾上腺素的影响。

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