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一种修饰的胰岛素B21-26片段(β-丙氨酸-精氨酸-甘氨酸-苯丙氨酸-苯丙氨酸-酪氨酸-氨基)的胰岛素样活性和胰岛素增强作用。

Insulin-like activities and insulin-potentiating actions of a modified insulin B21-26 fragment: beta-Ala-Arg-Gly-Phe-Phe-Tyr-NH2.

作者信息

Fujino M, Wakimasu M, Taketomi S, Iwatsuka H

出版信息

Endocrinology. 1977 Aug;101(2):360-4. doi: 10.1210/endo-101-2-360.

Abstract

A modified sequence of insulin B21-26, beta-Ala-Arg-Gly-Phe-Phe-Tyr-NH2 (DP-432), was synthesized and tested for its biological activities. The hexapeptide, ip injected to mice, stimulated [U-14C]-glucose incorporation into diaphragm glycogen and adipose tissue total lipid. Neither plasma glucose nor FFA (free fatty acid) was reduced by the injection. However, when injected with epinephrine, the peptide prevented a rise of plasma FFA but not that of plasma glucose due to epinephrine. In vitro, the peptide stimulated glucose oxidation and inhibited epinephrine- or isoproterenol-stimulated lipolysis of mouse adipose tissue. Furthermore, when added along with insulin to incubation media, the peptide exaggerated the effects of insulin on both glucose oxidation and isoproterenol-stimulated lipolysis. The hexapeptide thus seems to have an insulin-potentiating action as well as insulin like activities on peripheral tissue.

摘要

合成了胰岛素B21 - 26的修饰序列β - 丙氨酸 - 精氨酸 - 甘氨酸 - 苯丙氨酸 - 苯丙氨酸 - 酪氨酸 - 氨基(DP - 432),并对其生物活性进行了测试。将该六肽腹腔注射到小鼠体内,可刺激[U - 14C] - 葡萄糖掺入膈肌糖原和脂肪组织总脂质中。注射后血浆葡萄糖和游离脂肪酸(FFA)均未降低。然而,当与肾上腺素一起注射时,该肽可阻止因肾上腺素引起的血浆FFA升高,但不能阻止血浆葡萄糖升高。在体外,该肽可刺激葡萄糖氧化,并抑制肾上腺素或异丙肾上腺素刺激的小鼠脂肪组织脂解。此外,当与胰岛素一起添加到孵育培养基中时,该肽可增强胰岛素对葡萄糖氧化和异丙肾上腺素刺激的脂解的作用。因此,该六肽似乎具有胰岛素增强作用以及对外周组织的类胰岛素活性。

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