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大鼠下丘脑提取物可在体外增强胰岛素分泌。

A rat hypothalamic extract enhances insulin secretion in vitro.

作者信息

Bobbioni E, Jeanrenaud B

出版信息

Endocrinology. 1983 Dec;113(6):1958-62. doi: 10.1210/endo-113-6-1958.

DOI:10.1210/endo-113-6-1958
PMID:6357763
Abstract

Fractions from a partially purified ventrolateral hypothalamic (VLH) extract stimulate insulin (IRI) secretion when infused into isolated perfused rat pancreases. At a low glucose concentration (5 mM) in the perfusion medium, infusion of the VLH extract significantly increased insulin output when compared to controls infused with a cerebellar cortex extract. (IRI output with cerebellar cortex: 13.5 +/- 0.81; with VLH extracts: 40.9 +/- 9.4 ng/5 min, P less than 0.05). At a high glucose concentration (10 mM) in the perfusion medium, IRI secretion evoked by glucose was further augmented by the simultaneous infusion of the VLH extract (IRI output with glucose: 325.6 +/- 25.8; glucose + VLH extract: 448.1 +/- 33.0 ng/20 min, P less than 0.02). When pancreases were perfused with a solution containing 20 different amino acids [(AA) 6.6 mM final concentration] IRI secretion elicited by the AA was similarly augmented by the presence of the VLH extract (IRI output with AA: 101.8 +/- 14.9; AA + VLH extract: 179.8 +/- 21.9, P less than 0.02). However, IRI secretion as stimulated by arginine alone (3 mM) was not potentiated by the extract. It is suggested that the hypothalamic factor(s) responsible for this IRI secretion-promoting activity could contribute to the hypothalamic control of IRI secretion through a route which remains to be established.

摘要

将部分纯化的下丘脑腹外侧核(VLH)提取物注入离体灌注的大鼠胰腺时,其组分可刺激胰岛素(IRI)分泌。在灌注液中葡萄糖浓度较低(5 mM)时,与注入小脑皮质提取物的对照组相比,注入VLH提取物可显著增加胰岛素分泌量。(注入小脑皮质提取物后的IRI分泌量:13.5±0.81;注入VLH提取物后的IRI分泌量:40.9±9.4 ng/5分钟,P<0.05)。在灌注液中葡萄糖浓度较高(10 mM)时,同时注入VLH提取物可使葡萄糖诱导的IRI分泌进一步增加(葡萄糖刺激后的IRI分泌量:325.6±25.8;葡萄糖+VLH提取物:448.1±33.0 ng/20分钟,P<0.02)。当用含有20种不同氨基酸(终浓度6.6 mM)的溶液灌注胰腺时,VLH提取物的存在同样可增加氨基酸诱导的IRI分泌(氨基酸刺激后的IRI分泌量:101.8±14.9;氨基酸+VLH提取物:179.8±21.9,P<0.02)。然而,提取物不能增强单独由精氨酸(3 mM)刺激引起的IRI分泌。提示负责这种促进IRI分泌活性的下丘脑因子可能通过一条尚待确定的途径参与下丘脑对IRI分泌的调控。

相似文献

1
A rat hypothalamic extract enhances insulin secretion in vitro.大鼠下丘脑提取物可在体外增强胰岛素分泌。
Endocrinology. 1983 Dec;113(6):1958-62. doi: 10.1210/endo-113-6-1958.
2
Effect of rat hypothalamic extract administration on insulin secretion in vivo.
Endocrinology. 1982 Feb;110(2):631-6. doi: 10.1210/endo-110-2-631.
3
Interaction of gastric inhibitory polypeptide, glucose, and arginine on insulin and glucagon secretion from the perfused rat pancreas.胃抑制性多肽、葡萄糖和精氨酸对灌注大鼠胰腺胰岛素和胰高血糖素分泌的相互作用。
Endocrinology. 1978 Aug;103(2):610-5. doi: 10.1210/endo-103-2-610.
4
Characterization of the effects of arginine and glucose on glucagon and insulin release from the perfused rat pancreas.精氨酸和葡萄糖对灌注大鼠胰腺胰高血糖素和胰岛素释放影响的表征
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Reversible impairment of glucose-induced insulin secretion in SHR/N-cp rats. Genetic model of type II diabetes.SHR/N-cp大鼠中葡萄糖诱导的胰岛素分泌的可逆性损伤。II型糖尿病的遗传模型。
Diabetes. 1988 Apr;37(4):398-404. doi: 10.2337/diab.37.4.398.
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Glucagon release induced by ventrolateral hypothalamic stimulation in the rat.大鼠下丘脑腹外侧刺激诱导的胰高血糖素释放
Endocrinology. 1980 May;106(5):1612-9. doi: 10.1210/endo-106-5-1612.
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Insulin content and insulinogenesis by the perfused rat pancreas: effects of long term glucose stimulation.灌注大鼠胰腺的胰岛素含量及胰岛素生成:长期葡萄糖刺激的影响
Endocrinology. 1986 Jan;118(1):170-5. doi: 10.1210/endo-118-1-170.
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Consequences of ventromedial hypothalamic lesions upon insulin and glucagon secretion by subsequently isolated perfused pancreases in the rat.大鼠下丘脑腹内侧核损伤对随后分离的灌注胰腺胰岛素和胰高血糖素分泌的影响。
J Clin Invest. 1980 Apr;65(4):902-10. doi: 10.1172/JCI109744.
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Neuroendocrine control of insulin secretion.胰岛素分泌的神经内分泌控制。
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10
[In vitro and in vivo effect of gold thioglucose on the insulin- and glucagon-secretion of the isolated perfused rat pancreas].[硫代葡萄糖金对离体灌注大鼠胰腺胰岛素和胰高血糖素分泌的体外和体内作用]
Biomed Biochim Acta. 1986;45(4):507-22.

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Endocrine. 1995 Jan;3(1):55-9. doi: 10.1007/BF02917449.
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An hypothesis on the aetiology of obesity: dysfunction of the central nervous system as a primary cause.关于肥胖病因的一种假说:中枢神经系统功能障碍是主要原因。
Diabetologia. 1985 Aug;28(8):502-13. doi: 10.1007/BF00281984.