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长效生长抑素类似物奥曲肽对胰腺摄取血浆氨基酸的影响。

Effect of octreotide, a long-acting somatostatin analogue, on plasma amino acid uptake by the pancreas.

作者信息

Gullo L, Pezzilli R, Ancona D, Labate A M, Barbara L

机构信息

Unit for the Study of Pancreatic Diseases, University of Bologna, Sant'Orsola Hospital, Italy.

出版信息

Pancreas. 1991 Nov;6(6):668-72. doi: 10.1097/00006676-199111000-00008.

Abstract

Octreotide (SMS 201-995) is a long-acting somatostatin analogue that inhibits exocrine pancreatic secretion and that has been proposed for treatment of various pancreatic disorders. To gain more information about the mechanism by which octreotide inhibits pancreatic enzyme secretion, we studied the effect of this compound on plasma amino acid uptake by the pancreas in six healthy volunteers aged 22-29 years. Pancreatic amino acid uptake was assessed by measuring plasma amino acid concentration before and during pancreatic enzyme synthesis stimulation with cerulein (50 ng/kg/h). The infusion of cerulein caused a significant decrease (p less than 0.001) in plasma amino acid concentration. The subcutaneous injection of octreotide at dosages of 12.5, 25, and 50 micrograms prevented this decrease in a dose-dependent manner. The decrease in amino acid concentration reached a maximum of 19.4 +/- 2.4% during cerulein infusion and a maximum of 10.7 +/- 2.5, 6.8 +/- 1.2, and 2.9 +/- 1.2% (means +/- SD) when cerulein was preceded by injection of octreotide at 12.5, 25, and 50 mg, respectively. These results indicate that octreotide is able to inhibit the plasma amino acid uptake by pancreatic acinar cells and, consequently, synthesis of pancreatic enzymes. Clinically, this effect could be useful in treatment of pathologic conditions of the pancreas in which it is desirable to suppress acinar cell activity and avoid accumulation of enzymes in acinar cells.

摘要

奥曲肽(SMS 201-995)是一种长效生长抑素类似物,可抑制胰腺外分泌,已被用于治疗各种胰腺疾病。为了获取更多关于奥曲肽抑制胰腺酶分泌机制的信息,我们研究了该化合物对6名年龄在22 - 29岁健康志愿者胰腺摄取血浆氨基酸的影响。通过测量用雨蛙素(50 ng/kg/h)刺激胰腺酶合成之前及期间的血浆氨基酸浓度来评估胰腺对氨基酸的摄取。输注雨蛙素导致血浆氨基酸浓度显著降低(p < 0.001)。皮下注射12.5、25和50微克剂量的奥曲肽可呈剂量依赖性地阻止这种降低。在雨蛙素输注期间,氨基酸浓度降低最多达19.4±2.4%,而在分别注射12.5、25和50微克奥曲肽后再输注雨蛙素时,氨基酸浓度降低最多分别为10.7±2.5%、6.8±1.2%和2.9±1.2%(均值±标准差)。这些结果表明,奥曲肽能够抑制胰腺腺泡细胞摄取血浆氨基酸,从而抑制胰腺酶的合成。临床上,这种作用可能有助于治疗需要抑制腺泡细胞活性并避免酶在腺泡细胞中蓄积的胰腺病理状况。

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