Bodziony J, Schwille P O
Department of Surgery, University of Erlangen, FRG.
Exp Clin Endocrinol. 1989;94(3):338-44. doi: 10.1055/s-0029-1210919.
The release of insulin, glucagon and somatostatin from islets isolated by microdissection, and islets isolated by aid of different duration of collagenase digestion from pancreases with exocrine atrophy was assessed. Prior collagenase digestion caused an increased release of insulin and glucagon, but not somatostatin; also, the non-suppressibility of glucagon secretion despite high glucose concentration in the medium was characteristic for those islets. Additional data suggest that in the absence of intrinsic pancreatic proteases the nature of the damage conferred by collagenase to islet B- and A-cells is different. In the light of action of epinephrine, an inhibitor of insulin secretion, possible mechanisms responsible for disturbed hormone release in the presence of proteolytic enzymes are discussed.
评估了通过显微解剖分离的胰岛以及从外分泌萎缩的胰腺经不同时长胶原酶消化辅助分离的胰岛中胰岛素、胰高血糖素和生长抑素的释放情况。预先进行胶原酶消化会导致胰岛素和胰高血糖素释放增加,但生长抑素释放未增加;此外,对于那些胰岛而言,尽管培养基中葡萄糖浓度很高,胰高血糖素分泌仍不可抑制是其特征。其他数据表明,在缺乏胰腺内源性蛋白酶的情况下,胶原酶对胰岛B细胞和A细胞造成损伤的性质有所不同。鉴于肾上腺素(一种胰岛素分泌抑制剂)的作用,讨论了在存在蛋白水解酶时激素释放紊乱的可能机制。