期刊文献+

酚妥拉明对离体正常大鼠胰岛功能的影响 被引量:1

Effects of Phentolamine on the Function of Isolated Islets of Normal Rats
原文传递
导出
摘要 目的 探讨酚妥拉明对离体正常大鼠胰岛功能的影响。方法 胶原酶和DNA酶联合消化法分离SD大鼠胰岛 ,RP MI164 0组织培养液过夜培养 ,采用MilliporeMultiscreen系统观察不同浓度葡萄糖及酚妥拉明对胰岛功能的影响。放免法测定孵育液中胰岛素及胰高糖素的浓度。结果 ⑴离体胰岛胰岛素的分泌依赖于孵育液中的葡萄糖浓度 ,酚妥拉明明显刺激其释放。Ca2 +通道阻滞剂硝苯吡啶 (2 5 μmol/L)及K+ 通道开放剂二氮嗪 (10 0 μmol/L)可显著抑制胰岛素的释放 ,但其作用可被酚妥拉明消除。⑵离体胰岛胰高糖素的分泌明显受葡萄糖浓度的抑制 ,酚妥拉明显著抑制其分泌 ,其抑制作用呈明显的浓度依赖型 ,硝苯吡啶和二氮嗪也显著抑制胰高糖素的释放。结论 酚妥拉明可刺激离体胰岛胰岛素的释放 ,抑制胰高糖素的分泌 。 Objective To explore the effects of phentolamine on the function of the islets isolated from normal rats.Methods The SD rats islets were isolated by digestive method with collagenase and DNase.Millipore Multiscreen Assay System was used to observe the effects of phentolamine on the function of isolated islets. Insulin and glucagon were measured by RIA. Results ⑴Insulin secretion of the isolated islets incubated in culture medium was glucose concentration-dependent manner. Phentolamine had stimulate insulin secretion significantly. Nifedipine (Ca 2+ channel blocker) and diazoxide (K + channel opener) had inhibit the insulin release, but their effects were abolished by phentolamine. ⑵Glucagon secretion of the isolated islets in culture medium incubated was inhibited by glucose. Phentolamine inhibited glucagon secretion significantly, and the inhibiting effect was also concentration-dependent manner,both the nifedipine and diazoxide had the effect too. Conclusion Phentolamine could stimulate insulin secretion, and inhibit glucagon secretion in the isolated islets.It maybe has some hypoglycemic effects on diabetes.
出处 《中国医师杂志》 CAS 2003年第1期40-42,共3页 Journal of Chinese Physician
关键词 酚妥拉明 离体胰岛 胰岛素 胰高糖素 动物实验 Phentolamine Isolated islets Insulin Glucagon Rats
  • 相关文献

参考文献1

  • 1K. Bokvist,H.L. Olsen,M. H?y,C.F. Gotfredsen,W.F. Holmes,K. Buschard,P. Rorsman,J. Gromada. Characterisation of sulphonylurea and ATP-regulated K+ channels in rat pancreatic A-cells[J] 1999,Pflügers Archiv(4):428~436

同被引文献10

  • 1Efendic S, Efanov AM, Berggren PO, et al. Two generations of insulinotropic imidazoline compounds[J]. Diabetes, 2002,51:S448-5411
  • 2Lefebvre PJ. Glucagon and its family, revisted[J]. Diabetes care,1995,18:715-730
  • 3Rustenbeck I, Kopp M, Ratzka P, et al. Imidazolines and the pancreatic B-cell actions and binding sites[J]. Ann N Y Acad Sci, 1999,881:229-240
  • 4Molderings GJ. Imidazoline receptor: basic knowledge, recent advances and future prospects for therapy and diagnosis[J]. Drugs Fut, 1997,22:757-772
  • 5Zaitsev SV, Efanov AE, Efanov IB, et al. Imidazoline compounds stimulate insulin release by inhibition of KATP channels and interaction with the exocytotic machinery[J]. Diabetes, 1996,45:1610-1618
  • 6Panten U, Schwanstecher M, Schwanstecher C. Sulfonylurea receptors and mechanism of sulfonlurea action. Exp. Clin. Endocrinol[J]. Diabetes,1996,104:1-9
  • 7Papaccio G, Nicoletti F, Pisanti FA, et al. An imidazoline compound completely counteracts interleukin-1[beta] toxic effects to rat pancreatic islet [beta] cells[J]. Mol Med,2002,8:536-545
  • 8Velliquette RA, Ernsberger P. The role of I(1)-imidazoline and alpha(2)-adrenergic receptors in the modulation of glucose metabolism in the spontaneously hypertensive obese rat model of metabolic syndrome X[J]. J Pharmacol Exp Ther,2003,306:646-657
  • 9Hφy M, Bokvist K, Weng XG, et al. Phentolamine inhibits exocytosis of glucagon by Gi2 protein-dependent activation of calcineurin in rat pancreatic α-cells[J]. J Boil Chem, 2001,276:925-930
  • 10Bokvist K, Olsen HL, Hφy M, et al. Characterization of sulfonlurea and ATP-regulated K+ channels in rat pancreatic A-cells[J]. Eur J Physiol,1999, 438(7):428-436

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部