- Author:
Huan XUE
1
;
Xiang-Qin ZHONG
1
;
Meng-Meng LIU
1
;
Zhi-Hong LU
1
;
Zhi-Tong WEN
1
;
Li-Juan CUI
1
;
Xiao-Yuan SHI
1
;
Hao-Jie XING
1
;
Xin ZHAO
1
;
Yu-Shan ZHANG
1
;
Yi ZHANG
1
Author Information
- Publication Type:Journal Article
- Keywords: action potential duration; D2-like receptors; dopamine; insulin secretion; voltage-dependent potassium channels; whole-cell patch-clamp
- From: Chinese Pharmacological Bulletin 2022;38(1):105-109
- CountryChina
- Language:Chinese
- Abstract: Aim To study the electrophysiological mechanism of dopamine inhibiting insulin secretion hv voltage-dependent potassium ( Kv) channels.Methods Islets and (3 cells were isolated from male SD rats.D,-like receptor agonist ( SKP38393), D2-like receptor agonist (Quinpirole) and antagonist (Epiclopride) were used according to the experiment.Insulin secretion was detected by insulin radioimmunoassay.Whole-cell j J patch-clamp technique was applied to detect Kv channel currents and action potential duration of p cells.Di- BAC4(3) staining was used to observe membrane potential.Results SKF38393 did not affect insulin secretion and the Kv channel currents.Quinpirole signifi cantly inhibited insulin secretion and increased Kv channel currents.Dopamine significantly inhibited insulin secretion, increased Kv channel currents and shortened action potential duration of p cells, which could be reversed by epiclopride.In addition, dopamine de-creased membrane potential of INS-1 cells.Conclusions Dopamine inhibits insulin secretion by acting on D2-like receptors, resulting in actived Kv channels, shortened action potential duration and decreased cell membrane potential.