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Ischemic preconditioning mediated by activation of KATP channels in rat small intestine

  
@article{APS7632,
	author = {Shuang-ping Yang and Yi-bin Hao and Yu-xiu Wu and Wen Dun and Li-hong Shen and Yi Zhang},
	title = {Ischemic preconditioning mediated by activation of KATP channels in rat small intestine},
	journal = {Acta Pharmacologica Sinica},
	volume = {20},
	number = {4},
	year = {2016},
	keywords = {},
	abstract = {AIM:
To study whether the protective effects of ischemic preconditioning against rat small intestine ischemia/reperfusion injury could be mediated by KATP channel opener.
METHODS:
Preconditioning (Pc) was induced by 3 cycles of 8-min superior mesenteric artery (SMA) occlusion and 10-min reperfusion before prolonged ischemia. Cromakalim (Cro 75 micrograms.kg-1) and glibenclamide (Gli 8 mg.kg-1) were injected i.v. 10 min before prolonged ischemia and Pc, respectively.
RESULTS:
Compared with ischemic reperfusion (IR) group, Pc before prolonged ischemia (Pc + IR) decreased LDH release [(380 +/- 55) vs (559 +/- 49) U.L-1, P < 0.05], attenuated intestinal edema [wet weight/dry weight (WW/DW), 5.6 +/- 0.6 vs 6.34 +/- 0.29, P < 0.05], ameliorated intestinal histological damage (grading scale, 3.4 vs 5.7, P < 0.01), and improved reperfusion-induced hypotension. These effects of Pc were mimicked by Cro [LDH, (298 +/- 40) vs (559 +/- 49) U.L-1, P < 0.05; WW/DW, 5.6 +/- 0.4 vs 6.34 +/- 0.29, P < 0.05; grading scale, 3.6 vs 5.7, P < 0.01] and abolished in the presence of Gli [LDH, (624 +/- 44) vs (559 +/- 49) U.L-1; WW/DW, 6.6 +/- 0.6 vs 6.34 +/- 0.29; grading scale, 5.7 vs 5.7; P > 0.05] compared with IR group, respectively.
CONCLUSION:
Ischemic preconditioning on the rat small intestine is mediated by activation of KATP channels.},
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/7632}
}