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The Effect And Signaling Mechanism Of UrotensinⅡ On Cardiac Function

Posted on:2009-07-24Degree:MasterType:Thesis
Country:ChinaCandidate:C J LiFull Text:PDF
GTID:2144360245468921Subject:Department of Cardiology
Abstract/Summary:PDF Full Text Request
AIM To investigate the effect and signaling mechanism of urotensin II on cardiac function in normal and heart failure rats.Methods Hearts were perfused in the Langendorff mode,⑴UII group: Urotensin II (10-10,10-9,10-8 and 10-7 mol﹒L-1) was given respectively perfusion , then investigated the normal and heart failure rat's cardiac function;⑵KT5720+UII group : perfused UII( IC50 ) on the basis of KT5720 , observed normal and heart failure rat's cardiac function ;⑶KT5720 group : recorded normal and heart failure rat's hemodynamic index after perfused KT5720.Results⑴UII group: After given UII (10-10,10-9,10-8 and 10-7 mol﹒L-1) in the fluid ,①normal rats : +dp/dtmax decreased 16.48%,25.53%,31.53% and 34.47%, -dp/dtmax reduced 22.78%,33.63%,46.09% and 51.73%;②heart failure rats : +dp/dtmax decreased 19.01%,26.05%,34.36%,37.27%, -dp/dtmax reduced 27.71%,38.72%,53.41%,60.12%, respectively. The heart failure rats'ratio was higher than normal rats'.⑵KT5720+UII group : urotensin II( IC50 ) was given on the basis of KT5720 ,①normal rats : +dp/dtmax reduced 5.37%, -dp/dtmax decreased 7.59%;②heart failure rats : +dp/dtmax reduced 3.27%, -dp/dtmax decreased 3.15%. There were significantly differences between KT5700+UII and UII group in±dp/dtmax(normal rat and heart failure rat: P<0.01)⑶KT5720 group : after perfused KT5720 ,①normal rats: +dp/dtmax decreased 5.99%, -dp/dtmax decreased 7.63%;②heart failure rats : +dp/dtmax decreased 2.84%, -dp/dtmax decreased 2.96%. In normal and heart failure rats , there were no significantly differences between KT5720+UII group and KT5720 group in±dp/dtmax, (P>0.05) .Conclusions The inhibitory effect of UII on normal and heart failure rat's cardiac function was dose dependent , KT5720 could inhibit this effect, so the mechanism of UII on normal and heart failure rat's cardiac function was probably mediated by PKA.
Keywords/Search Tags:Urotensin II, KT5720, isolated heart, cardiac function, mechanism
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