Copyright
©The Author(s) 2016.
World J Gastrointest Pathophysiol. Feb 15, 2016; 7(1): 150-159
Published online Feb 15, 2016. doi: 10.4291/wjgp.v7.i1.150
Published online Feb 15, 2016. doi: 10.4291/wjgp.v7.i1.150
Figure 5 Bradykinin-evoked increase in short-circuit current is mainly mediated by the prostaglandin E2 receptors.
A: Pretreatment with EP receptors antagonist AH6809, SC-19220 (a selective antagonist of EP1 receptor), or GW627368X (a selective antagonist of EP4 receptor) suppressed BK-evoked Isc (P < 0.01); B: Quantitative data showing the effect of AH6809, Sc-19220 and GW627368X on BK-evoked response in Isc. The vertical axis represents the changes of Isc. Values are expressed as mean ± SE, n = 6-12 animals. eP < 0.01 (compared to BK alone). BK: Bradykinin; PGE2: Prostaglandin E2; Isc: Increase in short-circuit current.
- Citation: Qu MH, Ji WS, Zhao TK, Fang CY, Mao SM, Gao ZQ. Neurophysiological mechanisms of bradykinin-evoked mucosal chloride secretion in guinea pig small intestine. World J Gastrointest Pathophysiol 2016; 7(1): 150-159
- URL: https://www.wjgnet.com/2150-5330/full/v7/i1/150.htm
- DOI: https://dx.doi.org/10.4291/wjgp.v7.i1.150