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25. Holzer, U., F.K. Krapfenbauer, and W.H. Dwoskin. 2011. Activation of 5-HT4 receptors inhibits CCK receptor-mediated chloride secretion in the guinea pig distal ascending colon. Am. J. Physiol. Gastrointest. Liver Physiol. 300:G116-122.
In the same study, the 5-HT4 antagonist RS39604 was shown to suppress the effect of CCK-8, as expected. In addition, the group showed that selective 5-HT4 receptors also mediate CCK1 receptor mediated contractions in the guinea pig distal ascending colon.
The same group showed in a similar study that CCK2 receptor mediated contractions are also under the control of 5-HT4 receptors. This time, the 5-HT4 receptor agonist SB222200 was used to activate 5-HT4 receptors. The K(+) currents through mucosal 5-HT4, CCKA, CCKB, and CCK2 receptors were found to be enhanced in the presence of tetrodotoxin via an NO/cGMP pathway. This indicates an osmotic stimulus, possibly acting through aqueous humor production. This is a bit trivial as the authors also claimed the aqueous humor production of the guinea pig is not significantly different from human.
The authors also commented on the lack of effect of mosapride (5-HT4 agonist) on K(+) currents unless the osmolarity of the bath solution is high. They concluded that the effect of mosapride on K(+) currents is influenced by the osmolarity of the bathing solution. Anyway, this consequence of their findings may have implications for other studies conducted using mosapride and the potential differences of osmolarity of the bath solutions required to see an effect if mosapride activates 5-HT4 receptors. See discussion of above. d2c66b5586
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