Fontaine J, Reuse J
Arch Int Pharmacodyn Ther. 1978 Sep;235(1):51-61.
The effects of metoclopramide (Mcp), sulpiride (Sp) and some of their derivatives: bromopride (Br), tiapride (Ti) and sultopride (Stp) have been compared on the guinea-pig isolated ileum. 1. Br and Ti have, like Mcp, and indirect cholinergic stimulating effect on the intestinal smooth muscle. Sp and Stp are devoid of such an effect. 2. At high doses, all the benzamides have a direct inhibitory effect on the ileum. 3. Mcp, Br and Ti (10(-5)M) potentiate the responses of the ileum to acetylcholine (ACh). At high doses (10(-4)M) the effects of all benzamides on the responses to ACh as well as to histamine (H) are mostly inhibitory. 4. Mcp and Br (10(-5)M) inhibit the responses of the ileum to serotonin (5HT) while Ti, Sp and Stp potentiate them. 5. Neural pathways and calcium mechanisms are involved in the potentiations of ACh and 5HT responses since the enhancements observed are abolished in the presence of tetrodotoxin or in the absence of Ca++.
已在豚鼠离体回肠上比较了胃复安(Mcp)、舒必利(Sp)及其一些衍生物:溴必利(Br)、硫必利(Ti)和舒托必利(Stp)的作用。1. Br和Ti与Mcp一样,对肠道平滑肌有间接胆碱能刺激作用。Sp和Stp没有这种作用。2. 在高剂量时,所有苯甲酰胺类药物对回肠都有直接抑制作用。3. Mcp、Br和Ti(10⁻⁵M)增强回肠对乙酰胆碱(ACh)的反应。在高剂量(10⁻⁴M)时,所有苯甲酰胺类药物对ACh以及组胺(H)反应的影响大多是抑制性的。4. Mcp和Br(10⁻⁵M)抑制回肠对5-羟色胺(5HT)的反应,而Ti、Sp和Stp则增强这些反应。5. 由于在存在河豚毒素或无Ca²⁺的情况下观察到的增强作用被消除,因此神经通路和钙机制参与了ACh和5HT反应的增强。