Cholecystokinin-induced contraction of dispersed smooth muscle cells

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Abstract
Isolated smooth muscle cells were prepared from the fundus of guinea pig stomach by incubation with collagenase. Incubating the cells with the C-terminal octapeptide of cholecystokinin [CCK] induced contraction, which was measured by micrometry and expressed as percent decrease in mean cell length. CCK-induced contraction was maximal within 30 s and reduced cell length by .apprx. 37%. The threshold concentration of CCK was 0.1 pM, and the maximally effective concentration was 0.3 nM. Contraction caused by CCK was inhibited by proglumide and by glucagon. Inhibition by proglumide was competitive and resulted in a parallel rightward shift of the CCK dose-response curve. Inhibition by glucagon was noncompetitive and resulted in a reduction in the efficacy of CCK without a change in its potency. Proglumide-induced inhibition was specific for CCK; glucagon-induced inhibition of contraction was nonspecific and reduced the contraction caused by carbamylcholine and the calcium ionophore A23187 [calcimycin].