Key result
Serotonin stimulates guanylyl cyclase to increase cGMP formation, suggesting a novel 5-HTGC receptor subtype.
Why the study?
The mechanisms by which serotonin activates guanylyl cyclase, potentially through a novel serotonin receptor subtype, were not fully characterized.
Answers are grounded in this paper and cite their sources.
In vitro cGMP findings in NG108-15 cells should not change practice; leaves open additive ANP-serotonin interactions for further study.
Characterization of the serotonin-induced increase in guanosine 3',5'-cyclic monophosphate (cyclic GMP) was investigated and compared with that induced by atrial natriuretic peptide (ANP) in NG108-15 cells. The cyclic GMP formed by serotonin or ANP was transported in a similar manner to the extracellular medium, although the cyclic GMP formed by bradykinin was not. Serotonin and ANP raised cyclic GMP additively. Serotonin-induced cyclic GMP formation was completely inhibited by pretreatment with 100 nM 12-o-tetradecanoylphorbol 13-acetate (TPA), although that induced by ANP was only partially inhibited and the effects were blocked by pretreatment with staurosporin. In membrane preparations, ANP stimulated cyclic GMP formation in the presence of ATP, but serotonin did not. Serotonin-stimulated cyclic GMP formation was found to occur in neuroblastoma N18TG-2, but not in glioma C6Bu-1. These results suggest that a novel subtype of serotonin receptors (5-HTGC) which stimulates membrane-bound guanylyl cyclase, different from that stimulated by natriuretic peptide, may exist especially in neurons.
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Tohda et al. (1995) studied this question. Serotonin vs. Atrial natriuretic peptide (ANP) was evaluated on Cyclic GMP formation. Serotonin stimulated membrane-bound guanylyl cyclase to increase cyclic GMP formation in neuronal cell lines, suggesting the existence of a novel serotonin receptor subtype (5-HTGC).
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