Vasoactive intestinal polypeptide inhibits pacemaker activity via the nitric oxide-cGMP-protein kinase G pathway in the interstitial cells of Cajal of the murine small intestine.

@article{Kim2006, abstract = {Interstitial cells of Cajal (ICCs) are pacemaker cells that activate the periodic spontaneous depolarization (pacemaker potentials) responsible for the production of slow waves in gastrointestinal smooth muscle. The effects of vasoactive intestinal polypeptide (VIP) on the pacemaker potentials in cultured ICCs from murine small intestine were investigated by whole-cell patch-clamp techniques. Addition of VIP (50 nM-1 microM) decreased the amplitude of pacemaker potentials and depolarized resting membrane potentials. To examine the type of receptors involved in ICC, we examined the effects of the VIP1 agonist and found that it had no effect on pacemaker potentials. Pretreatment with VIP1 antagonist (1 microM) for 10 min also did not block the VIP (50 nM)-induced effects. On the other hand exposure to 1H-(1,2,4)oxadiazolo(4,3-A)quinoxalin- 1-one (ODQ, 100 microM), an inhibitor of guanylate cyclase, prevented VIP inhibition of pacemaker potentials. Similarly KT-5823 (1 microM) or RP-8-CPT-cGMPS (10 microM), inhibitors of protein kinase G (PKG) blocked the effect of VIP (50 nM) on pacemaker potentials as did N-nitro-L-arginine (L-NA, 100 mM), a non-selective nitric oxide synthase (NOS) inhibitor. These results imply that the inhibition of pacemaker activity by VIP depends on the NO-cGMP-PKG pathway.}, author = {Kim, Byung J. and Lee, Jae H. and Jun, Jae Y. and Chang, In Y. and So, Insuk and Kim, Ki W. }, citeulike-article-id = {2053692}, journal = {Mol Cells}, keywords = {agents, animal, article-pka-pkg, balb, biological, cell, clock, cultured, cyclic, electrophysiology, enzyme, female, gmp, gmp-dependent, inbred, inhibitor, intestinal, intestine, kinase, male, mice, nitric, oxide, patch-clamp, peptide, protein, signal, small, techniques, transduction, vasoactive, vasodilator}, month = {Jun}, number = {3}, pages = {337--342}, posted-at = {2007-12-04 01:53:37}, priority = {2}, title = {Vasoactive intestinal polypeptide inhibits pacemaker activity via the nitric oxide-c{GMP}-protein kinase {G} pathway in the interstitial cells of {C}ajal of the murine small intestine.}, volume = {21}, year = {2006} }

TY - JOUR ID - Kim2006 L3 - citeulike-article-id:2053692 TI - Vasoactive intestinal polypeptide inhibits pacemaker activity via the nitric oxide-c{GMP}-protein kinase {G} pathway in the interstitial cells of {C}ajal of the murine small intestine. JF - Mol Cells VL - 21 IS - 3 SP - 337 EP - 342 N2 - Interstitial cells of Cajal (ICCs) are pacemaker cells that activate the periodic spontaneous depolarization (pacemaker potentials) responsible for the production of slow waves in gastrointestinal smooth muscle. The effects of vasoactive intestinal polypeptide (VIP) on the pacemaker potentials in cultured ICCs from murine small intestine were investigated by whole-cell patch-clamp techniques. Addition of VIP (50 nM-1 microM) decreased the amplitude of pacemaker potentials and depolarized resting membrane potentials. To examine the type of receptors involved in ICC, we examined the effects of the VIP1 agonist and found that it had no effect on pacemaker potentials. Pretreatment with VIP1 antagonist (1 microM) for 10 min also did not block the VIP (50 nM)-induced effects. On the other hand exposure to 1H-(1,2,4)oxadiazolo(4,3-A)quinoxalin- 1-one (ODQ, 100 microM), an inhibitor of guanylate cyclase, prevented VIP inhibition of pacemaker potentials. Similarly KT-5823 (1 microM) or RP-8-CPT-cGMPS (10 microM), inhibitors of protein kinase G (PKG) blocked the effect of VIP (50 nM) on pacemaker potentials as did N-nitro-L-arginine (L-NA, 100 mM), a non-selective nitric oxide synthase (NOS) inhibitor. These results imply that the inhibition of pacemaker activity by VIP depends on the NO-cGMP-PKG pathway. KW - agents KW - animal KW - article-pka-pkg KW - balb KW - biological KW - cell KW - clock KW - cultured KW - cyclic KW - electrophysiology KW - enzyme KW - female KW - gmp KW - gmp-dependent KW - inbred KW - inhibitor KW - intestinal KW - intestine KW - kinase KW - male KW - mice KW - nitric KW - oxide KW - patch-clamp KW - peptide KW - protein KW - signal KW - small KW - techniques KW - transduction KW - vasoactive KW - vasodilator AU - Kim, Byung AU - Lee, Jae AU - Jun, Jae AU - Chang, In AU - So, Insuk AU - Kim, Ki PY - 2006/Jun// ER -