Literature DB >> 10500074

Monochloramine directly modulates Ca(2+)-activated K(+) channels in rabbit colonic muscularis mucosae.

M Prasad1, J B Matthews, X D He, H I Akbarali.   

Abstract

BACKGROUND & AIMS: Mesenteric ischemia, infection, and inflammatory bowel disease may eventuate in severe colitis, complicated by toxic megacolon with impending intestinal perforation. Monochloramine (NH(2)Cl) is a membrane-permeant oxidant generated during colitis by the large amount of ambient luminal NH(3) in the colon. Reactive oxygen metabolites can modulate smooth muscle ion channels and thereby affect colonic motility, which is markedly impaired in colitis.
METHODS: Effects of NH(2)Cl on ionic currents in the innermost smooth muscle layer of the colon, the tunica muscularis mucosae, were examined using the patch clamp technique. Membrane potential in whole tissue strips was measured using high-resistance microelectrodes.
RESULTS: Whole cell voltage clamp experiments showed that NH(2)Cl (3-30 micromol/L) enhanced outward currents in a dose-dependent manner, increasing currents more than 8-fold at a test potential of +30 mV. Tail current analysis showed that the currents enhanced by NH(2)Cl were K(+) currents. Inhibition by tetraethylammonium and iberiotoxin suggested that these currents represented activation of large-conductance, Ca(2+)-activated K(+) channels. The membrane-impermeant oxidant taurine monochloramine, however, had no effect on whole cell currents. Single-channel studies in inside-out patches showed that NH(2)Cl increased open probability of a 257-pS channel in symmetrical (140 mmol/L) K(+). In the presence of NH(2)Cl, the steady-state voltage dependence of activation was shifted by -22 mV to the left with no change in the single-channel amplitude. The sulfhydryl alkylating agent N-ethylmaleimide prevented NH(2)Cl-induced channel activation. NH(2)Cl also hyperpolarized intact muscle strips, an effect blocked by iberiotoxin.
CONCLUSIONS: NH(2)Cl, at concentrations expected to be found during colitis, may contribute to smooth muscle dysfunction by a direct oxidant effect on maxi K(+) channels.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10500074     DOI: 10.1016/s0016-5085(99)70350-1

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  7 in total

Review 1.  Ion channel remodeling in gastrointestinal inflammation.

Authors:  H I Akbarali; E G Hawkins; G R Ross; M Kang
Journal:  Neurogastroenterol Motil       Date:  2010-07-05       Impact factor: 3.598

2.  Stimulation of colonic anion secretion by monochloramine: action sites.

Authors:  Gerhard Schultheiss; Sarah Lán Kocks; Martin Diener
Journal:  Pflugers Arch       Date:  2004-12-23       Impact factor: 3.657

3.  Capsaicin induces NKCC1 internalization and inhibits chloride secretion in colonic epithelial cells independently of TRPV1.

Authors:  Patrice G Bouyer; Xu Tang; Christopher R Weber; Le Shen; Jerrold R Turner; Jeffrey B Matthews
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2012-11-08       Impact factor: 4.052

4.  ZnT2-Mediated Zinc Import Into Paneth Cell Granules Is Necessary for Coordinated Secretion and Paneth Cell Function in Mice.

Authors:  Abigail B Podany; Justin Wright; Regina Lamendella; David I Soybel; Shannon L Kelleher
Journal:  Cell Mol Gastroenterol Hepatol       Date:  2016-01-08

5.  The physiology and pharmacology of singlet oxygen.

Authors:  Thomas W Stief
Journal:  Med Hypotheses       Date:  2003-04       Impact factor: 1.538

Review 6.  Postranslational Modification of Ion Channels in Colonic Inflammation.

Authors:  Hamid I Akbarali; Minho Kang
Journal:  Curr Neuropharmacol       Date:  2015       Impact factor: 7.363

7.  Nitric oxide decreases the excitability of interstitial cells of Cajal through activation of the BK channel.

Authors:  Yaohui Zhu; Jan D Huizinga
Journal:  J Cell Mol Med       Date:  2008-01-11       Impact factor: 5.310

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.