Literature DB >> 10945853

Influence of heme oxygenase inhibitors on the basal tissue enzymatic activity and smooth muscle relaxation of internal anal sphincter.

S Rattan1, S Chakder.   

Abstract

We examined the actions of different heme oxygenase (HO) inhibitors on the basal HO activity in the opossum internal anal sphincter (IAS), rectum, and liver tissues and the IAS smooth muscle relaxation in response to nonadrenergic noncholinergic (NANC) nerve stimulation and different agonists. All the tissues examined were found to have significant levels of basal HO activity. Among different HO inhibitors, tin protoporphyrin IX (SnPP IX) was found to be most selective in inhibiting the HO activity in the IAS smooth muscle. Conversely, in the liver, all the HO inhibitors except SnPP IX caused significant inhibition of HO activity. Consistent with HO activity inhibition, the IAS smooth muscle relaxations caused by NANC nerve stimulation and vasoactive intestinal polypeptide also were inhibited by zinc protoporphyrin IX and SnPP IX. Zinc protoporphyrin IX also caused a significant attenuation of the IAS smooth muscle relaxation caused by isoproterenol. The IAS smooth muscle relaxation caused by nitric oxide was not significantly modified by any of the HO inhibitors. The data show the presence of HO activity in the IAS and other gastrointestinal tissues. The differential attenuation of HO activity by different HO inhibitors in the IAS smooth muscle and liver confirms the presence of different isozymes of HO in different tissues. Suppression of basal HO activity and the IAS smooth muscle relaxation induced by NANC nerve stimulation or VIP but not NO suggest that some of the stimuli that cause IAS smooth muscle relaxation may involve HO activity.

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Year:  2000        PMID: 10945853

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  5 in total

1.  Heme-oxygenase-2 immunolabelling in pig jejunum.

Authors:  Nilce Mitiko Matsuda; Steven M Miller; Joseph H Szurszewski
Journal:  Acta Histochem       Date:  2009-02-20       Impact factor: 2.479

2.  Cobalt Protoporphyrin Upregulates Cyclooxygenase-2 Expression Through a Heme Oxygenase-Independent Mechanism.

Authors:  Hsiao-Yun Lin; Chon-Haw Tsai; Chingju Lin; Wei-Lan Yeh; Cheng-Fang Tsai; Pei-Chun Chang; Ling-Hsuan Wu; Dah-Yuu Lu
Journal:  Mol Neurobiol       Date:  2015-08-09       Impact factor: 5.590

3.  Carbon monoxide mediates vasoactive intestinal polypeptide-associated nonadrenergic/noncholinergic neurotransmission.

Authors:  Crystal C Watkins; Darren Boehning; Adam I Kaplin; Mahil Rao; Christopher D Ferris; Solomon H Snyder
Journal:  Proc Natl Acad Sci U S A       Date:  2004-02-24       Impact factor: 11.205

4.  Zinc Protoporphyrin Suppresses β-Catenin Protein Expression in Human Cancer Cells: The Potential Involvement of Lysosome-Mediated Degradation.

Authors:  Shuai Wang; Bethany N Hannafon; Stuart E Lind; Wei-Qun Ding
Journal:  PLoS One       Date:  2015-05-22       Impact factor: 3.240

5.  Blocking heme oxygenase-1 by zinc protoporphyrin reduces tumor hypoxia-mediated VEGF release and inhibits tumor angiogenesis as a potential therapeutic agent against colorectal cancer.

Authors:  Chun-Chia Cheng; Siao-Syun Guan; Hao-Jhih Yang; Chun-Chao Chang; Tsai-Yueh Luo; Jungshan Chang; Ai-Sheng Ho
Journal:  J Biomed Sci       Date:  2016-01-28       Impact factor: 8.410

  5 in total

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