Literature DB >> 15280100

Expression of cytochrome P450-4A isoforms in the rat cremaster muscle microcirculation.

Jingli Wang1, Kristopher G Maier, Richard J Roman, Lourdes De La Cruz, Jiaxuan Zhu, Lisa Henderson, Julian H Lombard.   

Abstract

OBJECTIVE: This study sought to identify any specific cytochrome P450 (CYP450) -4A enzyme isoforms expressed in arterioles and/or the surrounding parenchymal tissue of the rat cremaster muscle.
METHODS: RT-PCR was used to detect the presence of specific CYP450-4A isoforms in isolated muscle fibers and arterioles from the cremaster muscle of Sprague-Dawley rats; CYP450-4A protein expression was determined by Western blotting.
RESULTS: CYP450-4A3 mRNA was expressed in isolated muscle fibers and in cremasteric arterioles, while CYP450-4A8 mRNA was expressed only in cremasteric arterioles. CYP450-4A1 and CYP450-4A2 mRNA were not expressed in arterioles and skeletal muscle cells, although all four isoforms were strongly expressed in the liver. CYP450-4A protein was detected in both the isolated muscle fibers and in the isolated arterioles.
CONCLUSIONS: The present study identifies the specific pattern of cytochrome P450-4A isoform expression in arterioles and parenchymal cells of the skeletal muscle microcirculation, and supports the hypothesis that the cytochrome P-450 enzymes may play a role in the regulation of microvascular function in the skeletal muscle microcirculation.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15280100     DOI: 10.1080/10739680490266225

Source DB:  PubMed          Journal:  Microcirculation        ISSN: 1073-9688            Impact factor:   2.628


  7 in total

1.  Modulation by cytochrome P450-4A ω-hydroxylase enzymes of adrenergic vasoconstriction and response to reduced PO₂ in mesenteric resistance arteries of Dahl salt-sensitive rats.

Authors:  Gábor Raffai; Jingli Wang; Richard J Roman; Siddam Anjaiah; Brian Weinberg; John R Falck; Julian H Lombard
Journal:  Microcirculation       Date:  2010-10       Impact factor: 2.628

Review 2.  Role of the CYP4A/20-HETE pathway in vascular dysfunction of the Dahl salt-sensitive rat.

Authors:  Kathleen M Lukaszewicz; Julian H Lombard
Journal:  Clin Sci (Lond)       Date:  2013-06       Impact factor: 6.124

3.  Reduced angiotensin II levels cause generalized vascular dysfunction via oxidant stress in hamster cheek pouch arterioles.

Authors:  Jessica R C Priestley; Matthew W Buelow; Scott T McEwen; Brian D Weinberg; Melanie Delaney; Sarah F Balus; Carlyn Hoeppner; Lynn Dondlinger; Julian H Lombard
Journal:  Microvasc Res       Date:  2013-04-27       Impact factor: 3.514

4.  Introgression of Brown Norway CYP4A genes on to the Dahl salt-sensitive background restores vascular function in SS-5(BN) consomic rats.

Authors:  Kathleen M Lukaszewicz; John R Falck; Vijaya L Manthati; Julian H Lombard
Journal:  Clin Sci (Lond)       Date:  2013-03       Impact factor: 6.124

5.  Role of vascular reactive oxygen species in regulating cytochrome P450-4A enzyme expression in Dahl salt-sensitive rats.

Authors:  Kathleen M Lukaszewicz; Mahesh P Paudyal; John R Falck; Julian H Lombard
Journal:  Microcirculation       Date:  2016-10       Impact factor: 2.628

6.  Expression of CYP 4A ω-hydroxylase and formation of 20-hydroxyeicosatetreanoic acid (20-HETE) in cultured rat brain astrocytes.

Authors:  Debebe Gebremedhin; David X Zhang; Koryn A Carver; Nicole Rau; Kevin R Rarick; Richard J Roman; David R Harder
Journal:  Prostaglandins Other Lipid Mediat       Date:  2016-05-09       Impact factor: 3.072

7.  Modulation of vascular O2 responses by cytochrome 450-4A omega-hydroxylase metabolites in Dahl salt-sensitive rats.

Authors:  Jingli Wang; James R Schmidt; Richard J Roman; Siddam Anjaiah; John R Falck; Julian H Lombard
Journal:  Microcirculation       Date:  2009-02-16       Impact factor: 2.628

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.