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Mechanism of the salutary effects of flutamide on intestinal myeloperoxidase activity following trauma‐hemorrhage: up‐regulation of estrogen receptor‐β‐dependent HO‐1
Author(s) -
Yu HuangPing,
Choudhry Mashkoor A.,
Shimizu Tomoharu,
Hsieh YaChing,
Schwacha Martin G.,
Yang Shaolong,
Chaudry Irshad H.
Publication year - 2006
Publication title -
journal of leukocyte biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.819
H-Index - 191
eISSN - 1938-3673
pISSN - 0741-5400
DOI - 10.1189/jlb.0705363
Subject(s) - biology , mechanism (biology) , myeloperoxidase , estrogen , estrogen receptor , medicine , endocrinology , pharmacology , immunology , inflammation , cancer , breast cancer , philosophy , genetics , epistemology
Hemeoxygenase (HO)‐1 induction following adverse circulatory conditions is known to be protective, and precastrated males have less intestinal damage than sham‐operated males following trauma‐hemorrhage (T‐H). Previous studies have also shown that administration of flutamide up‐regulated estrogen receptor (ER) expression in males following T‐H. We hypothesized that flutamide administration in males following T‐H up‐regulates HO‐1 via an ER‐dependent pathway and protects against intestinal injury. Male Sprague‐Dawley rats underwent T‐H [mean blood pressure (MBP) 40 mmHg for 90 min and then resuscitation]. A single dose of flutamide (25 mg/kg body weight), with or without an ER antagonist (ICI 182,780), a HO enzyme inhibitor [chromium‐mesoporphyrin (CrMP)], or vehicle, was administered subcutaneously during resuscitation. At 2 h after T‐H or sham operation, intestinal myeloperoxidase (MPO) activity, intercellular adhesion molecule (ICAM)‐1, cytokine‐induced neutrophil chemoattractant (CINC)‐1, and CINC‐3 levels were measured. Intestinal ER‐α, ER‐β, androgen receptor, and HO‐1 mRNA/protein levels were also determined. Results showed that T‐H increased intestinal MPO activity, ICAM‐1, CINC‐1, and CINC‐3 levels. These parameters were improved significantly in the flutamide‐treated rats subjected to T‐H. Flutamide treatment increased intestinal HO‐1 and ER‐β mRNA/protein levels as compared with vehicle‐treated T‐H rats. Administration of the ER antagonist ICI 182,780 or the HO inhibitor CrMP prevented the flutamide‐induced attenuation of shock‐induced intestinal damage. Thus, the salutary effects of flutamide administration on attenuation of intestinal injury following T‐H are mediated via up‐regulation of ER‐β‐dependent HO‐1 expression.