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WAY-202196, a selective estrogen receptor-beta agonist, protects against death in experimental septic shock.
- Source :
-
Critical care medicine [Crit Care Med] 2006 Aug; Vol. 34 (8), pp. 2188-93. - Publication Year :
- 2006
-
Abstract
- Objective: To determine the effect of an estrogen receptor-beta selective agent in experimental models of systemic infection and sepsis.<br />Design: WAY-202196, a nonsteroidal selective estrogen receptor-beta agonist, was tested in the murine listeriosis model, the neutropenic rat Pseudomonas aeruginosa infection, and the mouse cecal ligation and puncture sepsis models.<br />Setting: University-affiliated biomedical research laboratory.<br />Subjects: BALB/c mice and Sprague-Dawley rats.<br />Interventions: WAY-202196 or control (vehicle) was administered orally in doses ranging from 1.5 to 50 mg/kg at various time points in the three experimental model systems.<br />Measurements and Main Results: Susceptibility of mice treated with a single oral dose of up to 50 mg/kg WAY-202196 did not differ from those treated with vehicle alone after systemic challenge by Listeria monocytogenes, suggesting a lack of generalized immunosuppression. In the neutropenic rat model, daily administration of WAY-202196 (50 mg/kg) significantly increased survival against an otherwise lethal challenge of P. aeruginosa 12.4.4 compared with the control group (83% vs. 25% survival; p < 0.05). Preservation of intestinal mucosal weight and prevention of histopathologic changes were also observed with the administration of WAY-202196. Similar results were obtained in a cecal ligation and puncture model, in which multiple oral doses of WAY-202196 (50 mg/kg) improved survival (83% vs. 0%; p < 0.05), preserved intestinal epithelial integrity, and significantly reduced systemic bacteremia and peritoneal interleukin-6 and tumor necrosis factor levels. The estrogen receptor-beta agonist provided a comparable level of protection in both male and female animals.<br />Conclusion: These results indicate that oral administration of WAY-202196 preserved gastrointestinal barrier function and improved outcome in experimental models of systemic infection and inflammation. WAY-202196 and similar agents may prove useful clinically as a novel treatment strategy for the treatment or prevention of severe sepsis.
- Subjects :
- Administration, Oral
Animals
Ascitic Fluid metabolism
Bacteremia drug therapy
Bacteremia microbiology
Disease Models, Animal
Estrogen Receptor beta agonists
Female
Interleukin-6 metabolism
Intestinal Mucosa drug effects
Intestinal Mucosa ultrastructure
Listeria monocytogenes
Male
Mice
Mice, Inbred BALB C
Neutropenia complications
Pseudomonas Infections drug therapy
Rats
Rats, Sprague-Dawley
Shock, Septic microbiology
Tumor Necrosis Factor-alpha metabolism
Naphthols pharmacology
Shock, Septic drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 0090-3493
- Volume :
- 34
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- Critical care medicine
- Publication Type :
- Academic Journal
- Accession number :
- 16755255
- Full Text :
- https://doi.org/10.1097/01.CCM.0000227173.13497.56