Literature DB >> 9329124

Flutamide: a novel agent for restoring the depressed cell-mediated immunity following soft-tissue trauma and hemorrhagic shock.

M W Wichmann1, M K Angele, A Ayala, W G Cioffi, I H Chaudry.   

Abstract

Recent studies indicate beneficial effects of androgen depletion in male mice, before trauma-hemorrhage on cell-mediated immunity following soft-tissue trauma and hemorrhagic shock. Nonetheless, it remains unknown whether androgen receptor blockade following the insult has any salutary effects. To study this, male C3H/HeN mice were either sham-operated or subjected to soft-tissue trauma (i.e., 2.5 cm midline laparotomy) followed by hemorrhagic shock (blood pressure 35 +/- 5 mmHg for 90 min) and then adequately resuscitated (shed blood and lactated Ringer's). Immediately after the completion of resuscitation, as well as 24 and 48 h thereafter, the animals received either vehicle, 10 mg/kg body weight (BW) flutamide or 25 mg/kg BW flutamide subcutaneously. At 72 h after resuscitation, all animals were killed. The spleens and peritoneal macrophages (M phi) were then harvested and cultures established to determine IL-2 and IL-3 release, splenocyte proliferative capacity, as well as splenic and peritoneal M phi IL-1 release. Moreover, plasma testosterone and corticosterone levels were measured. Our results indicate that trauma-hemorrhage resulted in significant depression of splenocyte and M phi functions in vehicle-treated and animals receiving 10 mg/kg BW flutamide. Treatment with 25 mg/kg BW flutamide following trauma-hemorrhage, however, resulted in levels of cytokine release which were comparable with those found in sham-operated animals. No significant alterations in plasma corticosterone and testosterone levels were observed in any of the experimental groups. These findings indicate that short-term therapy of males with the androgen receptor blocker, flutamide at 25 mg/kg BW, following trauma-hemorrhage has protective effects on immune functions. This protective effect is dose dependent, since 10 mg/kg BW flutamide did not produce significant salutary effects. Thus, flutamide represents a novel and safe agent for improving the depressed functions in male trauma patients suffering severe blood loss.

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Year:  1997        PMID: 9329124

Source DB:  PubMed          Journal:  Shock        ISSN: 1073-2322            Impact factor:   3.454


  23 in total

1.  Female sex hormones regulate macrophage function after trauma-hemorrhage and prevent increased death rate from subsequent sepsis.

Authors:  Markus W Knöferl; Martin K Angele; Michael D Diodato; Martin G Schwacha; Alfred Ayala; William G Cioffi; Kirby I Bland; Irshad H Chaudry
Journal:  Ann Surg       Date:  2002-01       Impact factor: 12.969

Review 2.  Gender dimorphism in immune responses following trauma and hemorrhage.

Authors:  Yukihiro Yokoyama; Martin G Schwacha; T S Anantha Samy; Kirby I Bland; Irshad H Chaudry
Journal:  Immunol Res       Date:  2002       Impact factor: 2.829

Review 3.  Which gender is better positioned in the process of liver surgery? Male or female?

Authors:  Yukihiro Yokoyama; Masato Nagino; Yuji Nimura
Journal:  Surg Today       Date:  2007-09-26       Impact factor: 2.549

4.  Mitogen activated protein kinase (MAPK) mediates non-genomic pathway of estrogen on T cell cytokine production following trauma-hemorrhage.

Authors:  Takao Suzuki; Huang-Ping Yu; Ya-Ching Hsieh; Mashkoor A Choudhry; Kirby I Bland; Irshad H Chaudry
Journal:  Cytokine       Date:  2008-03-14       Impact factor: 3.861

Review 5.  Surgical trauma and immunosuppression: pathophysiology and potential immunomodulatory approaches.

Authors:  Martin K Angele; Irshad H Chaudry
Journal:  Langenbecks Arch Surg       Date:  2005-07-02       Impact factor: 3.445

6.  Gender and acute respiratory distress syndrome in critically injured adults: a prospective study.

Authors:  Daithi S Heffernan; Lesly A Dossett; Michelle A Lightfoot; Richard D Fremont; Lorraine B Ware; Robert G Sawyer; Addison K May
Journal:  J Trauma       Date:  2011-10

7.  Flutamide attenuates pro-inflammatory cytokine production and hepatic injury following trauma-hemorrhage via estrogen receptor-related pathway.

Authors:  Tomoharu Shimizu; Huang-Ping Yu; Ya-Ching Hsieh; Mashkoor A Choudhry; Takao Suzuki; Kirby I Bland; Irshad H Chaudry
Journal:  Ann Surg       Date:  2007-02       Impact factor: 12.969

Review 8.  The role of estrogen and receptor agonists in maintaining organ function after trauma-hemorrhage.

Authors:  Huang-Ping Yu; Irshad H Chaudry
Journal:  Shock       Date:  2009-03       Impact factor: 3.454

9.  Testosterone depletion by castration may protect mice from heat-induced multiple organ damage and lethality.

Authors:  Chian-Yuh Lin; Mao-Tsun Lin; Ruei-Tang Cheng; Sheng-Hsien Chen
Journal:  J Biomed Biotechnol       Date:  2010-04-12

Review 10.  Estrogen: a novel therapeutic adjunct for the treatment of trauma-hemorrhage-induced immunological alterations.

Authors:  Raghavan Raju; Kirby I Bland; Irshad H Chaudry
Journal:  Mol Med       Date:  2008 Mar-Apr       Impact factor: 6.354

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