Dehydroepiandrosterone affects Trypanosoma cruzi tissue parasite burdens in rats

• Published in: Acta tropica 2007-06, Vol.102 (3), p.143-150
• Main Authors: Santos, Carla Domingues, Toldo, Míriam Paula Alonso, Levy, Antonio Marcos Apparecida, Kawasse, Laura Midori, Zucoloto, Sérgio, do Prado, José Clóvis
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Chagas Disease - drug therapy; Chagas Disease - parasitology; Dehydroepiandrosterone; Dehydroepiandrosterone - pharmacology; Female; General aspects; Heart - parasitology; Infectious diseases; Lytic antibody; Macrophages, Peritoneal - drug effects; Macrophages, Peritoneal - parasitology; Male; Medical sciences; Parasitic diseases; Rats; Rats, Wistar; Tissue parasitism; Trypanosoma cruzi; Trypanosoma cruzi - drug effects
• ISSN: 0001-706X; 1873-6254
• DOI: 10.1016/j.actatropica.2007.04.010

Dehydroepiandrosterone (DHEA), the predominant steroid hormone produced by adrenal glands has significant effects on the immune system. DHEA enhances immune responses against a wide range of viral, bacterial, and parasitic pathogens. In the present study, we investigated the effects of DHEA treatment during the acute phase of experimental Trypanosoma cruzi infection. Male and female Wistar rats were infected with the Y strain of T. cruzi and treated subcutaneously with 40 mg/kg body weight/day of DHEA. Myocardial parasitism and inflammation were always present in the heart during the acute phase, in male and female infected animals, regardless of DHEA treatment, but the numbers of amastigote nests in cardiomyocytes were significantly lower in DHEA-treated rats. At the end of the acute phase, the nests became rare or virtually absent in all experimental infections. Histological analysis of the adrenal glands showed that treated males displayed an absence of parasites. DHEA treatment also resulted in reduced parasitisim of heart and adrenal glands, as indicated by fewer and smaller amastigote burdens, and less inflammatory infiltrate and tissue disorganization. DHEA treatment also resulted in thymic atrophy as measured both by reduced weight and by a reduction in the number of cultured activated thymocytes. In vitro analysis showed the number of activated macrophages was higher in treated animals. Antibody levels were monitored by complement-mediated lysis. Higher titers were observed in females when compared to males; but DHEA treatment enhanced the percentage of lysis for both sexes. These findings suggest that DHEA can play a role in the control of parasite multiplication.