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Cimetidine (Tagamet) Is a Reproductive Toxicant in Male Rats Affecting Peritubular Cells¹

^c Laboratory of Cellular Biology, Department of Morphology, Federal University of Minas Gerais, Brazil ^d Department of Morphology, Federal University of Sao Paulo, UNIFESP, Sao Paulo, Brazil ^e Apoptosis Laboratory, Department of Pathology, Federal University of Minas Gerais, Minas Gerais, Brazil ^f Department of Physiology, Southern Illinois University, School of Medicine, Carbondale, Illinois 62901-6512

Cimetidine (Tagamet) is a potent histaminic H2-receptor antagonist, extensively prescribed for ulcers and now available without prescription. Cimetidine is a known testicular toxicant, but its mechanism of action remains uncertain. Rats were treated i.p. with cimetidine either at 50 mg/kg or 250 mg/kg body weight for 59 days. Accessory sex organ weights, but not testis weight, were significantly reduced in the high dose treated groups. FSH levels were significantly elevated in both treated groups, but testosterone levels were unchanged. A high degree of variability characterized testis histology, with most tubules appearing normal and some tubules (15–17%) partially lacking or devoid of germ cells. Morphometry showed that although seminiferous tubule volume was not significantly changed, the volume of peritubular tissue was reduced in the high dose group. There was extensive duplication of the basal lamina, lamina densa in both apparently normal spermatogenic tubules and severely damaged tubules. Apoptotic peritubular myoid cells were also found. TUNEL labeling confirmed extensive apoptotic cell death in peritubular cells, but revealed apoptosis of vascular smooth muscle. Given that 1) peritubular myoid cell apoptosis occurs in apparently normal tubules, that 2) basal lamina disorders are found, and that 3) peritubular cells are lost from the testis, it is suggested that the primary event in cimetidine-related damage is targeted to testicular smooth muscle cells. This is the first in vivo-administered toxicant to be described that targets myoid cells, resulting in abnormal spermatogenesis.

First decision: 14 March 2000.

¹ This work was supported by NIH HD35494.

² Correspondence. FAX: 618 453 1517; lrussell{at}siumed.edu

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