Thoreux-Manlay A, Vélez de la Calle J F, Olivier M F, Soufir J C, Masse R, Pinon-Lataillade G
Commissariat à l'Energie Atomique CEA, Département de Pathologie et Toxicologie Expérimentales, Fontenay-aux-Roses, France.
Toxicology. 1995 Jun 26;100(1-3):101-9. doi: 10.1016/0300-483x(95)03066-o.
To clarify the mechanism of the action of lead on male reproductive function, adult male rats were injected intraperitoneally (i.p.) with lead acetate (8 mg/kg/day of lead), 5 days a week for 35 days. Despite this high dose, germ cells and Sertoli cells did not appear to be major targets of lead. However, lead determination in the reproductive organs showed that the accessory sex glands are such a target. Epididymal function was unchanged. In lead-exposed rats, plasma and testicular testosterone dropped by about 80%, but plasma luteinizing hormone (LH) only dropped by 32%. After luteinizing hormone releasing hormone (LHRH) stimulation of the pituitary, the plasma LH level reached the control one, but plasma testosterone remained significantly reduced by 37%. The sharp decrease in the testosterone:LH ratio in lead-exposed rats, combined with the significant reduction of intertubular tissue volume in the testes, indicate impaired Leydig cell function.
