Effect of TCDD on corpus cavernosum histology and smooth muscle physiology
- 1 June 2004
- journal article
- Published by Springer Nature in International Journal Of Impotence Research
- Vol. 16 (3) , 224-230
- https://doi.org/10.1038/sj.ijir.3901060
Abstract
A polyhalogenated aromatic hydrocarbon, 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), is one of the most potent toxic environmental pollutants. Decreases in spermatogenesis and the ability to conceive and carry a pregnancy to term are the most sensitive signs of reproductive toxicity by TCDD in the mammal, but no report of its effect on the erectile function exists. We performed this study to investigate the effect of TCDD on the erectile function. New Zealand white rabbits were treated intraperitoneally with 1 g/kg of TCDD. At 4 (Gr I) and 8 (Gr II) weeks after the administration of TCDD, cavernosal tissues were harvested for strip study in the organ bath and testes were prepared for histologic examination. Compared to the maximal amplitude of 17.14.12 mN in normal control (Gr III), the contractions to cumulative concentrations of NE (10-8–10-4 M) were significantly decreased to 6.571.34 and 5.451.01 mN in Groups I and II, respectively. Compared to 51.127.38% in Gr III, relaxation to cumulative concentration (10-8–10-4 M) of acetylcholine was significantly decreased to 17.252.17% (Gr I) and 9.732.17% (Gr II) at a concentration of 10-4 M, respectively. Compared to 75.1213.18% in Gr III, relaxation to cumulative concentration (10-8–10-4 M) of SNP was significantly decreased to 31.497.89% (Gr I) and 18.546.12% (Gr II) at a concentration of 10-4 M, respectively. Histologically, intracavernosal fibrosis, abnormal subtunical deposition of fat and decreased sinusoidal space with consequent increase of trabecular smooth muscle contents were identified in TCDD-treated groups. In TCDD-treated animals, seminiferous tubules showed a decrease of germ cells with vacuolar degeneration and apoptotic cells. Spermatids were hardly seen. These results suggest that TCDD inhibits spermatogenesis and has a potential harmful effect on erectile function via changes of corpus cavernosum histology and smooth muscle physiology.Keywords
This publication has 23 references indexed in Scilit:
- In Uteroand Lactational Exposure of the Male Rat to 2,3,7,8-Tetrachlorodibenzo-p-dioxin Impairs Prostate DevelopmentToxicology and Applied Pharmacology, 1998
- In Uteroand Lactational Exposure of the Male Rat to 2,3,7,8-Tetrachlorodibenzo-p-dioxin Impairs Prostate Development: 2. Effects on Growth and CytodifferentiationToxicology and Applied Pharmacology, 1998
- Correlation of 2,3,7,8-Tetrachlorodibenzo-p-dioxin-Induced Apoptotic Cell Death in the Embryonic Vasculature with EmbryotoxicityToxicology and Applied Pharmacology, 1998
- The effects of testosterone on the cavernous tissue and erectile functionWorld Journal of Urology, 1997
- Early Life Stage Toxicity of 2,3,7,8-Tetrachlorodibenzo-p-dioxin in Zebrafish (Danio rerio)Toxicology and Applied Pharmacology, 1997
- Reduced Leydig cell volume and function in adult rats exposed to 2,3,7,8-tetrachlorodibenzo-p-dioxin without a significant effect on spermatogenesisToxicology, 1992
- Reproductive toxicity and toxicokinetics of 2,3,7,8-tetrachlorodibenzo-p-dioxinArchives of Toxicology, 1992
- Comparative Toxicology and Mechanism of Action of Polychlorinated Dibenzo-P-Dioxins and DibenzofuransAnnual Review of Pharmacology and Toxicology, 1986
- 2,3,7,8-Tetrachlorodibenzo-p-Dioxin and Related Halogenated Aromatic Hydrocarbons: Examination of the Mechanism of ToxicityAnnual Review of Pharmacology and Toxicology, 1982