Exposure to di(n-butyl)phthalate and benzo(a)pyrene alters IL-1β secretion and subset expression of testicular macrophages, resulting in decreased testosterone production in rats

• Published in: Toxicology and applied pharmacology Vol. 248; no. 1; pp. 28 - 37
• Main Authors: Zheng, Shan-jun, Tian, Huai-jun, Cao, Jia, Gao, Yu-qi
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier Inc 01.10.2010; Elsevier
• Subjects: Animals; Benzo(a)pyrene; Benzo(a)pyrene - toxicity; Biological and medical sciences; Co-exposure; Di(n-butyl)phthalate; Dibutyl Phthalate - toxicity; Drug Interactions; Endocrine Disruptors - toxicity; IL-1β; Interleukin-1beta - drug effects; Interleukin-1beta - secretion; Macrophages - drug effects; Macrophages - metabolism; Male; Medical sciences; Rats; Rats, Sprague-Dawley; Testicular macrophages; Testis - drug effects; Testis - metabolism; Testosterone; Testosterone - biosynthesis; Testosterone - metabolism; Toxicology; Testosterone; Testicular macrophages; Benzo(a)pyrene; IL-1β; Co-exposure; Di(n-butyl)phthalate; Rat; Toxicity; Biosynthesis; Phthalate; Testicle; Toxic association; Testicular hormone; Androgen; Secretion; Cytokine; Rodentia; Interleukin 1β; Exposure; Male genital system; Vertebrata; Mammalia; Animal; Sex steroid hormone; Macrophage
• ISSN: 0041-008X; 1096-0333
• DOI: 10.1016/j.taap.2010.07.008

Di(n-butyl)phthalate (DBP) and benzo(a)pyrene (BaP) are environmental endocrine disruptors that are potentially hazardous to humans. These chemicals affect testicular macrophage immuno-endocrine function and testosterone production. However, the underlying mechanisms for these effects are not fully understood. It is well known that interleukin-1 beta (IL-1β), which is secreted by testicular macrophages, plays a trigger role in regulating Leydig cell steroidogenesis. The purpose of this study was to reveal the effects of co-exposure to DBP and BaP on testicular macrophage subset expression, IL-1β secretion and testosterone production. Adult male Sprague–Dawley rats were randomly divided into seven groups; two groups received DBP plus BaP (DBP + BaP: 50 + 1 or 250 + 5 mg/kg/day) four groups received DBP or BaP alone (DBP: 50 or 250 mg/kg/day; BaP: 1 or 5 mg/kg/day), and one group received vehicle alone (control). After co-exposure for 90 days, the relative expression of macrophage subsets and their functions changed. ED2 + testicular macrophages (reactive with a differentiation-related antigen present on the resident macrophages) were activated and IL-1β secretion was enhanced. DBP and BaP acted additively, as demonstrated by greater IL-1β secretion relative to each compound alone. These observations suggest that exposure to DBP plus BaP exerted greater suppression on testosterone production compared with each compound alone. The altered balance in the subsets of testicular macrophages and the enhanced ability of resident testicular macrophages to secrete IL-1β, resulted in enhanced production of IL-1β as a potent steroidogenesis repressor. This may represent an important mechanism by which DBP and BaP repress steroidogenesis.