Alterations in Endocrine Responses in Male Sprague-Dawley Rats following Oral Administration of Methyl tert-Butyl Ether

• Published in: Toxicological sciences Vol. 54; no. 1; pp. 168 - 176
• Main Authors: Williams, Tracy M., Cattley, Russell C., Borghoff, Susan J.
• Format: Journal Article
• Language: English
• Published: Cary, NC Oxford University Press 01.03.2000
• Subjects: Administration, Oral; Air Pollutants - toxicity; Animals; Biological and medical sciences; Body Weight - drug effects; Carcinogenesis, carcinogens and anticarcinogens; Chemical agents; dihydrotestosterone; Endocrine System - drug effects; hormonal feedback; Hormones - blood; hypothalamus-pituitary-testicular axis (HPT); Kidney - pathology; Leydig cell tumors; liothyronine; Liver - pathology; luteinizing hormone; Male; Medical sciences; Methyl Ethers - toxicity; methyl tert-butyl ether (MTBE); Organ Size - drug effects; prolactin; Radioimmunoassay; Rats; Rats, Sprague-Dawley; Receptors, Cell Surface - agonists; Receptors, Cell Surface - antagonists & inhibitors; Receptors, Dopamine - drug effects; Steroids - biosynthesis; Testosterone - blood; Testosterone - metabolism; Thyroid Function Tests; Tumors; Endocrinopathy; Hormone; Rat; Toxicity; Rodentia; Hypothalamohypophysotesticular axis; Oral administration; Male; Endocrine disruptor; Testicle; Leydig cell; Multiple dose; Carcinogen; Vertebrata; Additive; Mammalia; Animal; Motor fuel; Mechanism of action; Male genital diseases
• ISSN: 1096-6080; 1096-0929; 1096-0929
• DOI: 10.1093/toxsci/54.1.168

Methyl tert-butyl ether (MTBE) is an oxygenated fuel additive used to decrease carbon monoxide emissions during combustion. MTBE is a nongenotoxic chemical that induces Leydig cell tumors (LCT) in male rats. The mechanism of MTBE-induced LCT is not known; however, LCT induced by other nongenotoxic chemicals have been associated with the disruption of the hypothalamus-pituitary-testicular (HPT) axis. The objective of this study was to determine whether MTBE functions as an endocrine-active compound by affecting levels of specific hormones involved in the maintenance of the HPT axis. Nine-week-old male Sprague-Dawley rats were administered MTBE by gavage at 0, 250, 500, 1000, or 1500 mg MTBE/kg/day for 15 or 28 consecutive days and sacrificed 1 h following the last dose. Relative testis weights were increased only in high-dose animals treated for 28 days, and no testicular lesions were observed at any dose level. Adrenal gland, liver, and kidney weights were also increased. Histologic changes included protein droplet nephropathy of the kidney and centrilobular hypertrophy of the liver. Interstitial fluid and serum testosterone levels as well as serum prolactin levels were decreased only in animals treated with 1500 mg MTBE/kg/day for 15 days. At 28 days, serum triiodothyronine (T3) was significantly decreased at 1000 and 1500 mg MTBE/kg/day compared to control animals, and a decrease in serum luteinizing hormone and dihydrotestosterone was observed at 1500 mg MTBE/kg/day. These results indicate that MTBE causes mild perturbations in T3 and prolactin; however, the changes in testosterone and LH levels did not fit the pattern caused by known Leydig cell tumorigens.