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Ecotoxicol Environ Saf. 2002 Jun;52(2):117-22.
Effect of mercury on general and reproductive health of largemouth bass (Micropterus salmoides) from three lakes in New Jersey.

Friedmann AS, Costain EK, MacLatchy DL, Stansley W, Washuta EJ.

Division of Reproductive Biology, Johns Hopkins University, 615 North Wolfe Street, Baltimore, MD 21205, USA. andrew.friedmantate.ma.us

The influence of mercury on the general and reproductive health of wild fish populations has not been well studied. Therefore, a variety of health and reproductive indicators were measured in male largemouth bass (Micropterus salmoides) collected from three bodies of water in New Jersey: Assunpink Lake, Manasquan Reservoir, and Atlantic City Reservoir. The mean mercury content in fish muscle from Assunpink Lake was 0.30 microg/g; from Manasquan Reservoir, 1.23 microg/g; and from Atlantic City Reservoir, 5.42 microg/g. Body weight, length, condition factor, and gonadosomatic index were similar for all three lakes. Furthermore, there was no significant relationship between muscle mercury content and adrenocortical function, indicated by interrenal nuclear diameter and serum cortisol levels following stress. Bass from the Atlantic City Reservoir had a slightly lower, although significant, liver somatic index than bass from the two other lakes. A significant, positive correlation between 11-ketotestosterone serum concentrations and mercury muscle content was detected, although no significant relationship between testosterone serum concentrations and mercury muscle content was found. The findings of this study suggest that, while elevated levels of mercury in fish potentially alter androgen profiles, they do not substantially decrease other indicators of general and reproductive health. (c) 2002 Elsevier Science (USA).

online pharmacy ref. source: www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12061827&dopt=Abstract

Physiol Behav. 2002 Apr 1;75(4):541-9.
Effects of withdrawal from anabolic androgenic steroids on aggression in adult male rats.

McGinnis MY, Lumia AR, Possidente BP.

Department of Cell Biology and Anatomy, Mount Sinai School of Medicine, New York, NY 10029, USA. marilyn.mcginnissm.edu

In gonadally intact male rats, chronic exposure to high levels of testosterone propionate (TP) increases aggression, nandrolone (ND) has little effect and stanozolol (ST) suppresses aggression. The present experiment tested whether the effects of TP, ND and ST on aggression and reproductive tissues are reversed following anabolic androgenic steroid (AAS) withdrawal. Gonadally intact males received TP, ND, ST or vehicle for 12 weeks. Injections were then discontinued. Aggression was tested 3 weeks (short term) and 12 weeks (long term) after withdrawal of AAS treatment, with either a gonadally intact or a castrated opponent in three different environments (home, opponent's and neutral cage). After short-term withdrawal, some parameters of aggression were significantly above control levels in TP males. There were no significant differences between ND or ST males and controls, though ST males showed the lowest levels of aggression. No significant differences between any of the groups were found after long-term withdrawal. Eighteen weeks after AAS withdrawal, serum testosterone (T) and LH levels were comparable to controls in all groups. Testes weights were at control levels in ST males, but significantly higher than controls in TP and ND males. Seminal vesicle weights were significantly elevated in TP males, but similar to controls in both ND and ST males. None of the prostate weights were significantly different from controls. These results suggest that aggression gradually returns to normal following withdrawal from AAS. Some, if not all, hormone levels and tissue weights return to normal, suggesting possible long-lasting effects of chronic AAS exposure.

online pharmacy ref. source: www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12062318&dopt=Abstract

Toxicology. 2002 Jul 1;176(1-2):91-100.
Troglitazone enhances the hepatotoxicity of acetaminophen by inducing CYP3A in rats.

Li J, Kaneko T, Wang Y, Qin LQ, Wang PY, Sato A.

Department of Environmental Health, Medical University of Yamanashi, Yamanashi Tamaho 409-3898, Japan.

Troglitazone (TRZ) is the first of a new group of oral antidiabetic drugs, the thiazolidinediones, and is proven to lower plasma glucose levels in patients with type 2 diabetes mellitus. However, the concern has been raised because of several reports, in which severe hepatic dysfunction leading to hepatic failure was demonstrated in a few patients receiving the drug. We studied the effects of TRZ on the hepatotoxicity of carbon tetrachloride (CCl(4)) and acetaminophen (APAP) in rats, both of which exert their toxic effects through bioactivation associated with cytochrome P450 3A (CYP3A) and 2E1 (CYP2E1).Male standard (Wistar/ST) and type 2 diabetic model (GK/Jal) rats were kept on a powdered chow diet containing 0, 100, 500 mg/kg/rat of TRZ. Three weeks later, the rats were either sacrificed for an in vitro metabolism study or challenged with 0.50 g/kg CCl(4) p.o. or 0.75 g/kg APAP i.p.TRZ at 100 and 500 mg/kg/rat increased the CYP3A level as well as the testosterone 6beta-hydroxylation activities in liver microsomes, but did not affect CYP2E1. TRZ also enhanced APAP hepatotoxicity, as evidenced by significantly increased levels of alanine aminotransferase, aspartate aminotransferase and alpha-glutathione S-transferase in the plasma of rats, and by significantly low hepatic glutathione concentration.Our study demonstrated that high doses of TRZ can enhance hepatotoxicity of APAP in Wistar/ST and GK/Jal by inducing hepatic CYP3A.

online pharmacy ref. source: www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12062933&dopt=Abstract

Horm Metab Res. 2002 May;34(5):223-8.
Intrinsic regional differences in androgen receptors and dihydrotestosterone metabolism in human preadipocytes.

Joyner J, Hutley L, Cameron D.

Department of Diabetes and Endocrinology, Princess Alexandra Hospital, Ipswich Road, Wolloongabba 4102, Queensland, Australia. julie_joyneealth.qld.gov.au

Androgens play an important role in regulating the central obesity that is a strong risk factor for cardiovascular disease and insulin resistance. This study confirms that androgen receptors are present in subcultured human preadipocytes, with androgen receptor gene expression and saturable specific dihydrotestosterone binding, dissociation constant 1.02 - 2.56 nM and maximal binding capacity 30.8 - 55.7 fmol/mg protein. There was an intrinsic regional difference in androgen receptor complement, with more androgen receptors in visceral than in subcutaneous preadipocytes. Dihydrotestosterone was metabolised by human preadipocytes, with more androstanediol produced by subcutaneous than visceral preadipocytes. While dihydrotestosterone metabolism was insufficient to explain the regional variation in androgen binding, both of these differences would reduce the androgen responsiveness of the subcutaneous preadipocytes compared with visceral preadipocytes. There were no gender differences in androgen binding or metabolism. While the direct effects of androgens on human PAs remain uncertain, these regional differences suggest that AR-mediated regulation of certain PA functions influences adipose tissue distribution.

online pharmacy ref. source: www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12063633&dopt=Abstract

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