Alteration of testicular biochemistry during protein restriction in nickel treated rats.

Abstract

Nickel sulfate (2.0 mg/100 g.b.wt) dissolved in double-distilled water was administered (i.p.) on alternate days for ten doses to normal protein-fed and protein-restricted Wister strain albino rats (b.wt. 160 +/- 5 g). Two groups were used: one with normal protein diet, whereas the other with protein-restricted diet served as control. Twenty-four hours after the last treatment, the animals were sacrificed by decapitation. Tissues such as the testes, seminal vesicles, epididymis (Cauda and Caput) and prostate were dissected out, wiped clean, and stored at -20 degrees C until analysis. Lactate dehydrogenase (LDH) activities, glutamate oxaloacetate transaminase (GOT) activities, glycogen content, cholesterol content, and total protein content of the testes were estimated. Nickel sulfate administration significantly decreased the body weight of both normal protein-fed and protein-restricted groups of animals; the organ weights were also decreased. Significant decrease of LDH activity was observed, but GOT activity was not altered significantly. Testicular glycogen and cholesterol increased significantly in both experimental groups, but total protein content decreased. Nickel sulfate seems to have an adverse effect on the male reproductive system in both groups of animals fed with normal protein (18% casein) diet and protein restricted (5% casein) diet.

• Authors: K K Das, S Dasgupta
• Journal: Biological trace element research (Biol Trace Elem Res) Vol. 60 Issue 3 Pg. 243-9 (Dec 1997) ISSN: 0163-4984 [Print] United States
• PMID: 9494062 (Publication Type: Comparative Study, Journal Article)

Chemical References

• Irritants
• Proteins
• nickel sulfate
• Nickel
• Cholesterol
• L-Lactate Dehydrogenase
• Aspartate Aminotransferases
• Glutathione

Topics

• Animals
• Aspartate Aminotransferases (analysis)
• Body Weight (drug effects)
• Cholesterol (analysis)
• Diet, Protein-Restricted
• Epididymis (chemistry, drug effects, enzymology)
• Glutathione (analysis)
• Irritants (toxicity)
• L-Lactate Dehydrogenase (analysis)
• Male
• Nickel (toxicity)
• Organ Size (drug effects)
• Prostate (chemistry, drug effects, enzymology)
• Proteins (analysis)
• Rats
• Rats, Wistar
• Seminal Vesicles (chemistry, drug effects, enzymology)
• Testis (chemistry, drug effects, enzymology)