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Temporal variations in chloroform-induced hepatotoxicity in rats
Toxicology
|March 1, 1983
Summary
Chloroform (CHCl3) hepatotoxicity in rats varies significantly with administration time, influenced by biological rhythms. Peak toxicity occurred with 21:00 h injections, while fasting exacerbated effects.
Area of Science:
- Pharmacology
- Toxicology
- Chronobiology
Background:
- Biological rhythms influence drug metabolism and efficacy.
- Understanding temporal variations in chemical toxicity is crucial for occupational health.
Purpose of the Study:
- To investigate the time-dependent effects of chloroform (CHCl3) induced acute hepatotoxicity in male Sprague-Dawley rats.
- To determine if the timing of CHCl3 administration affects liver damage markers.
Main Methods:
- Rats received a single intraperitoneal dose of CHCl3 or saline at different times (09:00, 13:00, 17:00, 21:00, 03:00).
- Hepatotoxicity was assessed 4 hours post-injection using serum enzymes (SGPT, SGOT, LDH) and liver glucose-6-phosphatase (G6Pase) activity.
- The impact of 16-hour fasting prior to CHCl3 injection was also evaluated.
Main Results:
- CHCl3 administration at 21:00 h resulted in maximal increases in SGPT, SGOT, and LDH.
- G6Pase activity was significantly depressed when CHCl3 was administered at 03:00 h and 13:00 h.
- Fasting for 16 hours before 09:00 h CHCl3 injection substantially increased hepatotoxicity.
Conclusions:
- The time of day significantly modulates CHCl3 induced hepatotoxicity in rats, linked to biological rhythms.
- Findings suggest potential relevance for industrial workers exposed to CHCl3 at different times.
- Chronotoxicity of CHCl3 should be considered in risk assessment and management strategies.