Mechanism of toxicity of precocene II in rat hepatocyte cultures

✍ Scribed by Hammond, Alison H. ;Garle, Michael J. ;Fry, Jeffrey R.

• Publisher: John Wiley and Sons
• Year: 1995
• Tongue: English
• Weight: 907 KB
• Volume: 10
• Category: Article
• ISSN: 0887-2082
• DOI: 10.1002/jbt.2570100507

✦ Synopsis

Precocene I1 was more toxic in 24 hour cultures than in 72 hour cultures of rat hepatocytes. In 24 hour cultures, there was no observable toxicity at 75 pM precocene I1 after exposure for 6 hours, but after 24 hours, 65% of the cells were dead. In contrast, although 794 pM killed 50% of the cells in the 72 hour cultures after a 24 hour exposure, 1 mM killed 96% of the cells within 6 hours. In both 24 and 72 hour cultures, cell death was preceded by a rapid, early loss of mitochondrial membrane potential, followed by decreases in glutathione, reduced pyridine nucleotide status, and plasma membrane Na+/K+-ATPase activity. There was also a rapid loss of ATP in the 72 hour cultures but not in the 24 hour cultures; therefore, onset of cell death may be closely linked to loss of ATP. In- hibition of cytochrome P-450 prevented the toxicity, and partially protected against the loss of membrane potential and glutathione, in 24 hour cultures but was ineffective in 72 hour cultures. Therefore, in addition to depletion of glutathione, precocene I1 appears to damage mitochondria and plasma membrane functions and can do so by more than one pathway.