Abstract
Treatment of primary cultures of rat ovarian dispersates with IL-1β results in morphologic and cytotoxic changes, thought to reflect tissue remodeling events associated with ovulation. We examined the role that the free radical nitric oxide plays in this process and report that IL-1β induces expression of the inducible isoform of nitric oxide synthase in ovarian cells as demonstrated by immunoprecipitation. We show that IL-1β treatment results in the formation of nitric oxide (as measured by accumulation of nitrite and cGMP) in both a time- and concentration-dependent manner that is prevented by aminoguanidine, a selective inhibitor of the inducible isoform of nitric oxide synthase. Aminoguanidine also inhibits IL-1-induced ovarian cellular cytotoxicity. These results suggest that nitric oxide is an important mediator of cell death and may act as a physiologically significant mediator of tissue remodeling events that occur in vivo during the ovulatory process.
Original language | English |
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Pages (from-to) | 3053-3056 |
Number of pages | 4 |
Journal | Journal of Clinical Investigation |
Volume | 92 |
Issue number | 6 |
State | Published - Dec 1993 |
Externally published | Yes |
Keywords
- Aminoguanidine
- Cytokines
- Interleukin-1
- Nitric oxide synthase
- Ovulation