Abstract:
:NO has been identified recently as the prime islet-toxic product of inflammatory macrophages. The adverse effects of IL-1 on isolated islets also have been reported to involve NO. We now show that exposure of an islet cell suspension to the NO donor nitroprusside or to activated macrophages leads to DNA strand breaks. Macrophages did not induce DNA damage in the presence of the NO synthase inhibitor NG-methyl-L-arginine. DNA strand breaks were demonstrated at the level of single cells by a modified nick-translation procedure and confirmed by analysis of DNA fragmentation by gel electrophoresis. DNA strand breaks occurred within 1 h and preceded islet cell lysis. DNA damage could not be prevented by inhibitors of endogenous endonucleases. We conclude that islet cell DNA is an early target of NO action.
journal_name
Diabetesjournal_title
Diabetesauthors
Fehsel K,Jalowy A,Qi S,Burkart V,Hartmann B,Kolb Hdoi
10.2337/diab.42.3.496subject
Has Abstractpub_date
1993-03-01 00:00:00pages
496-500issue
3eissn
0012-1797issn
1939-327Xjournal_volume
42pub_type
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