AbstractsBiology & Animal Science

The biological function of nitric oxide and its oxidized forms has received a great deal of attention over the past two decades. However much less attention has been focused on the reduced nitric oxide, nitroxyl (HNO). Unlike NO, HNO is highly reactive species and thus it needs to be generated by using donor compounds under experimental conditions. Currently there is only one donor available, Angeli s salt, which releases HNO in a controlled fashion under pysiological conditions. Prior studies have shown the pro-oxidative and cytotoxic potential of Angeli s salt compared to NO donors. The high reactivity of HNO with cysteine thiols is considered to form the biochemical basis for its unique properties compared to other nitrogen oxides. Such thiol modification cold result in disturbances of vital cellular functions and subsequently to death of disturbance sensitive cells, such as neurons. Therefore modification of proteins and lipids was studied in vitro and the potential neurotoxicity was studied in vivo by local infusion of Angeli s salt into the rat central nervous system. The results show that under aerobic in vitro conditions, HNO can, subsequent to autoxidation, cause irreversible oxidative modification of proteins and lipids. These effects are not however seen in cell culture or following infusion of Angeli s salt directly into the rat central nervous tissue likely due to presence of lower oxygen and higher thiol concentration. However, due to high reactivity with thiols, HNO can cause irreversible inactivation of cysteine modification sensitive enzymes such as cysteine proteases papain in vitro and cathepsin B in cell culture. Furthermore it was shown that infusion of HNO releasing Angeli s salt into the rat central nervous system causes necrotic cell death and motor dysfunction following infusion into the lumbal intrathecal space. In conclusion, the acute neurotoxic potential of Angeli s salt was shown to be relatively low, but still higher compared to NO donors. HNO was shown to affect numerous cellular processes which could result in neurotoxicity if HNO was produced in vivo. Typpioksidin (NO) ja sen hapetustuotteiden biologisia ominaisuuksia on tutkittu laajalti viime vuosikymmeninä ja niiden on osoitettu osallistuvan elimistön normaalin toiminnan säätelyyn. Toisaalta NO:n tai sen johdoksien tuotanto on lisääntynyt lukuisissa elimistön kannalta haitallisissa tiloissa, kuten ALS:n ja Parkinsonin taudin kaltaisissa hermostorappeumasairauksissa. Toisin kuin NO:n ja sen hapetustuotteiden ominaisuuksia, NO:n pelkistyneen muodon, nitroksyylin (HNO/NO-), biologisia ominaisuuksia ei ole juurikaan kartoitettu. NO:hon verrattuna nitroksyyli on erittäin reaktiivista, mikä vaikeuttaa sen mittaamista eikä tänä päivänä tiedetä varmuudella muodostuuko sitä elimistössä vai ei. Koeputkiolosuhteissa on osoitettu NO:ta normaalisti tuottavan typpioksidisyntaasin pystyvän tuottamaan myös nitroksyyliä. Koska varmuutta nitroksyylin tuotannosta elimistössä ei ole, joudutaan kokeellisissa tutkimuksissa käyttämään…