The effects of Nω-nitro-L-arginine methyl ester(L-NAME)i.v.and nitric oxide(NO) inhalation on integrated systemic responses to cocaine were studied in lightly anesthetized, paralyzed, and mechanically ventilated rats...The effects of Nω-nitro-L-arginine methyl ester(L-NAME)i.v.and nitric oxide(NO) inhalation on integrated systemic responses to cocaine were studied in lightly anesthetized, paralyzed, and mechanically ventilated rats.Cocaine [4 mg/(kg. min) i.v.] produccd seizures then isoelectric electrocephalographic(isoEEG)activity as well as an initial increase in systolic blood pressure and heart rate,then progressive cardiovascular system depression culminating in asystole. Pretreatment with L-NAME[2 mg/(kg. min)i.v. ] for 30 min significantly reduced the incidence of seizure as compared to saline treated animals (saline 7/8; L-NAME 3/8).Doses of cocaine that produced arrhythmias, isoEEG and asystole were significantly lower in the L-NAME treated animals as compared to the saline group. L-NAME did not affect peak systolic blood pressure and heart rate responses to cocaine. NO inhalation(80 ppm)did not affect CNS and cardiovascular responses to cocaine in control animals but enhanced the effects of L-NAME on cocaine toxicity. The results show that pretreatment with L-NAME reduces the central nervous system stimulatory effect of cocaine (reduced seizure incidence) and enhances its depressant effect on both the central nervous system (lower does for isoEEG) and the cardiovascular stimulatory action of cocaine. NO inhalation does not protect against any of the systemic effects of cocaine in animals with normal or suppressed NO production.展开更多
文摘The effects of Nω-nitro-L-arginine methyl ester(L-NAME)i.v.and nitric oxide(NO) inhalation on integrated systemic responses to cocaine were studied in lightly anesthetized, paralyzed, and mechanically ventilated rats.Cocaine [4 mg/(kg. min) i.v.] produccd seizures then isoelectric electrocephalographic(isoEEG)activity as well as an initial increase in systolic blood pressure and heart rate,then progressive cardiovascular system depression culminating in asystole. Pretreatment with L-NAME[2 mg/(kg. min)i.v. ] for 30 min significantly reduced the incidence of seizure as compared to saline treated animals (saline 7/8; L-NAME 3/8).Doses of cocaine that produced arrhythmias, isoEEG and asystole were significantly lower in the L-NAME treated animals as compared to the saline group. L-NAME did not affect peak systolic blood pressure and heart rate responses to cocaine. NO inhalation(80 ppm)did not affect CNS and cardiovascular responses to cocaine in control animals but enhanced the effects of L-NAME on cocaine toxicity. The results show that pretreatment with L-NAME reduces the central nervous system stimulatory effect of cocaine (reduced seizure incidence) and enhances its depressant effect on both the central nervous system (lower does for isoEEG) and the cardiovascular stimulatory action of cocaine. NO inhalation does not protect against any of the systemic effects of cocaine in animals with normal or suppressed NO production.
