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Vol. 282, Issue 2, 521-527, 1997
Department of Biochemistry and Molecular Biology, University of
Miami School of Medicine, Miami, Florida
Evidence suggests the existence of multiple interactions between
dopamine, glutamate and nitric oxide (NO) in brain structures associated with psychomotor stimulation. The present study was undertaken to investigate the effect of the relatively selective inhibitor of the neuronal nitric oxide synthase (NOS) isoform, 7-nitroindazole (7-NI), on the development of sensitization to the
locomotor stimulating effect of cocaine and methamphetamine (METH).
Male Swiss Webster mice that received 15 mg/kg cocaine once a day for 5 days developed a marked locomotor sensitization to a challenge cocaine
(15 mg/kg) or cross-sensitization to a challenge METH (0.5 mg/kg)
injection given after a 10-day drug-free period. This treatment also
produced a context-dependent sensitization as evident by the sensitized
response to a challenge saline injection. Pretreatment with 7-NI (25 mg/kg) 30 min before cocaine administration (5 days) completely blocked
the induction of sensitization to cocaine, the cross-sensitization to
METH and the conditioned locomotion induced by cocaine. 7-NI when given
alone, either acutely or for 5 days, had no significant effect on the
locomotor activity of animals. Animals treated with METH (1.0 mg/kg)
for 5 days developed marked sensitization to challenge METH (0.5 mg/kg), cross-sensitization to challenge cocaine (15 mg/kg) and
context-dependent locomotion. Pretreatment with 7-NI (25 mg/kg)
attenuated the sensitized response to METH and the cross-sensitization
to cocaine as revealed after a 10-day drug-free period. However, the
METH-induced conditioned locomotion was unaffected by the pretreatment
with 7-NI. The present study supports the role of brain NO in the
development of sensitization to both psychostimulants, cocaine and
METH. However, it appears that the inability of 7-NI to completely
abolish the sensitized responses induced after METH administration is
the result of the resistible conditioned locomotion caused by METH, but
not by cocaine.
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