Chronic stress induces strain-dependent sensitization to the behavioral effects of amphetamine in the mouse

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Abstract

Following 10 days of daily restraint stress, sensitization developed to the stimulatory effect of amphetamine on locomotion in DBA/2 but not in C57BL/6 mice tested 24 h after the last stressful experience regardless of their being naive or habituated to the test cages. Saline-injected C57BL/6 mice, however, showed an increase of locomotion 24 h after chronic stress treatment. Chronically stressed mice of the two strains did not exhibit any alteration of dopamine and metabolites (3-4-dihydroxyphenylacetic acid, homovanillic acid, and 3-methoxytyramine) levels in the frontal cortex, caudatus putamen, or nucleus accumbens septi, thus ruling out that stress-induced alteration of basal dopamine metabolism affected the behavioral response to amphetamine challenging in DBA/2 mice. Ten daily amphetamine injections (5 mg/kg) did not significantly modify the behavioral response to amphetamine in either strain of mice tested 24 h after the end of the chronic treatment and did not increase locomotion in saline-injected C57BL/6 mice. Finally, chronically stressed hybrids B6D2F1 did not show sensitization to the locomotor effects of amphetamine, suggesting a dominant mode of inheritance in the response to chronic stress of the C57BL/6 strain.

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Cited by (62)

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    Furthermore, analyzing the interaction examinations of the NAc shell and core, footshock-treatment-induced stress positively modulated and enhanced the MAMPH-induced behavioral sensitization in the acquisition and testing phases. The present data did not fully support the previous viewpoint that chronic stress sensitized the projections of the VTA to the NAc [10,34]. In particular, the NAc core under footshock stress inhibits behavioral sensitization, which data conflict with the previous viewpoint that chronic stress sensitized the neural pathway from the VTA to the NAc [10].

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    In fact, the desynchronization of circadian motor activity rhythm was markedly less pronounced in C57BL/6J than in DBA/2J mice. Because reactivity to stress distinguishes DBA/2J and C57BL/6J mice (Badiani et al., 1992; Cabib et al., 1988), this interstrain difference can also contribute to our data. In any case, dissociation clearly appears between the amplitude of the desynchronization of circadian motor activity rhythm and modifications induced in alcohol intake in DBA/2J mice (Rosenwasser et al., 2005).

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Present address: Department of Psychology, Concordia University, 1455 de Maisonneuve, Montreal, Quebec, Canada H3G 1M8

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