Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1997 Apr;56(4):705-12.
doi: 10.1016/s0091-3057(96)00408-x.

Modulation of vigilance and behavioral activation by alpha-1 adrenoceptors in the rat

Affiliations

Modulation of vigilance and behavioral activation by alpha-1 adrenoceptors in the rat

T Puumala et al. Pharmacol Biochem Behav. 1997 Apr.

Abstract

This study investigated the role of alpha-1 adrenergic receptors in the modulation of attention and behavioral activity by assessing the effects of alpha-1 adrenergic receptor stimulation or blockade on the performance of rats in tasks involving vigilance (sustained attention) and selective attention [five-choice serial reaction time (5-CSRT)]. Pretesting subcutaneous administration of St-587 (a putative alpha-1 agonist) at 100 micrograms/kg, but not at 300 or 1000 micrograms/kg, significantly improved the choice accuracy of rats in the 5-CSRT task (monitoring of visual stimuli), whereas prazosin (a prototype alpha-1 antagonist) at 300 micrograms/kg administered subcutaneously slightly impaired choice accuracy of the rats in this task. Prazosin at 100 micrograms/kg blocked the ability of St-587 at 100 micrograms/kg to improve choice accuracy. Furthermore, St-587 at 100 micrograms/kg significantly increased the number of trials completed and reduced the probability of premature responses, whereas prazosin at 300 micrograms/kg decreased the number of trials completed and the latency of animals to make correct responses in the task. Prazosin at 100 micrograms/kg blocked the effect of St-587 at 100 micrograms/kg in increasing the number of trials completed. However, prazosin at 100 micrograms/kg did not abolish the effect of St-587 in reducing the probability of premature responses. Because the effect of St-587 at 100 micrograms/kg in improving choice accuracy is rather modest, it is possible that when the 100- and 300-microgram/kg doses of St-587 were administered in a counterbalanced order, this effect could have been overlooked due to day-to-day variation. Thus, the present results suggest that stimulation of alpha-1 adrenergic receptors can facilitate vigilance.

PubMed Disclaimer

Publication types

LinkOut - more resources