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
. 1971 Nov;43(3):504-13.
doi: 10.1111/j.1476-5381.1971.tb07181.x.

Effect of receptor blocking drugs on the depletion of brain glycogen by amphetamine

Effect of receptor blocking drugs on the depletion of brain glycogen by amphetamine

D A Hutchins et al. Br J Pharmacol. 1971 Nov.

Abstract

1. Amphetamine sulphate (5 mg/kg), administered intraperitoneally, reduces the concentration of glycogen in the mouse brain by 25-30% after 30 minutes.2. The effect of several receptor blocking drugs on the amphetamine-induced cerebral glycogenolysis was studied.3. DL-Propranolol (0.25 mg/kg) and pronethalol (10 mg/kg) antagonized the depletion of brain glycogen by amphetamine.4. Phentolamine, methysergide, atropine and mepyramine failed to antagonize the amphetamine-induced glycogenolysis.5. D-Propranolol, chlorpromazine and phenoxybenzamine antagonized the glycogenolytic effect of amphetamine only when administered in sedative doses.6. It is concluded that amphetamine-induced glycogenolysis in the mouse brain may be mediated through a beta-adrenoceptor.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Lancet. 1967 May 27;1(7500):1135-7 - PubMed
    1. Biochem Pharmacol. 1969 Oct;18(10):2599-604 - PubMed
    1. Br J Pharmacol Chemother. 1964 Apr;22:267-74 - PubMed
    1. J Pharmacol Exp Ther. 1965 Jul;149:43-9 - PubMed
    1. J Pharm Pharmacol. 1969 Apr;21(4):241-7 - PubMed

MeSH terms

LinkOut - more resources