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
. 1991 Apr 1;88(7):2802-6.
doi: 10.1073/pnas.88.7.2802.

Increased abundance of alternatively spliced forms of D2 dopamine receptor mRNA after denervation

Affiliations

Increased abundance of alternatively spliced forms of D2 dopamine receptor mRNA after denervation

K A Neve et al. Proc Natl Acad Sci U S A. .

Abstract

The existence of two molecular forms of D2 dopamine receptors suggests that differences in the distribution or regulation of the two forms could be exploited for the pharmacological treatment of disease. Using probes selective for each alternatively spliced variant of D2 receptor mRNA, we determined that both variants were widely distributed in rat brain and pituitary but that the ratio of the forms varied among regions. mRNA for the 444-amino acid-long variant, D2(444), was the most abundant form in pituitary and neostriatum. Intermediate levels of both D2(444) mRNA and the short form, D2(415), were detected in midbrain, and low levels of D2(444) and D2(415) mRNAs were detected in all other regions examined, including hippocampus, cerebellum, and cortex. The D2(444)/D2(415) ratio was generally lower in the regions of low expression than in pituitary and neostriatum. Dopamine-depleting lesions increased the density of D2 receptors in the denervated neostriatum by 29% without altering the affinity of the receptors for [3H]spiperone. The proliferation of receptors appeared to be due to a lesion-induced increase of up to 120% in the abundance of both variants of mRNA in the neostriatum.

PubMed Disclaimer

References

    1. Neuron. 1989 Aug;3(2):247-56 - PubMed
    1. Acta Physiol Scand Suppl. 1971;367:69-93 - PubMed
    1. Nature. 1988 Dec 22-29;336(6201):783-7 - PubMed
    1. Brain Res. 1985 Mar 11;329(1-2):225-31 - PubMed
    1. Brain Res. 1986 Dec;387(3):271-80 - PubMed

Publication types

MeSH terms

LinkOut - more resources