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
. 1989 Mar;14(3):271-7.
doi: 10.1007/BF00971323.

Glial uptake system of GABA distinct from that of taurine in the bullfrog sympathetic ganglia

Affiliations

Glial uptake system of GABA distinct from that of taurine in the bullfrog sympathetic ganglia

J Tasaka et al. Neurochem Res. 1989 Mar.

Abstract

The kinetics and specificity of GABA and taurine uptake were studied in the bullfrog sympathetic ganglia. GABA uptake system consisted of simple saturable component and taurine uptake system consisted of two saturable components exclusive of non-saturable influx. Taurine unaffected GABA uptake while GABA inhibited taurine uptake competitively with the Ki/Km ratio of 38. GABA (5.14 microM) uptake was inhibited by delta- aminovaleric acid and slightly by 2,4-diaminobutyric acid (5 mM, each) among ten structural analogs. Taurine uptake under high-affinity conditions was most strongly suppressed by hypotaurine and beta-alanine competitively with the Ki/Km ratio of 1.0 and 1.9, respectively. Autoradiography showed that glial cells were heavily labeled by both [3H]GABA and [3H]taurine. These results suggest that GABA is transported by a highly specific carrier system distinct from the taurine carrier and that taurine, hypotaurine, and beta-alanine may share the same high-affinity carrier system in the glial cells of the bullfrog sympathetic ganglia.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Neurochem Res. 1986 Feb;11(2):207-15 - PubMed
    1. Neurochem Res. 1979 Jun;4(3):339-54 - PubMed
    1. Neurochem Res. 1981 Nov;6(11):1179-91 - PubMed
    1. J Neurochem. 1987 Jun;48(6):1851-6 - PubMed
    1. Brain Res. 1986 Jan;389(1-2):63-75 - PubMed

MeSH terms