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Identification and characterization of pipecolic acid binding sites in mouse brain
Authors:Maria D. C. Gutierrez  Ezio Giacobini
Affiliation:(1) Department of Pharmacology, Southern Illinois University School of Medicine, P.O. Box 3926, 62708 Springfield, Illinois;(2) Present address: Laboratorio de Neuroquimica, Instituto Nacional de Neurologia y Neurocirujia, Insurgentes sur No. 3877, P.O. Box 3926, Mexico 2, D. F., Mexico
Abstract:Pipecolic acid (PA, piperidine-2-carboxylic acid) is the major product of lysine metabolism in the mammalian brain (Giacobini et al., 1980). In this study we have characterized the binding of [3H]PA to P2 fraction membranes and its distribution in the mouse brain. The binding was found to be saturable (70 nM), temperature and Na+ and Cl dependent. A high affinity binding site with an apparentKD of 33.2 nM and aBmax of 0.2 pmol/mg protein was demonstrated. The regional distribution of [3H]PA specific binding in mouse brain showed the highest concentration in cerebral cortex, thalamus and olfactory bulb. Unlabeled PA (10–3–10–11M) displaced specific binding of [3H]PA in a concentration dependent manner. Out of several substances tested, only proline showed a similar pattern of displacement. Pre-incubation of the membrane preparation with GABA (10–3–10–11M) resulted in either an increase or decrease of [3H]PA binding depending on the concentrations of GABA and PA. These results suggest a modulatory action of GABA on PA binding sites. The postnatal development of [3H]PA specific binding was studied in the whole brain of the mouse. [3H]Pipecolic acid binding increased progressively (8-fold) from one day after birth to 16 days. Following this developmental peak, the binding decreased gradually to 30 days at which age, adult values were attained.
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