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The enhancement of glucose uptake caused by the collapse of gap junction communication is due to an increase in astrocyte proliferation
Author(s) -
Tabernero Arantxa,
Jiménez Cristina,
Velasco Ana,
Giaume Christian,
Medina José M.
Publication year - 2001
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.2001.00476.x
Subject(s) - gap junction , carbenoxolone , astrocyte , pentose phosphate pathway , tolbutamide , connexin , biology , glucose uptake , microbiology and biotechnology , biochemistry , chemistry , medicine , endocrinology , glycolysis , enzyme , insulin , intracellular , central nervous system
We have previously shown that several gap junction uncouplers increase the uptake of glucose in astrocytes. The aim of the present work was to study whether the increase in glucose uptake was a consequence of the inhibition of gap junction communication and the purpose of this effect. Our results show that α‐glycyrrhetinic acid and endothelin‐1 increase the uptake of glucose in highly, but not in poorly, coupled astrocytes. This effect depended on connexin 43 levels and was abolished when the inhibition of gap junction communication was prevented by tolbutamide or ouabain. The inhibition of gap junctions increased the rate of glucose incorporation into DNA and RNA, which was inhibited by treatment with dehydroepiandrosterone, an inhibitor of glucose‐6‐phosphate dehydrogenase, the regulatory enzyme of the pentose phosphate pathway. The inhibition of gap junctions significantly increased astrocyte proliferation, which was counteracted by tolbutamide. These effects were not observed in poorly coupled astrocytes expressing low levels of connexin 43. The increase in astrocyte proliferation caused by gap junction inhibition was prevented when either glucose uptake or the pentose phosphate pathway were inhibited. We conclude that the inhibition of gap junction communication induces astrocyte proliferation, resulting in an enhancement of glucose uptake and its utilization through the pentose phosphate pathway to provide ribose‐5‐phosphate for the synthesis of nucleic acids.