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pubmed-article:18404376pubmed:abstractTextThe Na(+)/H(+) exchanger has been the only unequivocally demonstrated H(+)-transport mechanism in the synaptosomal preparation. We had previously suggested that a Cl(-)-H(+) symporter (in its acidifying mode) is involved in cytosolic pH regulation in the synaptosomal preparation. Supporting this suggestion, we now show that: (1) when synaptosomes are transferred from PSS to either gluconate or sulfate solutions, the Fura-2 ratio remains stable instead of increasing as it does in 50 mM K solution. This indicates that these anions do not promote a plasma membrane depolarization. (2) Based in the recovery rate from the cytosolic alkalinization, the anionic selectivity of the Cl(-)-H(+) symporter is NO(3)(-) > Br(-) > Cl(-) >> I(-) = isethionate = sulfate = methanesulfonate = gluconate. (3) PCMB 10 muM inhibits the gluconate-dependent alkalinization by 30 +/- 6%. (4) Neither Niflumic acid, 9AC, Bumetanide nor CCCP inhibits the recovery from the cytosolic alkalinization.lld:pubmed
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pubmed-article:18404376pubmed:articleTitleAnionic selectivity sequence of the Cl(-)-H+ symporter in the synaptosomal preparation from rat brain cortex.lld:pubmed
pubmed-article:18404376pubmed:affiliationDepartamento de Fisiología y Farmacología, Facultad de Medicina, Universidad Autónoma de San Luis Potosi, Av. V. Carranza 2405, San Luis Potosi, S.L.P., 78210, Mexico.lld:pubmed
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