TY - JOUR
T1 - Melatonin, vitamin E, and estrogen reduce damage induced by kainic acid in the hippocampus
T2 - Potassium-stimulated GABA release
AU - Ortiz, Genaro G.
AU - Sánchez-Ruiz, Mayra Y.
AU - Tan, Dun Xian
AU - Reiter, Russel J.
AU - Benítez-King, Gloria
AU - Beas-Zárate, Carlos
PY - 2001
Y1 - 2001
N2 - Melatonin, vitamin E and estrogen have been shown to exert neuroprotective effects against kainic acid (KA)-induced damage in the hippocampus. The aim of the present study was to examine the changes in potassium-evoked γ-aminobutyric acid (GABA) release in the hippocampus of KA-treated rats and to test the possible protective effects of melatonin, vitamin E or estrogen. Following the treatment of mice with KA, a marked reduction in potassium-evoked [3H]GABA release was observed. Melatonin or estrogen prevented the reduction in potassium-evoked GABA release due to kainate administration. Vitamin E also exhibited some protective effect, but it was less than that provided by melatonin or estrogen. Melatonin, estrogen and, to a lesser extent, vitamin E reduce the physiological toxicity of KA. Since KA is believed to cause neuronal alterations via oxidative processes, it is assumed that the free radical scavenging and oxidative properties of melatonin, estrogen and vitamin E account for the protective effects of these agents.
AB - Melatonin, vitamin E and estrogen have been shown to exert neuroprotective effects against kainic acid (KA)-induced damage in the hippocampus. The aim of the present study was to examine the changes in potassium-evoked γ-aminobutyric acid (GABA) release in the hippocampus of KA-treated rats and to test the possible protective effects of melatonin, vitamin E or estrogen. Following the treatment of mice with KA, a marked reduction in potassium-evoked [3H]GABA release was observed. Melatonin or estrogen prevented the reduction in potassium-evoked GABA release due to kainate administration. Vitamin E also exhibited some protective effect, but it was less than that provided by melatonin or estrogen. Melatonin, estrogen and, to a lesser extent, vitamin E reduce the physiological toxicity of KA. Since KA is believed to cause neuronal alterations via oxidative processes, it is assumed that the free radical scavenging and oxidative properties of melatonin, estrogen and vitamin E account for the protective effects of these agents.
KW - Antioxidant
KW - Excitatory neurotransmitters
KW - Free radicals
KW - Glutamate
KW - Neuroprotection
KW - Reactive oxygen species
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U2 - 10.1034/j.1600-079X.2001.310109.x
DO - 10.1034/j.1600-079X.2001.310109.x
M3 - Article
C2 - 11485006
AN - SCOPUS:0034930202
SN - 0742-3098
VL - 31
SP - 62
EP - 67
JO - Journal of pineal research
JF - Journal of pineal research
IS - 1
ER -