TY - JOUR
T1 - Repression of activity-dependent c-fos and brain-derived neurotrophic factor mRNA expression by pyrethroid insecticides accompanying a decrease in Ca2+ influx into neurons
AU - Imamura, Lisa
AU - Hasegawa, Hiroshi
AU - Kurashina, Kaori
AU - Hamanishi, Ayako
AU - Tabuchi, Akiko
AU - Tsuda, Masaaki
PY - 2000
Y1 - 2000
N2 - Permethrin, a type I pyrethroid insecticide, is known to affect sodium channels of neurons and prolong sodium currents. On the other hand, the expression of brain-derived neurotrophic factor (BDNF) and c-los genes is activated through Ca2+ influx into neurons, in an activity-dependent manner. In this study, therefore, we investigated whether permethrin influenced the Ca2+ signal-induced expression of these genes. In primary culture of mouse cerebellar granule cells (CGCs), stimulation with veratridine, a potent agonist for sodium channels, which causes membrane depolarization in neurons, induced c-fos and BDNF mRNA expression accompanying the Ca2+ influx into neurons. Pretreatment with permethrin at doses nontoxic to CGCs repressed the induction of these genes dose dependently, with trans-permethrin more potent than cis-permethrin. Consistent with this, the increase in Ca2+ influx caused by veratridine was repressed by permethrin. The membrane depolarization induced by elevating the potassium (K+) concentration in medium (high K+) caused the activation of c-fos and BDNF genes, which was also repressed by permethrin. Immunoblotting analysis of c-Fos and a gel-mobility assay of AP-1 DNA-binding activity supported the decrease in c-Fos synthesis in permethrin-treated CGCs. The type II pyrethroid cypermethrin also affected the expression of these genes but less effectively than permethrin. Thus, pyrethroids inhibit the activity-dependent gene expression in neurons.
AB - Permethrin, a type I pyrethroid insecticide, is known to affect sodium channels of neurons and prolong sodium currents. On the other hand, the expression of brain-derived neurotrophic factor (BDNF) and c-los genes is activated through Ca2+ influx into neurons, in an activity-dependent manner. In this study, therefore, we investigated whether permethrin influenced the Ca2+ signal-induced expression of these genes. In primary culture of mouse cerebellar granule cells (CGCs), stimulation with veratridine, a potent agonist for sodium channels, which causes membrane depolarization in neurons, induced c-fos and BDNF mRNA expression accompanying the Ca2+ influx into neurons. Pretreatment with permethrin at doses nontoxic to CGCs repressed the induction of these genes dose dependently, with trans-permethrin more potent than cis-permethrin. Consistent with this, the increase in Ca2+ influx caused by veratridine was repressed by permethrin. The membrane depolarization induced by elevating the potassium (K+) concentration in medium (high K+) caused the activation of c-fos and BDNF genes, which was also repressed by permethrin. Immunoblotting analysis of c-Fos and a gel-mobility assay of AP-1 DNA-binding activity supported the decrease in c-Fos synthesis in permethrin-treated CGCs. The type II pyrethroid cypermethrin also affected the expression of these genes but less effectively than permethrin. Thus, pyrethroids inhibit the activity-dependent gene expression in neurons.
UR - http://www.scopus.com/inward/record.url?scp=0033681008&partnerID=8YFLogxK
U2 - 10.1016/s0022-3565(24)39020-2
DO - 10.1016/s0022-3565(24)39020-2
M3 - 学術論文
C2 - 11082455
AN - SCOPUS:0033681008
SN - 0022-3565
VL - 295
SP - 1175
EP - 1182
JO - Journal of Pharmacology and Experimental Therapeutics
JF - Journal of Pharmacology and Experimental Therapeutics
IS - 3
ER -