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KMID : 1034820080040020106
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Molecular & Cellular Toxicology
2008 Volume.4 No. 2 p.106 ~ p.112
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Nicotine Suppresses TNF- Expression in Human Fetal Astrocyte through the Modulation of Nuclear Factor- Activation
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Son Il-Hong
Park Yong-Hoon
Yang Hyun-Duk
Lee Sung-Ik
Han Sun-Jung
Lee Jai-Kyoo
Ha Dae-Ho
Kang Hyung-Won
Park Joo-Young
Lee Sung-Soo
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Abstract
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Parkinson’s disease (PD) progresses severely by a gradual loss of dopaminergic neurons in the substantia nigra (SN). Epidemiological studies showed that the incidences of PD were reduced by smoking of which the major component, nicotine might be neuroprotective. But the function of nicotine, which might suppress the incidences of PD, is still unknown. Fortunately, recently it was reported that a glial reaction and inflammatory processes might participate in a selective loss of dopaminergic neurons in the SN. The levels of tumour necrosis factor (TNF)- synthesised by astrocytes and microglia are elevated in striatum and cerebrospinal fluid (CSF) in PD. TNF- kills the cultured dopaminergic neurons through the apoptosis mechanism. TNF- release from glial cells may mediate progression of nigral degeneration in PD. Nicotine pretreatment considerably decreases microglial activation with significant reduction of TNF- mRNA expression and TNF- release induced by lipopholysaccharide (LPS) stimulation. Thus, this study was intended to explore the role of nicotine pretreatment to inhibit the expressions of TNF- mRNA in human fetal astrocytes (HFA) stimulated with IL-. The results are as follows: HFA were pretreated with 0.1, 1, and of nicotine and then stimulated with IL- (100 pg/mL) for 2h. The inhibitory effect of nicotine on expressions of TNF- mRNA in HFA with pretreated of nicotine was first noted at 8hr, and the inhibitory effect was maximal at 12 h. The inhibitory effect at of nicotine was inhibited maximal at 24 h. Cytotoxic effects of nicotine were noted above of nicotine. Moreover, Nicotine at 0.1, 1 and concentrations significantly inhibited IL--induced TF- activation. Collectively, these results indicate that in activated HFA, nicotine may inhibit the expression of TNF- mRNA through the pathway which suppresses the NF- activation. This study suggests that nicotine might be neuroprotective to dopaminergic neurons in the SN and reduce the incidences of PD.
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KEYWORD
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Nicotine, Tumor necrosis factor-, Astrocyte, NF-
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