Vendrell M, Tusell J M, Serratosa J
Dept. de Farmacologia i Toxicologia, CID-CSIC, Barcelona, Spain.
Neurotoxicology. 1992 Spring;13(1):301-8.
By means of in situ hybridization, the induction of proto-oncogene c-fos in rat brain after administration of several convulsants has been studied. The organochlorine insecticide gamma-hexachlorocyclohexane (lindane) has been shown to induce c-fos expression in a dose dependent manner. 30 mg/kg of lindane increased c-fos expression in cortical and hippocampal areas. The two non convulsant isomers of lindane, alpha- and delta-HCH, were not able to induce the expression of the proto-oncogene, but blocked that elicited by lindane. Pentylenetetrazole (PTZ) and picrotoxin (PTX), a known GABAA-receptor antagonist, have also been considered. Both of them were able to induce c-fos, although the pattern of expression was not the same in each case. alpha- and delta-HCH, were administered prior to the mentioned toxicants, affecting the proto-oncogene expression in different ways. We propose here that the distribution of c-fos mRNA after different treatments can be used as a marker of neurotoxic action.
通过原位杂交技术,研究了几种惊厥剂给药后大鼠脑中原癌基因c-fos的诱导情况。有机氯杀虫剂γ-六氯环己烷(林丹)已被证明以剂量依赖方式诱导c-fos表达。30mg/kg的林丹增加了皮质和海马区域的c-fos表达。林丹的两种非惊厥性异构体α-和δ-六氯环己烷不能诱导原癌基因的表达,但能阻断林丹引发的表达。还研究了已知的GABAA受体拮抗剂戊四氮(PTZ)和苦味毒(PTX)。它们都能够诱导c-fos,尽管每种情况下的表达模式不同。在上述毒物给药之前给予α-和δ-六氯环己烷,以不同方式影响原癌基因表达。我们在此提出,不同处理后c-fos mRNA的分布可作为神经毒性作用的标志物。