Metabolic brain disease · 2014
Antenatal taurine improves neuronal regeneration in fetal rats with intrauterine growth restriction by inhibiting the Rho-ROCK signal pathway.
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Liu Jing, Wang Hua-Wei, Liu Fang, Wang Xiao-Feng
Аннотация
The Rho-ROCK signal pathway is an important mediator of inhibitory signals that blocks central nervous cell regeneration. Here, we investigated whether antenatal taurine improved neuronal regeneration in fetal rats with intrauterine growth restriction (IUGR) by inhibiting this pathway. Thirty pregnant rats were randomly divided into three groups: control, IUGR, and IUGR + antenatal taurine supplementation (taurine group). The mRNA levels of Ras homolog gene A (Rho A), Rho-associated coiled-coil forming protein kinase 2 (ROCK2), and proliferating cell nuclear antigen (PCNA) were detected using real-time quantitative PCR. RhoA, ROCK2 and PCNA-positive cells were counted using immunohistochemistry. Antenatal taurine supplementation decreased RhoA and Rock2 mRNA expression, increased PCNA mRNA expression, and significantly decreased RhoA, ROCK2-positive and increased PCNA-positive cell counts in IUGR fetal rat brain tissues (p < 0.05). Thus, antenatal taurine supplementation inhibited the expression of key Rho-ROCK signal molecules and improved IUGR fetal brain development.
Предметные рубрики MeSH
AnimalsDose-Response Relationship, DrugDouble-Blind MethodDrug Evaluation, PreclinicalEnzyme InductionFemaleFetal Growth RetardationGene Expression Regulation, DevelopmentalMaleNerve RegenerationPregnancyProliferating Cell Nuclear AntigenRNA, MessengerRandom AllocationRatsRats, Sprague-DawleySignal TransductionTaurinerho-Associated KinasesrhoA GTP-Binding Protein