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1.
J Neurosci Res ; 99(11): 2874-2887, 2021 11.
Article in English | MEDLINE | ID: mdl-34510521

ABSTRACT

Axons in the adult mammalian central nervous system fail to regenerate after injury. By contrast, spontaneous axon regeneration occurs in the peripheral nervous system (PNS) due to a supportive PNS environment and an increase in the intrinsic growth potential induced by injury via cooperative activation of multifaceted biological pathways. This study compared axon regeneration and injury responses in C57BL/6 male and female mice after sciatic nerve crush (SNC) injury. The extent of axon regeneration in vivo was indistinguishable in male and female mice when observed at 3 days after SNC injury, and primary dorsal root ganglion (DRG) neurons from injured, male and female mice extended axons to a similar length. Moreover, the induction of selected regeneration-associated genes (RAGs), such as Atf3, Sprr1a, Gap43, Sox11, Jun, Gadd45a, and Smad1 were comparable in male and female DRGs when assessed by quantitative real-time reverse transcription polymerase chain reaction. Furthermore, the RNA-seq analysis of male and female DRGs revealed that differentially expressed genes (DEGs) in SNC groups compared to sham-operated groups included many common genes associated with neurite outgrowth. However, we also found that a large number of genes in the DEGs were sex dependent, implicating the involvement of distinct gene regulatory network in the two sexes following peripheral nerve injury. In conclusion, we found that male and female mice mounted a comparable axon regeneration response and many RAGs were commonly induced in response to SNC. However, given that many DEGs were sex-dependently expressed, future studies are needed to investigate whether they contribute to peripheral axon regeneration, and if so, to what extent.


Subject(s)
Peripheral Nerve Injuries , Animals , Axons/physiology , Female , Ganglia, Spinal/metabolism , Male , Mammals , Mice , Mice, Inbred C57BL , Nerve Regeneration/physiology , Peripheral Nerve Injuries/metabolism , Sciatic Nerve
2.
BMC Oral Health ; 14: 73, 2014 Jun 20.
Article in English | MEDLINE | ID: mdl-24950716

ABSTRACT

BACKGROUND: the aim of this study is to assess the association of harmful alcohol use based on the alcohol use disorders identification test (AUDIT) score with periodontal status according to gender and smoking in a representative sample of Korean adults. METHODS: This study analyzed 5,291 participants older than 19 years whose data of harmful alcohol use and periodontal status were available. Harmful alcohol use was defined by the WHO guidelines for the administration of AUDIT. The periodontal status was assessed by the Community Periodontal Index (CPI). Multivariate logistic regression analysis was performed with adjustment for socio-demographic variables, oral and general health behavior, oral health status and systemic conditions. All analyses considered a complex sampling design, and multivariate analysis was also performed in the subgroups. RESULTS: Multivariate logistic regression analysis revealed a marginal association between harmful alcohol use and higher CPI in the total sample. The adjusted odds ratio (OR) of harmful alcohol use was 1.16 (0.97 to 1.38) for higher CPI. Higher CPI was significantly associated with harmful alcohol use in men (OR: 1.28; 95% CI: 1.03-1.60) and non-smokers (OR: 1.29; 95% CI: 1.06-1.57). CONCLUSION: Periodontal status is significantly associated with harmful alcohol use in men and non-smokers in a representative sample of Korean adults.


Subject(s)
Alcohol Drinking/epidemiology , Periodontal Index , Smoking/epidemiology , Adult , DMF Index , Dental Devices, Home Care/statistics & numerical data , Diabetes Mellitus/epidemiology , Educational Status , Family , Female , Health Behavior , Health Status , Humans , Income/statistics & numerical data , Male , Obesity/epidemiology , Oral Health/statistics & numerical data , Periodontitis/epidemiology , Republic of Korea/epidemiology , Sex Factors , Toothbrushing/statistics & numerical data , Young Adult
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