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Journal of Clinical Otorhinolaryngology Head and Neck Surgery ; (24): 415-422, 2011.
Article in Chinese | WPRIM | ID: wpr-748450

ABSTRACT

OBJECTIVE@#To study the mRNA expression of muscle phenotype and collagen of soft palate and pathology in obstructive sleep apnea hypopnea syndrome (OSAHS).@*METHOD@#We used the Real-time PCR to test the mRNA expression of soft palate muscle myosin heavy chain (MyHC) phenotype and collagen in 12 OSAHS patients and 8 control patients. We also distinguished the muscle isoforms I , II with ATPase staining, then counted the numbers of isoforms muscle fiber.@*RESULT@#The mRNA expression of OSAHS group was more than control group in II A MyHC phenotype (P<0.01). The number of OSAHS group muscle fibre I isoform was less than control group with pH4. 3 ATPase staining (P<0.05).@*CONCLUSION@#Compare to control group, the enhancement happened in the mRNA expression of II A MyHC phenotype which can increase the velocity and power but de crease the enduring quality of muscle in OSAHS, and the reduce be in the I MyHC isoform of muscle fiber that can cause muscle velocity become slower and persistency become longer in OSAHS patients.


Subject(s)
Female , Humans , Male , Middle Aged , Case-Control Studies , Muscle Fibers, Skeletal , Metabolism , Pathology , Myosin Heavy Chains , Metabolism , Palate, Soft , Metabolism , Pathology , Phenotype , Protein Isoforms , Metabolism , RNA, Messenger , Genetics , Sleep Apnea, Obstructive , Metabolism , Pathology
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