[Effects of Acupotomy Therapy on mRNA Expressions of Bcl-2, Bax, Caspase-3 in Posterior Cervical Extensor Muscles in Cervical Spondylosis Rabbits].

OBJECTIVE: To observe the effect of acupotomy therapy on mRNA expressions of Bcl-2, Bax , Caspase-3 in posterior cervical extensor muscles in cervical spondylosis rabbits, and explore its mechanisms for apoptosis of cervical muscles.

METHODS: New Zealand rabbits were randomly divided into normal, model, electroacupuncture (EA) and acupotomy groups, 6 in each group. The cervical spondylosis model was established by forced head-bowing for a long term. After model establishment, acupotomy was used at the trapezius muscle starting point and attachment site of sternocleidomastoid muscle, etc., once a week, total 3 times. EA was used at "Tianzhu" (BL 10), "Jingbailao" (EX-HN 15) and "Dazhu" (BL 11) for 3 weeks, 20 min a time, 3 times a week. Bcl-2, Bax, Caspase-3 mRNA expressions in posterior cervical extensor muscles were detected by real-time PCR.

RESULTS: There was no significant difference in the expression of Bcl-2 mRNA among all the groups ( P >0.05). Compared with the normal group, Bax mRNA increased in the model group ( P <0.01), and that in the acupotomy group was lower than that in the model group ( P <0.01). The ratio of Bcl-2/Bax mRNA in the model group decreased significantly compared with that in the normal group ( P <0.01); in comparison with the model group, the ratio in the acupotomy group increased ( P <0.01); and that in the acupotomy group was higher than the ratio in the EA group ( P <0.05). The Caspase-3 mRNA expression in the model group increased compared with that in the normal group ( P <0.05), and its expression in the acupotomy group decreased compared with those in the model and EA groups ( P <0.05).

CONCLUSIONS: Acupotomy therapy can regulate the mRNA expressions of Bax and Caspase-3, and retard apoptosis in posterior cervical extensor muscles, therefore the strained muscles are relieved, which may be one of its mechanisms for improving cervical spondylosis.