Pinching spine: A potential treatment for depression.

Author: Jiang LH, Wang LL, Wang MY, Wu HX, Zou YJ, Yuan XL, Chen MJ.
Affiliation:
Cultivating Candidate of the State Key Laboratory of Integrated Acupuncture and Medication, Nanjing University of Chinese Medicine, Nanjing, 210029, China, birddingdang@yahoo.com.cn.
Conference/Journal: Chin J Integr Med.
Date published: 2012 Mar 21
Other: Word Count: 231


OBJECTIVE:
To investigate whether pinching spine (PS, i.e., a traditional Chinese manipulative therapy) is benefificial to ameliorating the depressive state (including behavioral defificit, retardative weight gain and decreased sucrose consumption) in a rat model of depression induced by chronic unpredictable stress (CUS) and to explore the candidate mechanism of action.
METHODS:
PS was performed on rats' spine once daily for 1 week after exposure to CUS. The open-fifield test, body weight measuring, and sucrose intake test were applied on different dates: before stress (d0), at the end of stress (d21) and after PS treatment (d28), respectively. Then the rats' hippocampuses were performed genome-wide microarray analysis, and the expression levels of several genes were evaluated by real-time polymerase chain reaction (PCR).
RESULTS:
Exposure to CUS resulted in decreases of behavioral activity and sucrose consumption, which were reversed signifificantly after PS treatment. The expression of several genes relevant to energy metabolism, anti-oxidation, and olfactory receptor, etc., were down-regulated, while the expression of those relevant to hemostasis, immunity-inflammation, and restriction of activities and ingestion, etc., were up-regulated in hippocampuses of rats exposed to CUS. PS treatment signifificantly inverted these changes. Furthermore, increase or decrease in gene expression evaluated by realtime PCR was concordant with up-regulated or down-regulated expression evaluated by microarray analysis.
CONCLUSION:
PS showed a potential antidepressant-like effect, of which the action mechanism might be due to gene expression regulation in hippocampus.
PMID: 22438171

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