4.7 Article

Adiponectin regulates electroacupuncture-produced analgesic effects in association with a crosstalk between the peripheral circulation and the spinal cord

Journal

BRAIN BEHAVIOR AND IMMUNITY
Volume 99, Issue -, Pages 43-52

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbi.2021.09.010

Keywords

Adiponectin; AdipoR; AMPK; electroacupuncture; acupuncture analgesia; pain

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This study revealed a novel mechanism that acupuncture produces analgesic effects at least partially via the APN/AdipoR2-AMPK pathway in the spinal cord. The deletion of APN significantly reduced the acupuncture analgesia, while intrathecal administration of APN mimicked the analgesic effects of acupuncture. The study suggests that acupuncture may increase APN accumulation in the spinal cord through the blood circulation.
Neurotransmitter-mediated acupuncture analgesia has been widely studied in nervous systems. It remains largely unclear if peripheral substances are involved the acupuncture analgesia. Adiponectin (APN), a circulating adipokine, shows analgesic effects. The study aimed to examine whether APN regulates analgesic effects of electroacupuncture (EA) in the complete Freund's adjuvant (CFA)-induced mouse model. APN wild type (WT) and knockout (KO) mouse were employed in the study. We found that EA attenuates the CFA-induced pain as demonstrated by the Hargreaves thermal test and the von Frey filament test. The deletion of APN significantly reduced the acupuncture analgesia in the CFA-treated APN KO mice while the intrathecal administration of APN mimicked the analgesic effects of EA. We further revealed that EA produced analgesic effects mainly via APN/ AdipoR2-mediated AMPK pathway by the siRNA inhibitions of APN receptors (adipoR1/2) in the spinal cord. The immunofluorescence staining analysis showed that EA increased the APN accumulation in spinal cord through the blood circulation. In conclusion, the study indicates a novel mechanism that acupuncture produces analgesic effects at least partially via APN/AdipoR2-AMPK pathway in the spinal cord.

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