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THE ROLE OF P_1-PURINERGIC RECEPTORS IN THE SPINAL MECHANISMS OF ACUPUNCTURE ANALGESIA
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作者 Liu Changning Zhao Feiyue Zhu Lixia Department of Physiology,Institute of Acupuncture and Moxibustion,China Academy of Traditional Chinese Medicine,Beijing 100700,China 《World Journal of Acupuncture-Moxibustion》 1993年第2期59-62,共4页
It has been extensively proved that electro-acupuncture elicit analgesia in bothextensive areas and local region via supraspinal structures and spinal cord.The present investigationwas to study the role of P<sub>... It has been extensively proved that electro-acupuncture elicit analgesia in bothextensive areas and local region via supraspinal structures and spinal cord.The present investigationwas to study the role of P<sub>1</sub>-purinergic receptors in the spinal mechanisms of weak electroacupuncture-induced analgesia.Leg withdrawal latency(LWL)to noxious radiant heat focused on the ankle regionwas used to assess the effects of acupuncture and that of P<sub>1</sub>-purinergic(adenosine)receptor antago-nists,theophylline and caffeine on the electro-acupuncture(EA)analgesia.EA prolonged the LWLby 16.7%±20.3%,with an after-effect lasting about 15 min.Both theophylline and caffeineblocked the EA-induced prolongation of LWL in a dose-dependent manner at the doses of 1.6-16 mg/kg.These results suggest that P<sub>1</sub>-purinegic receptor is involved in the spinal mechanisms of weak EAproduced analgesia in the rat. 展开更多
关键词 ELECTRO-ACUPUNCTURE ANALGESIA pl-purinergic receptor THEOPHYLLINE CAFFEINE
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