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D-苯丙氨酸和丙谷胺对镇痛抑制系统的抑制作用。

Inhibition of the analgesia inhibitory system by D-phenylalanine and proglumide.

作者信息

Takeshige C, Mera H, Hisamitsu T, Tanaka M, Hishida F

机构信息

Department of Physiology, Showa University School of Medicine, Tokyo, Japan.

出版信息

Brain Res Bull. 1991 Mar;26(3):385-91. doi: 10.1016/0361-9230(91)90011-8.

Abstract

Stimulation of a nonacupuncture point (NAPS) does not normally produce analgesia in the same way that stimulation of an acupuncture point does. However, NAPS did produce dexamethasone reversible analgesia after intraperitoneal treatment with D-phenylalanine (DPA) or proglumide, or after microinjection of these compounds into such parts of the analgesia inhibitory system (AIS) as the lateral centromedian nucleus of the thalamus and part of the posterior hypothalamus. Inhibition of acupuncture analgesia (AA), or of morphine analgesia (MA) by 0.5 mg/kg, IP, which is equivalent to AA after AIS lesion, and of potentials in the lateral periaqueductal central gray evoked by repetitive NAPS or stimulation of the AIS, were antagonized by DPA. Disappearance of AA and MA in morphine tolerant acupuncture responder and nonresponder rats was reversed to reproduce the same magnitude of analgesia after proglumide application. The reproduced AA and MA were antagonized by dexamethasone. These results indicate that DPA and proglumide antagonized the AIS and unmasked the dexamethasone reversible AA and MA.

摘要

刺激非穴位通常不会像刺激穴位那样产生镇痛效果。然而,在用D-苯丙氨酸(DPA)或丙谷胺进行腹腔注射后,或者将这些化合物微量注射到镇痛抑制系统(AIS)的某些部位(如丘脑中央外侧核和下丘脑后部的一部分)后,非穴位刺激确实产生了地塞米松可逆性镇痛。腹腔注射0.5mg/kg可抑制针刺镇痛(AA)或吗啡镇痛(MA),这相当于AIS损伤后的AA,并且重复非穴位刺激或刺激AIS所诱发的导水管周围外侧中央灰质中的电位可被DPA拮抗。在吗啡耐受的针刺反应者和无反应者大鼠中,AA和MA消失,丙谷胺应用后可逆转以重现相同程度的镇痛。重现的AA和MA可被地塞米松拮抗。这些结果表明,DPA和丙谷胺拮抗了AIS并揭示了地塞米松可逆性AA和MA。

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