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刺激猫中脑导水管周围灰质对脊髓神经元对皮肤有害热刺激反应的抑制作用。

Inhibition of spinal neuronal responses to noxious skin heating by stimulation of mesencephalic periaqueductal gray in the cat.

作者信息

Carstens E, Yokota T, Zimmermann M

出版信息

J Neurophysiol. 1979 Mar;42(2):558-68. doi: 10.1152/jn.1979.42.2.558.

Abstract
  1. Discharges of lumbar dorsal horn neurons were evoked by noxious radiant skin heating, and inhibition of the heat-evoked responses by stimulation of the mesencephalic periaqueductal gray was investigated in N2O-anesthetized cats. 2. Thirty-seven units selected on the basis of receiving afferent C-fiber input from the posterior tibial and/or superficial peroneal nerves responded vigorously to 50 degrees C heating of the plantar surface of the ipsilateral hindpaw. All discharges were inhibited by periaqueductal gray stimulation (PAGS) at current strengths of 300--900 microA; the mean threshold for inhibition was 167 microamperemeter. The mean frequency of the inhibited discharge was 39% of the control response. 3. Effective PAGS sites were distributed throughout the ventral PAG bilaterally. Stimulus current-distance estimates indicate that small (0.5--1.2 mm diameter) volumes of tissue within the PAG were stimulated. 4. A monotonic relationship between temperature and unitary discharge was found for skin heating from threshold to about 50 degrees C. PAGS resulted in a decrease in the slope of the curve plotting discharge against temperature, without altering the threshold. 5. Inhibition of the heat-evoked discharges rarely outlasted the PAGS. 6. Possible neural substrates for descending inhibition and correlates with neural mechanisms of analgesia are discussed.
摘要
  1. 在氧化亚氮麻醉的猫中,通过对皮肤进行有害的辐射加热来诱发腰髓背角神经元的放电,并研究中脑导水管周围灰质刺激对热诱发反应的抑制作用。2. 根据从胫后神经和/或腓浅神经接受传入C纤维输入而选出的37个单位,对同侧后爪足底表面50℃的加热有强烈反应。所有放电在300 - 900微安的电流强度下均被导水管周围灰质刺激(PAGS)抑制;抑制的平均阈值为167微安/米。抑制后放电的平均频率为对照反应的39%。3. 有效的PAGS部位双侧分布于整个腹侧导水管周围灰质。刺激电流 - 距离估计表明刺激了导水管周围灰质内小(直径0.5 - 1.2毫米)体积的组织。4. 发现从阈值到约50℃的皮肤加热过程中,温度与单位放电之间存在单调关系。PAGS导致绘制放电与温度关系曲线的斜率降低,而不改变阈值。5. 热诱发放电的抑制很少超过PAGS。6. 讨论了下行抑制的可能神经基质以及与镇痛神经机制的相关性。

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