Williams C A, Gopalan R, Nichols P L, Brien P L
Department of Physiology, College of Medicine, East Tennessee State University, Johnson City 37614-0576, USA.
Neuropeptides. 1995 Apr;28(4):209-18. doi: 10.1016/0143-4179(95)90024-1.
Antibody-coated microprobes were used to determine whether immunoreactive neurokinins (irNK) were released from sites in the brainstem during fatiguing isometric contractions of the triceps surae muscles in cats anesthetized with alpha-chloralose. Contractions were generated by stimulating the tibial nerve using a microprocessor-controlled stimulator. Microprobes were inserted into the periaqueductal grey (P 0.5-1.0 mm) or the medullary brainstem (either 3.0 or 3.5 mm rostral to the obex) prior to, during and following fatiguing contractions. No release of irNK was detected from the periaqueductal grey as a result of fatiguing isometric contractions. When probes were inserted 3.0 mm rostral to the obex, a basal release of irNK was detected from the medulla but this was inhibited during isometric contractions from sites corresponding to the lateral tegmental field. When probes were inserted into the more rostral site in the medulla (3.5 mm rostral to the obex), irNK were released in response to contractions from sites corresponding to lateral reticular nucleus, ventral regions of the nucleus tractus solitarius and the medial vestibular nucleus. No irNK were released from this site (3.5 mm rostral to obex) either during passive leg flexing, during nerve stimulation following gallamine injection and muscle paralysis or during stimulation of the central end of the cut tibial nerve. These results demonstrate that neurokinins are released from discrete sites in the medulla in response to fatiguing muscle contractions and suggest that tachykinin neurons may be a component of the pathways regulating blood pressure during ergoreceptor activation.
使用抗体包被的微探针来确定在用α-氯醛糖麻醉的猫中,在腓肠肌疲劳性等长收缩期间,免疫反应性神经激肽(irNK)是否从脑干中的位点释放。通过使用微处理器控制的刺激器刺激胫神经来产生收缩。在疲劳性收缩之前、期间和之后,将微探针插入导水管周围灰质(距表面0.5 - 1.0毫米)或延髓脑干(在闩前方3.0或3.5毫米处)。由于疲劳性等长收缩,未检测到导水管周围灰质中有irNK释放。当探针插入闩前方3.0毫米处时,检测到延髓有基础的irNK释放,但在对应于外侧被盖区的位点进行等长收缩期间,这种释放受到抑制。当探针插入延髓中更靠前的位点(闩前方3.5毫米处)时,对应于外侧网状核、孤束核腹侧区域和内侧前庭核的位点会因收缩而释放irNK。在被动腿部屈曲期间、加拉明注射和肌肉麻痹后的神经刺激期间或切断的胫神经中枢端刺激期间,该位点(闩前方3.5毫米处)均未释放irNK。这些结果表明,神经激肽会因疲劳性肌肉收缩而从延髓中的离散位点释放,并表明速激肽神经元可能是在工作感受器激活期间调节血压的通路的一个组成部分。