Li Jianhua, Mitchell Jere H
Moss Heart Center and Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9174, USA.
Am J Physiol Heart Circ Physiol. 2002 Sep;283(3):H1012-8. doi: 10.1152/ajpheart.00174.2002.
Static contraction of hindlimb skeletal muscle in cats induces a reflex pressor response. The superficial dorsal horn of the spinal cord is the major site of the first synapse of this reflex. In this study, static contraction of the triceps surae muscle was evoked by electrical stimulation of the tibial nerve for 2 min in anesthetized cats (stimulus parameters: two times motor threshold at 30 Hz, 0.025-ms duration). Ten stimulations were performed and 1-min rest was allowed between stimulations. Muscle contraction caused a maximal increase of 32 +/- 5 mmHg in mean arterial pressure (MAP), which was obtained from the first three contractions. Activated neurons in the superficial dorsal horn were identified by c-Fos protein. Distinct c-Fos expression was present in the L6-S1 level of the superficial dorsal horn ipsilateral to the contracting leg (88 +/- 14 labeled cells per section at L7), whereas only scattered c-Fos expression was observed in the contralateral superficial dorsal horn (9 +/- 2 labeled cells per section, P < 0.05 compared with ipsilateral section). A few c-Fos-labeled cells were found in control animals (12 +/- 5 labeled cells per section, P < 0.05 compared with stimulated cats). Furthermore, double-labeling methods demonstrated that c-Fos protein coexisted with nitric oxide (NO) synthase (NOS) positive staining in the superficial dorsal horn. Finally, an intrathecal injection of an inhibitor of NOS, N-nitro-L-arginine methyl ester (5 mM), resulted in fewer c-Fos-labeled cells (58 +/- 12 labeled cells per section) and a reduced maximal MAP response (20 +/- 3 mmHg, P < 0.05). These results suggest that the exercise pressor reflex induced by static contraction is mediated by activation of neurons in the superficial dorsal horn and that formation of NO in this region is involved in modulating the activated neurons and the pressor response to contraction.
猫后肢骨骼肌的静态收缩会引发反射性升压反应。脊髓浅背角是该反射首个突触的主要部位。在本研究中,通过电刺激麻醉猫的胫神经2分钟来诱发腓肠肌的静态收缩(刺激参数:30赫兹、持续时间0.025毫秒时为两倍运动阈值)。进行了十次刺激,每次刺激之间休息1分钟。肌肉收缩使平均动脉压(MAP)最大升高32±5毫米汞柱,这是从前三次收缩中获得的。通过c-Fos蛋白鉴定浅背角中被激活的神经元。在收缩腿同侧浅背角的L6-S1水平存在明显的c-Fos表达(L7水平每切片有88±14个标记细胞),而在对侧浅背角仅观察到散在的c-Fos表达(每切片9±2个标记细胞,与同侧切片相比P<0.05)。在对照动物中发现了一些c-Fos标记细胞(每切片12±5个标记细胞,与受刺激的猫相比P<0.05)。此外,双重标记方法表明c-Fos蛋白与浅背角中的一氧化氮(NO)合酶(NOS)阳性染色共存。最后,鞘内注射NOS抑制剂N-硝基-L-精氨酸甲酯(5毫摩尔)导致c-Fos标记细胞减少(每切片58±12个标记细胞),最大MAP反应降低(20±3毫米汞柱,P<0.05)。这些结果表明,静态收缩诱导的运动升压反射是由浅背角神经元的激活介导的,并且该区域中NO的形成参与调节被激活的神经元和对收缩的升压反应。