耳针疗法与耳—迷走—内脏反射
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
针刺或按压耳穴调整内脏功能是临床常见的体表刺激疗法之一。支配外耳道和耳甲区的迷走神经耳支是迷走神经分布于周围皮肤的唯一分支,从发生学角度来看,来自鳃弓上基板到迷走神经节和其他神经节的走行关系不容忽略。而以往研究将耳针的作用机理归结为交感神经为主要传入途径的脊髓节段性调节,或者躯体传入与内脏传入在脑干整合的体表内脏联系,而忽视了耳甲区内脏神经的直接神经支配和与内脏中枢核团的直接联系。
     由于刺激迷走神经耳支引起了耳-心反射、耳-肺反射,类似于副交感紧张效应的临床的报道很多,如耵聍充塞耳道、耳内异物刺激或耳鼻喉科用耳窥镜,或冲洗耳道引起咳嗽,心率、血压下降,甚至心脏停搏。以往实验研究结果显示,针刺耳甲区引起大鼠血压下降、心率减慢,动脉推注阿托品后这种效应减弱或消失,说明刺激耳甲区激活了传出的副交感胆碱能神经纤维。
     经典解剖学认为,迷走神经耳支是迷走神经末梢在周围皮肤的分支,中枢走行中有舌咽神经和面神经加入,属于一般躯体神经,投射到三叉神经脊束核。体表刺激引起内脏效应通过脊髓水平中继,间接到达孤束核——公认的内脏传入的中继站,换元后发出纤维与内脏运动核团或网状结构联系,再次换元后到达所支配的内脏器官的神经节。本研究从电生理学和形态学两方面证实,刺激耳甲区可以激活迷走神经耳支直接投射到孤束核的一般内脏感觉传入纤维,通过与内脏运动核迷走神经背核联系激活迷走神经传出支配内脏的纤维,对内脏功能进行调节,确认耳-迷走神经-内脏反射的神经通路。由于副交感神经对心血管和胃肠支配效果相反,即抑制心脏而激活胃运动,因此本研究选用这两个系统,同时观察针刺耳甲区对副交感系统的激活效应。
     1 电生理实验:针刺耳甲区对大鼠孤束核、迷走神经背核神经元细胞外放电的影响及对心血管和胃运动的调节作用
     实验选用健康成年Sprague-Dawley雄性大鼠81只,体重300~350g之间,用10%的乌拉坦腹腔注射麻醉(urethane,1.0~1.2g/kg体重)。手术及实验动物体温用计算机温度时间控制仪维持在37℃左右。胃运动实验前禁食12小时,饲以5%葡萄糖盐水。
     记录到的自发或诱发孤束核和迷走神经背核神经元放电,选用对针刺双侧
Needling or pressing on auricular point is a common somato-stimulating therapy for treating visceral disorders. The auricular branch is the only peripheral branch of the vagus nerve. The fibers from the epibranchial placodes to the ganglia of the vagus and the course of vagus and other nerves have been observed in human being. However, in the previous studies the mechanism underlying the effects of auricular acupuncture on visceral function was conclusively attributed to the segmental innervations of sympathetic nervous system or the central integration between somatic and visceral input, omitting the direct visceral innervations of auricular concha.There were numerous clinic reports introducing parasympathetic excitation responses, such as cough, cardiac deceleration, even asystole and depression of blood pressure, induced by ear-cough-reflex and auriculo-cardiac-reflex following cerumen cramming in auditory canal, or stimulation of foreign body on ear, or speculum inspection, or douching ear canal. The previous study showed that acupuncture at auricular concha produced depressor and cardiac deceleration. After arterial atropine injection, the auricular acupuncture no longer inhibited the blood pressure and heart rate (HR)> indicating that the inhibitory effects were mediated by the excitation of parasympathetic nervous system after the stimulation of auricular concha.According to classical anatomy, the auricular branch of vagus is the branch innervating ear skin area, and its central projection affiliates glossopharyngeal nerve and facial nerve. This nerve belongs to somatic afferents and terminates in the nucleus of spinal tract of trigeminal nerve. Excitatory signals of somatic afferents producing visceral effect relay at spinal level and reach the nucleus of the tractus solitary (NTS) indirectly, a public relay station of visceral afferents. In NTS, the signals can be transmitted to other neurons projecting to visceral motor nuclei or reticular formation, which synapse with other neurons with efferent fibers innervating visceral ganglions. It was hypothesized in the present study that acupuncture at auricular concha might excite the auricular branch of vagus
    containing the primary visceral afferents projecting to NTS, and stimulate further the neurons in NTS and subsequently activate the motor nuclei of visceral such as the dorsal motor nucleus of vagus (DMV) so as to regulate the visceral function. Since the stimulation of parasympathetic nervous system can produce different effects on the cardiac system and gastrointestinal system, i.e. restraining the cardiac function and exciting the gastric movement, we investigated the function of the two systems simultaneously to detect the role of parasympathetic system in the mediation of the effects of auricular stimulation on the function of visceral organs.1 Electrophysiological experiment: The. influence of acupuncture at rats' auricular concha on the discharges of NTS and DMV neurons and on the cardiac and gastric functionThe male healthy Sprague-Dawley rats weighing 300-350g were anesthetized with 10% urethane (lgkg"1 i.p.) in the present study. During the operation and the whole experiment, the body temperature of the animals was kept at 37±1 °C by a Time Temperature Controller . The anminals were fed with 5% glucose saline during 12h fasting before the observation on gastric pressure.The extracellular discharge signals responding to the auricular stimulation were recorded with glass microelectrode and compared with those responding to the stimulation at the acupoints on body including ST36, S25 and P6. At the same time, mean arterial blood pressure (MAP), heart rate (HR) and gastric pressure (GP) were also recorded. Acupuncture was administered for 30s in all animals. After intravenous injection of atropine (0.18mg-kg"'), known to block cholinergic effect, the acupuncture stimulation was administered again to identify the involvement of vagus in the mediation of the effects of the auricular acupuncture.1.1 Results on intact ratsDuring 30 seconds of auricular acupuncture, the discharges of totally 363 NTS neurons in 71 rats were recorded. There were 222 neurons responding to acupuncture at ipsi-lateral auricular concha with a discharge increment of 3.50±0.32 spikes/sec which was 304.17±66.50% in percentage (PO.001); there were 159 neurons responding to acupuncture at contra-lateral auricular concha with a discharge increment of 3.45±0.56spikes/sec which was 415.73±103.36% in percentage (P<0.001); there were 100 neurons responding to acupuncture at ST36
    points with a discharge increment of 0.83±0.25 spikes/sec, i.e. 10.09±2.19% (P<0.01) in percentage; the discharge in 88 neurons responding to acupuncture at S25 points was increased by 0.60±0.20 spikes/sec, i.e. 10.77±2.64%(P<0.01) in percentage; the discharge in 81 neurons responding to acupuncture at P6 points was increased by 0.77±0.27 spikes/sec which is 12.90±2.77% in percentage (PO.01). There was no statistical significance between the effects produced by ipsi- and contra-lateral auricular stimulations on the discharge of NTS neurons (P>0.05), the effect of auricular acupuncture was significantly different from that produced by the acupuncture at the body acu-points (PO.001), indicating a better exciting effect of auricular acupuncture than that induced by the acupuncture at the body acu-points.During 30 seconds' acupuncture at 10 rats' auriculars, totally 40 DMV neurons were recorded, 36 of which responded to acupuncture at ipsi-lateral auricular concha with a discharge increment of 4.08±1.99 spikes/sec which was 100.43±28.63% in percentage (PO.05); 33 neurons responded to acupuncture at contra-lateral auricular concha with a discharge increment of 3.72±0.74 spikes/sec which was 112.91±31.13% in percentage (PO.001); 29 neurons responded to acupuncture at ST36 points with a discharge increment of 0.29±0.66 spikes/sec which was 10.84±5.87%in percentage (P>0.05); 20 neurons responded to acupuncture at S25 points with a discharge increment of 0.75±0.72 spikes/sec which was 20.63±7.50%in percentage (P>0.05); 20 neurons responded to acupuncture at P6 points with a discharge increment of 0.43±0.62 spikes/sec which was 22.76±10.72% in percentage (P>0.05). There was no statistical significance between the effects produced by ipsi- and contra-lateral auricular stimulations on the discharge of DMV neurons (P>0.05), the effect of auricular acupuncture was significantly different from that produced by the acupuncture at the body acu-points (.P<0.05), indicating a better exciting effect of auricular acupuncture than that induced by the acupuncture at the body acu-points.During 30 seconds' acupuncture at ipsi-lateral auricular concha in 30 rats, the HR responded with a reduction of 15.60±3.11 beats/sec which was 3.70±0.75% in percentage CP<0.001); when acupuncture at contra-lateral auricular concha in 32 rats, the HR responded with a reduction of 11.63±2.19 beats/sec which was 2.70±0.48% in percentage (PO.001); when acupuncture at ST36 in 31 rats, the HR responded with a increment of 3.87±1.29 beats/sec which was 0.94±0.32% in
    percentage (PO.01); when acupuncture at S25 in 27 rats, the HR responded with a increment of 4.44±2.04 beats/sec which was 1.12±0.51% in percentage (PO.05); when acupuncture at P6 in 30 rats, the HR responded with a increment of 1.20 ± 1.45 beats/sec which was 0.27±0.37% in percentage (P>0.05). There was no statistical significance between the effects produced by ipsi-and contra-lateral auricular concha stimulations on HR (P>0.05), the effect of auricular acupuncture was significantly different from that produced by the acupuncture at body acu-points (PO.01), indicating acupuncture at auricular had decrease effect but acupuncture at body acu-points had no or increase effect on HR.During 30 seconds' acupuncture at ipsi-lateral auricular concha in 29 rats, the MAP responded with a reduction of 12.10±1.05 mmHg which was 11.89±1.11% in percentage (PO.001); when acupuncture at contra-lateral auricular concha in 29 rats, the MAP responded with a reduction of 9.89±1.44 mmHg which wasl0.00±1.35% in percentage (PO.001); when acupuncture at ST36 in 27 rats, the MAP responded with a increment of 2.08±1.29 mmHg which was 1.35±1.40% in percentage (P>0.05); when acupuncture at S25 in 27 rats, the MAP responded with a reduction of 6.35±1.32 mmHg which was 6.28±1.38% in percentage (PO.001); when acupuncture at P6 in 27 rats, the MAP responded with a reduction of 2.07±1.07 mmHg which was 1.89±L09% in percentage (P>0.05). There was no statistical significance between the depressor effects produced by ipsi-and contra-lateral auricular concha stimulations on MAP (P>0.05), and the effect of ipsi-auricular acupuncture was significantly different from that produced by the acupuncture at body acu-points (PO.05), and the depressor effect of S25 was similar to that of contra-lateral aucicular, both of them had better depressor effect than ST36 and P6 (PO.05).During 30 seconds' acupuncture at ipsi-lateral auricular concha in 14 rats, the GP responded with a increment of 17.35±3.26 mmH20 which was 17.28±6.39% in percentage (PO.001); when acupuncture at contra-lateral auricular concha in 15 rats, the GP responded with a increment of 19.28±3.77 mmH20 which wasl8.73±5.37% in percentage (PO.001); when acupuncture at ST36 in 18 rats, the GP responded with a increment of 1O.H±1.86 mmH20 which was 10.20±2.54% in percentage (P<0.001); when acupuncture at S25 in 18 rats, the GP responded with a reduction of 15.88±3.75 mmH20 which was 10.50±2.45% in percentage (P<0.001);
    when acupuncture at P6 in 18 rats, the GP responded with a increment of 11.42±1.76 mmH2O which was 8.31±1.87% in percentage (PO.001). There was no statistical significance among the effects produced by acupuncture at ipsi- auricular concha, contra-lateral auricular concha, ST36 and P6 stimulations on GP (P>0.05), but all of them had different effect on GP with acupuncture at S25, which had inverse effect on GP(PO.OOl).1.2 Results on atropine-treated ratsAfter intravenous administration of atropine in 34 rats the discharges in 22 NTS neurons responding to acupuncture at ipsi-lateral auricular concha and contra-lateral auricular concha were increased by 3.58±0.82 spikes/sec and 3.44±0.76 spikes/sec, corresponding to the percentages of 61.82±12.04% (PO.OOl) and 75.24±19.26% (PO.001) respectively. The discharges in 20 NTS neurons responding to acupuncture at ST36 points and 24 NTS neurons responding to acupuncture at S25 points were increased by 1.51 ±0.43 spikes/sec and 1.40±0.43 spikes/sec, equal to a percentage of 26.03±6.44%(P<0.01) and 26.26±6.52% (P<0.01) separately; in 24 neurons responding to acupuncture at P6 points the discharges were increased by 1.40±0.44 spikes/sec , a percentage of 28.10±6.18% (PO.01). Compare effect of acupuncture at auricular concha and body points on the NTS extracellular discharges after atropine, there was no statistical significance between ipsi- and contra-lateral auricular (P>0.05) stimulation, but there did exist differences between both auricular and other body points (P<0.05), by and large, indicating a better exciting effect of auricular than of body points after atropine injection. Compare the excitation effect of the same stimulation site pre- and post-atropine, there was no statistical difference all the points (P>0.05). There was no statistical difference in the excitatory effects induced by every acupoint stimulated before and after administration of atropine.After intravenous administration of atropine, the HR was recorded in some animals. After acupuncture at ipsi-lateral auricular concha in 30 rats, the increment of HR was 2.80 ± 2.05 beats/sec, a percentage of 0.65 ± 0.51% (P>0.05); acupuncture at contra-lateral auricular concha on 32 rats, the increment of HR was 3.75 ± 2.31 beats/sec, a percentage of 0.79 ± 0.51% (P>0.05); acupuncture at ST36 on 31 rats, the increment of HR was 4.65 ± 1.07 beats/sec, a percentage of 1.07 ± 0.24% (?<0.001); acupuncture at S25 on 27 rats, the increment of HR was 3.11 ±
    1.76 beats/sec, a percentage of 0.69 ± 0.40% (P>0.05); acupuncture at P6 on 30 rats, the increment of HR was 3.20 ± 1.40 beats/sec, a percentage of 0.73 ±0.31% (P<0.05). Compare the effect of acupuncture at auricular concha and body points on HR, there was no statistical significance among all the groups (P>0.05). Compare the influence of the same stimulation site pre- and post-atropine, there existed apparent statistical difference in both auricular stimulation groups (PO.01) for contrary responsive direction; ST36 and S25 had similar effect pre- and post-atropine injection (P>0.05); acupuncture at P6 had a small increase effect on HR after atropine CP<0.05).After intravenous administration of atropine, the MAP was recorded on some animals. Acupuncture at ipsi-lateral auricular concha on 29 rats, the reduction of MAP was 3.84 ± 0.90 mmHg, a percentage of 4.80 ± 1.11% (PO.001); acupuncture at contra-lateral auricular concha on 29 rats, the reduction of MAP was 3.28 ± 0.91 mmHg (PO.01), a percentage of 4.23 ± 1.17%; acupuncture at ST36 on 27 rats, the reduction of MAP was 1.69 ± 0.80 mmHg, a percentage of 2.07 ± 1.00%(PO.05); acupuncture at S25 on 27 rats, the reduction of MAP was 1.75 ±0.97 mmHg, a percentage of 5.83 ± 1.08 (PO.001); acupuncture at P6 on 27 rats, the reduction of MAP was 1.75 ± 0.97mmHg, a percentage of 2.21 ± 1.33% (P>0.05). Compare the depressor effect of acupuncture at auricular concha and body points after atropine, there was no statistical difference on depressor effect among all the points except S20, which still had better depressor effect than the other two points (PO.05). Compare the depressor effect of the same stimulation site pre- and post-atropine, there existed apparent statistical difference in both auricular stimulation groups (PO.001) and S20 points (PO.05).After intravenous administration of atropine, the GP was recorded on some animals. Acupuncture at ipsi-lateral auricular concha on 14 rats, the increment of GP was 1.01 ± 1.21 mmH20, a percentage of 0.52 ± 1.89% (P>0.05); acupuncture at contra-lateral auricular concha on 15 rats, the increment of GP was 2.78 ± 1.75 mmH20, a percentage of 4.72 ± 1.75% (P>0.05); acupuncture at ST36 on 18 rats, the increment of GP was 2.09 ± 1.01 mmH20, a percentage of 1.51 ± 2.30% (P>0.01); acupuncture at S2s on 18 rats, the increment of GP was 0.00 ± 1.05 mmH20, a percentage of 1.09 ± 1.07% (P>0.05); acupuncture at P6 on 18 rats, the increment of GP was 0.50 ± 2.01 mmH20 , a percentage of 0.24 ± 2.87% (P>0.05). There was no
    statistical significance among all the groups after atropine (P>0.05). There existed statistical difference in all groups (PO.05) pre- and post- atropine injection.2 Morphological experiment: research the direct projection from auricular concha to NTS by neuronal tracing technology and immunohistochemistry methodsThe male healthy Sprague-Dawley rats weighing 200-250 g were anesthetized with 10% urethane (1.0~1.2gkg"' i.p.). 20% PBS solution of biocytin and 4% PBS solution of Pseudorabies Virus (PrV) were subcutaneously injected into rats' auricular concha and external auditory canal opening from 3-4 separate points. The medulla oblongata and interbrain were removed rapidly under anesthesia with 10% urethane 72 hours after injection of biocytin and PrV and cut into 20|i slices. The brain slices were detected by immunohistochemistry methods.In addition, the Fos-protein expressed in NTS of the rats was also determined with immunohistochemistry methods after the stimulation of electroacupuncture at auricular concha for 30 minutes. The results are as follows.2.1 Result after injection of biocytin as a neuronal pathway tracerSparsely labeled fibers were found from rostral to obex in NTS. And comparatively more labeled fibers were exhibited in the nucleus of spinal tract of trigeminal nerve, postrema and reticular formation.2.2 Result after injection of PrV as a neuronal pathway tracerThe labeled neurons appeared in NTS, DMV, the nucleus of spinal tract of trigeminal nerve and the nucleus of ambiguous. In NTS the labeled neurons mainly scattered from rostral to obex.2.3 c-fos protooncogene expression in oblongata after electro-acupuncture stimulation on auricular concha of ratsFos protein stained neurons were spread along whole NTS, but more labeled neurons appeared from rostral to the opening base of the four ventricle. Quite more expressions were found in DMV, and densely labeled neurons existed in the bilateral nucleus of spinal tract of trigeminal nerve and reticular formation of medulla oblongata.
引文
1 Bourdiol R.耳针疗法.周一方译自《生物疗法讲座》(法文)33期副本1972,PP.1-22.
    2 Nogier P. Deutsche Zeitschrift fuer Akupunctur. 1957;6(3~4):25.
    3 Tblkouuheka R.eA. OcHo BbINrpope'nekcu Tepan Nm. 1979; p.287.
    4 Cho MH,Nogier P.医道日本,1978;(11):16.
    5 中华人民共和国国家标准—耳穴名称与部位(GB-T 13734-92),北京:国家标准出版社 1993年版。
    6 Mitchell, G.A.G. The autonomic nerve supply of the throat, nose and ear, J. Laryngol. Otol. 1953; 68: 495-516.
    7 Hunt Jr. The sensory field of the facial nerve: A further contribution to the symptomatology of the eniculate ganglion. Brain. 1915; 38: 418.
    8 Hollinshead WH. Anatomy for Surgeons: Ⅰ, The Head-Neck. New York, Harper and Row, 1968, pp.190-191.
    9 Hollinshead WH. Anatomy for Surgeons: The Head-Neck, 3rd editon. New York, Harper and Row, 1982, pp. 162.
    10 Guild SR. The glomus jugulare, a non chromaffin paraganglion in man. Ann Otol Rhinol Laryngol. 1953;62(4):1045-1071.
    11 Tekdemir I, Aslan A, Elhan A. A clinico-anatomic study of the auricular branch of the vagus nerve and Arnold's ear-cough reflex. Surg Radiol Anat. 1998; 20(4): 253-257.
    12 张诗兴,周坤福,姜文方等.耳穴的脑、脊神经节投射.上海针灸杂志.2002;21(3):35-36.
    13 Barr ML, Kiernan JA. The Human Nervous System. An anatomical view point, 4th edition, Philadelphia. Harper and Row, 1983; pp.138.
    14 Williams PL, Warwick R in: Gray's Anatomy, 36th edition, 1980, Churchill-Livingstone, Edinburgh, London. pp. 1079-1081.
    15 中国科学院动物研究所.猫耳廓的神经分布.针刺麻醉原理的探讨.北京:人民卫生出版社 1974年版.pp.37-40.
    16 中国科学院动物研究所.人耳廓及其穴位里的神经分布.针刺麻醉原理的探讨.北京:人民卫生出版社 1974年版.pp.41-46.
    17 张启兵.耳针作用的形态学机理研究.上海针灸杂志.2003;22(1):46-47.
    18 Jean A. The nucleus tractus solitarius: neuroanatomic, neurochemical and functional aspects. Arch Int Physiol Biochim Biophys. 1991; 99(5): A3-52.
    19 Zhang LL, Ashwell KW. The development of cranial nerve and visceral afferents to the nucleus of the solitary tract in the rat.Anat Embryol (Berl). 2001; 204(2): 135-151.
    20 Kalia M, Mesulam MM. Brain stem projections of sensory and motor components of the vagus complex in the cat: I. The cervical vagus and nodose ganglion. J Comp Neurol. 1980; 193(2): 435-465.
    21 Kalia M, Mesulam MM, Mesulam. Brain stem projections of sensory and motor components of the vagus complex in the cat: II. Laryngeal, tracheobronchial, pulmonary, cardiac, and gastrointestinal branches. J Comp Neurol. 1980; 193(2): 467-508.
    22 Estes ML, Block CH, Barnes KL. The canine nucleus tractus solitarii: light microscopic analysis of subnuclear divisions. Brain Res Bull. 1989; 23(6): 509-517.
    23 Loewy AD, Burton H. Nuclei of the solitary tract: efferent projections to the lower brain stem and spinal cord of the cat. J Comp Neurol. 1978; 181(2): 421-449.
    24 Kalia M, Sullivan JM. Brainstem projection of sensory and motor components of the vagus nerve in the rat. J. Comp Neurol. 1982; 211(3): 248-265.
    25 Hyde TM, Miselis RR. Subnuclear organization of the human caudal nucleus of the solitary tract. Brain Res Bull. 1992; 29(1): 95-109.
    26 Berk ML. Projections of the lateral hypothalamus and bed nucleus of the stria teminalis to the dorsal vagal complex in the pigeon. J Comp. Neurol. 1987; 260 (1): 140-156.
    27 Gray TS, Magnuso DJ. Neuropeptide neuroonal efferents from the bed nucleus of the stria-terminalis and central amgydaloid nucleus to the dorsal vagal complex in the rat. J Comp Neurol. 1987; 262(3): 365-374.
    28 Okuma Y, Osumi Y. Central cholinergic descending pathway to the dorsal motor nucleus of the vagus in the regulation of gastric function. J Pharmacol. 1986; 41(3): 373-379.
    29 Kalia M, and Richter D. Morphology of identified slowly adapting lung strech receptor afferents stained with intra-axonal horseradish peroxidase in the tractus solitarius of the cat. I. A light microscopic analysis. J Comp Neurol. 1985; 241 (4): 503-520.
    30 Gwyn DG, Leslie RA, Hopkins DA. Observations on the afferent and efferent organization of the vagus nerve and the innervation of the stomach in the squirrel monkey. J Comp Neurol. 1985; 239(2): 163-175.
    31 Massari VJ, Shirahata M, Johnson TA, Gatti PJ. Carotid sinus nerve terminals which are tyrosine hydroxylase immunoreactive are found in the commissural nucleus of the tractus solitarius. J Neurocytol. 1996; 25 (3): 197-208.
    32 Menetrey D, Basbaum AI. Spinal and trigeminal projections to the mucleus of the solitary tract: a possible substrate for somatovisceral and viscerovisceral reflexes activation. J. Comp. Neurol. 1987; 255(3): 439-450.
    33 Norgren R. Projections from the nucleus of the solitary tract in the rat. Neurosci. 1978; 3(2): 207-218.
    34 Boscan P, Pickering AE, Paton JF. The nucleus of the solitary tract: an integrating station for nociceptive and cardiorespiratory afferents.Exp Physiol. 2002; 87(2):259-266.
    35 Nomura S, Mizuno N. Central distribution of primary afferent fibers in the Arnold's nerve(the auricular branch of the vagus nerve): a transganglionic HRP study in the cat. Brain Res. 1984; 292(2): 199-205.
    36 Gwyn DG, Leslie RA, Hopkins DA. Gastric afferents to the nucleus of the solitary tract in the cat. Neurosci. Lett., 1979; 14(1): 13-17.
    37 Leslie RA, Gwyn DG and Hopkins, D. A., The central distribution of the cervical vagus nerve and gastric afferent and efferent projections in the rat. Brain Res. Bull. 1892; 8(1): 37-44.
    38 Roger RC, Hermann GE. Central connection of the hepatic branch of the vagus nerve: a horseradish peroxidase histochemical study. J Auton Nerv Syst. 1983; 7(2): 165-174.
    39 Satomi H, Takahashi K. Distribution of the cells of primary afferent fibers to the cat auricle in relation to the innervated region. Anat Anz. 1991; 173(2): 107-112.
    40 Folan-Curran J, Hickey K, Monkhouse WS. Innervation of the rat external auditory meatus: a retrograde tracing study. Somatosens Mot Res. 1994; 11(1):65-68.
    41 Keller JT, Beduk A, Saunders MC. Central brainstem projections of the superior vagal ganglion of the cat. Neurosci Lett. 1987; 75(3): 265-270.
    42 Liu D, Hu Y. The central projections of the great auricular nerve primary afferent fibers—an HRP transganglionic tracing method. Brain Res. 1988; 445(2): 205-210.
    43 Bengoechea O, Insausti R, Gonzalo LM. Spinal topography of the projection of the auricular nerve in the rabbit: a transganglionic WGA-HRP study. Brain Res. 1985; 329(1-2): 340-345.
    44 江苏新医学院第二附院.耳麻取穴与内脏神经的关系.针刺麻醉原理的探讨.北京:人民卫生出版社 1974年版.pp.364-366.
    45 Chien CH, Shieh JY, Ling EA, et al. The composition and central projections of the internal auricular nerves of the dog. J Anat. 1996; 189 (Pt 2):349-362.
    46 Campbell R, Rodrigo D, Cheung L. Asystole and bradycardia during maxillofacial surgery. Anesth Prog. 1994; 41(1): 13-16.
    47 Mantle-St John LA, Tracey DJ. Somatosensory nuclei in the brainstem of the rat: independent projections to the thalamus and cerebellum. J Comp Neurol. 1987; 255(2): 259-271.
    48 Gamboa-Esteves FO, Lima D, Batten TF. Neurochemistry of superficial spinal neurones projecting to nucleus of the solitary tract that express c-fos on chemical somatic and visceral nociceptive input in the rat. Metab Brain Dis. 2001; 16(3-4): 151-164.
    49 Meng Z, Lu G. Projection linkage from spinal neurons to both lateral cervical nucleus and solitary tract nucleus in the cat. Biol Signals Recept. 2000; 9(1): 38-44.
    50 Engel D. The gastroauricular phenomenon and related vagus reflexes. Arch Psychiatr Nervenkr. 1979; 227(3): 271-277.
    51 Engel D. Uber das reflektorische Ohrenjucken bei Sodbrennen. Med. Klin. 1922; 47: 1495-1497.
    52 Malherbe, W.D.F. Otalgia with oesophageal hiatus hernia. Lancet 1958 Ⅰ, 1368-1369.
    53 Deutsch, M. Ein Beitrag zur Symptomatomatologie der beginnenden Lungentuberkulose. Med. Klin. 1919; 43: 1090-1091.
    54 Bradford, F K. The auriculo-genital reflex in cats. J Exp Physiol. 1937; 27:272-279.
    55 Vasiliu, D.I. Reflex auriculo-uterin. Spitalul. 1932; 52: 396.
    56 Aschner. In: The neurological examination, De Jong, R.N. (ed.), Hober Med. Division. New York, London, 1967.p.315.
    57 Kalchschmidt, In: Lehrbuch der klinischen Diagnostik, J.mared, J. Mosci (eds),. Jena: G. Fischer, 1956. pp.293-294.
    58 Berlin, R. Theagstro-auricular phenomenon. Lancet 1959 Ⅰ, pp.734-735.
    59 Beer, G. R. de, Vertebrate zoology. London: Sidgwick and Jackson. 1936.
    60 Arey L. B. Developmental anatomy. Philadelphia: W.b.Saunders. 1961.
    61 Faber, K. Reflexhyperasthesien bei Verdauungskrankheiten. Dtsch. Arch. Klin. Med. 1990; (65), 332-384.
    62 Todisco T. The oto-respiratory reflex. Respiration. 1982; 43(5): 354-358.
    63 Clay L. Cough as a symptom. Med Clin North Am. 1947; 31:1393-1399.
    64 Wolff AP, May M, Nuelle D. The tympanic membrane, source of the couth reflex. JAMA. 1973; 223(11): 1296.
    65 May KL. Arnold's nerve reflex among pollinosis patients: sign of predictable asthma? J Investig Allergol Clin Immunol. 1996; 6(1): 47-49.
    66 Head H. On disturbances of sensation with special reference to pain of visceral disease. Brain. 1894; 17:339-480.
    67 钱志益.酒精药面塞耳可治通经、头痛、头晕.大众医学.1983:5:36.
    68 Aschner B. Uber einen bisher noch nicht beschriebenen Reflex von Auge auf Krieslauf und Atmung: Verschinden des Radialispulses bei Druk auf das Auge. Wein Klin Wschr. 1908; 21: 1529-1530.
    69 Dagnini G. Intorno ad un riflesso provocato in alcuni emiplegici collo stimolo della cornea e colla pressione sul bulbo oculare. Boll Sci Med. 1908; 8: 380-381.
    70 Salamagne JC. Le reflexe oculo-cardiaque L' anesthesia en Ophtalmologie-ⅩⅩⅦ Congres National d' Anesthesie et de Reanimation, Bordeaux France, 1979. pp.41-59.
    71 Anderson RL. The blepharocardiac reflex. Arch Ophthal. 1978; 96(8):1418-1420.
    72 Kwik RS. Marcus Gunn syndrome associated with an unusual oculo-cardiac reflex. Anaesthesia. 1980; 35(1): 46-49.
    73 Yamashita M. Oculocardiac reflex and the anesthesiologist. Middle East J Anesthesiol. 1986; 8(5): 399-415.
    74 Apt L, Isenberg S, Gaffney WL. The oculocardiac reflex in strabismus surgery. Am J Ophthamol. 1973; 76(4): 533-536.
    75 Welhar W, Johnson D. The oculocardiac reflex during extraocular muscle surgery. Arch Ophthalmol. 1965; 73: 43.
    76 Mosomworth P, Ziegler Z, Jacob J. The oculocardiac reflex in eye muscle surgery. Anesthesiology. 1958; 19: 7.
    77 Hayes RW, McBrearty E. An oculo-cardiac hypothesis of sudden unexpected death in infants. Med Hypotheses. 1979; 5(4): 477-80.
    78 Gandevia SC, McCloskey DI, Potter EK. Reflex bradycardia occurring in response to diving, nasopharyngeal stimulation and ocular pressure, and its modification by respiration and swallowing. J Physiol. 1978; 276: 383-394.
    79 Alexander JP. Reflex disturbances of cardiac rhythm during ophthalmic surgery. Br J Ophthalmol. 1975; 59(9): 518-524.
    80 Arnold RW, Gould AB, MacKenzie R, Dyer JA, Low PA. Lack of global vagal propensity in patients with oculocardiac reflex. Ophthalmology. 1994; 101(8): 1347-52.
    81 Lynch MJ, Parker H. Forensic aspects of ocular injury. Am J Forensic Med Pathol. 2000 Jun; 21(2): 124-6.
    82 Kaufman L. Cardia arrhythmias in dentistry. Lancet. 1965; 1: 27.
    83 Kaufman L. Unforseen complications encountered during dental anaesthesia. Proc R Soc Med.1966; 59(8): 731-734.
    84 Cha ST, Eby JB, Katzen JT, et al. Trigeminocardiac reflex: a unique case of recurrent asystole during bilateral trigeminal sensory root rhizotomy. J Craniomaxillofac Surg. 2002; 30(2): 108-111.
    85 Kratschmer F. Uber Reflexe von der Nasenschleimhaut auf Athmung und Kreislauf. SberAkad Wis Wien .1870; 62: 147-170.
    86 Angell-James JE, Daly MB. Nasal reflexes. Proc Roy Soc Med. 1969; 62(12): 1287-1293
    87 Angell-James JE, Daly MB. Some aspects of upper respiratory tract reflexes. Acta Otolaryngol. 1975; 79(3-4): 242-252.
    88 Blanc VF. Trigeminocardiac reflexes. Can J Anaesth. 1991; 38(6): 696-699.
    89 Robideaux V. Oculocardiac reflex caused by midface disimpaction. Anesthesiology. 1978;49(6): 433.
    90 Bainton R, Lizi E. Cardiac asystole complicating zygomatic arch fracture. Oral Surg Oral Med Oral Pathol. 1987; 64(1): 24-25.
    91 Loewinger J, Cohen M, Levi E. Bradycardia during elevation of a zygomatic arch fracture. J Oral Maxillofac Surg. 1987; 45(8): 710-711.
    92 Shearer ES, Wenstone R. Bradycardia during elevation of zygomatic fractures. A variation of the oculocardiac reflex. Anaesthesia 1987; 42(11):1207-1208.
    93 Shelly MP, Church JJ. Bradycardia and facial surgery (letter). Anaesthesia. 1988; 43:422.
    94 Hopkins CS. Bradycardia during nerosurgery- a anew reflex? (Letter). Anaesthesia. 1988; 43(2): 57-158.
    95 Stott DG. Reflex bradycardia in facial surgery. Br J Plast Surg. 1989; 42(5):595-597.
    96 Ragno JR, Marcoot RM, Taylor SE. Asystole during Le Fort I osteotomy. J Oral Maxillofac Sug.1989; 47(10): 1082-1083.
    97 Bainton R, Barnard N, Wiles JR, et al. Sinus arrest complicating a bitemporal approach to the treatment of pan-facial fractures. Br J Oral Maxillofac Surg.1990; 28(2): 109-110.
    98 Lang S, Lanigan DT, van der wal M. trigeminocardiac reflexes: maxillary and mandibular variants of the oculocaridac reflex. Can J Anaesth. 1991; 38(6): 757-760.
    99 Blanc VF, Hardy JF, Milot J, et al. The oculocardiac reflex: a graphic and statistical analysis in infants and children. Canadian Anaesthetists' Society Journal. 1983; 30(4):360-369.
    100 Schwartz H. Oculocardiac reflex: is prophylaxis necessary? In: Mark LC, Ngai SH (Eds).
    ??Hightlights of Clinical Anesthesiology, New York: Harper and Row . 1971: 111 -114.
    101 Clemente CD. Gray's Anatomy of the Human Body, 30th American edit., Philadelphia: Lea&Febigerl985.
    102 Rouviere H, Delmas A. Anatomie Humaine: Descriptive, Topographique et Fonctionnelle, Tome I, Tete et Cou, lleme edit. Paris: Masson et Cie Editeurs 1974.
    103 Campbell SK, Parker TD, Welker W. Somatotopic organization of the external cuneate nucleus in albino rats. Brain Res. 1974; 77(1): 1-23.
    104 Brown JA, Preul MC, Nimr S. Trigeminocardiac reflexes Can J Anaesth. 1992; 39(3):303-305.
    105 Kumada M, Damapney RAL, Reis DJ. The trigeminal depressor response: a novel vasodepressor response originating from the trigeminal system. Brain Res. 1977; 119(2):305-326.
    106 Brown JA, Preul MC. Trigeminal depressor response during percutaneous microcompression of the trigeminal ganglion for trigeminal neuralgia. Neurosurgery .1988;23 (6): 745-748.
    107 Schaller B, et al. Trigeminocardiac reflex during surgery in the cerebellopontine angle. J Neurosurg. 1999; 90(2): 215-220.
    108 Baxandall ML, Thorn JL. The nasocardiac reflex. Anaesthesia. 1988; 43(6): 480-481.
    109 Prasad KS. Cardiac depression on syringing the ear. A case report. J Laryngol Otol. 1984;98(10): 1013.
    110 Moorthy SS, Krishna G, Elliott CL. Is there an auriculovagal reflex producing cardiac dysrhythmias? Arch Otolaryngol. 1985; 111(9): 631.
    111 Koblank A. Die Nase als Reflexorgan. 1958, Haug. Ulm. Also Fig. 17.
    112 Young AR. Freud's friend fliess. The Journal of Laryngology & Otology. 2002; 116(12):992-995.
    113 Courtiss EH, Gargan TJ, Courtiss GB. Nasal physiology. Ann Plast Surg. 1984;13(3):214-223.
    114 Rock EH. The external ear canal contralateral lower limb reflex: a case report. Ear Nose Throat J. 1992; 71(3): 134-137.
    115 Bradal A. Neurological Anatomy in Relation to Clinical Medicine, 3rd ed., Oxford University Press, New York 1981.
    116 Kerr FW. The divisional organization of afferent fibres of the trigeminal nerve. Brain. 1963;86(12): 721-732.
    117 Kerr FW. The organization of primary afferents in the subnucleus caudalis of the trigeminal: a light and electron microscopic study of degeneration. Brain Res. 1970; 23(2):147-165.
    118 Bossy J. On the presence of a sensory nucleus of the Ⅸ nerve attached to the spinal tract of the Ⅴ nerve. Acta Anat (Basel). 1968; 70(3): 332-340.
    119 Bradal A., Neurological Anatomy in Relation to Clinical Medicine, 3rd ed., Oxford University Press, New York 1981.
    120 张文斌.三叉神经初级传入与孤束核的联系:HRP跨越神经节追踪研究.1990;6(1):97-106.
    121 Dutschmann M, Herbert H. The medical nucleus of the solitary tract mediates the trigeminally evoked pressor response. Neuroreport. 1998; 9(6): 1053-1057.
    122 Ideguchi S, Hotta H, Suzuki, et al. Trigeminally induced cardiovascular reflex responses in spinalized rats. J Auton Nerv Syst. 2000; 79(2-3): 129-135.
    123 Beckstead RM, Norgren R. An autoradiographic examination of the central distribution of the trigeminal, facial, glossopharyngeal, and vagal nerves in the monkey. J Comp Neurol. 1979; 184(3): 455-472.
    124 Contreras RJ, Beckstead RM, Norgren R. The central projections of the trigeminal, facial, glossopharyngeal and vagus nerves: an autoradiographic study in the rat. J Auton Nerv Syst. 1982; 6(3): 303-322.
    125 Takemura M, Sugimoto T, Sakai A. Topographic organization of central terminal region of different sensory branches of the rat mandibular nerve. Exp Neurol. 1987; 96(3): 540-557.
    126 Whitehead MC, Frank ME. Anatomy of the gustatory system in the hamster: central projections of the chorda tympani and the lingual nerve. J Comp Neurol. 1983; 220(4): 378-395.
    127 Nomura S, Yasui Y, Takada M, et al. Trigeminal primary afferent neurons projecting directly to the solitary nucleus in the cat: A transganglionic and retrograde horseradish peroxidase study. Neurosci Lett. 1984; 50(1-3): 257-262.
    128 张文斌,李继硕,李慧民.三叉神经初级传入纤维与孤束核的联系.神经解剖学杂志.1990;6(1):97-106.
    129 张文斌,李继硕,李慧民.三叉神经初级传入成分向孤束核投射的间接途径—HRP跨节和逆行追踪技术的光镜和电镜研究.解剖学报.1992;23(3):253-259.
    130 李振中等.沿迷走神经传入的心脏感觉纤维在豚鼠左心房的分布.解剖学杂志.1998;21(21:102-104.
    131 Massari VJ, Shirahata M, Johnson TA,et al. Substance P immunoreactive nerve terminals in the dorsolateral nucleus of the tractus solitarius: roles in the baroreceptor reflex. Brain Res. 1998; 785(2): 329-340.
    132 Hegarty AA, Felder RB. Antagonism of vasopressin Ⅵ receptors in NTS attenuates baroreflex control of renal nerve activity. Am J Physiol. 1995; 269(3 Pt 2): H 1080-1086.
    133 Deuchars J,Li YW, Kasparov S, et al. Morphological and electrophysiological properties of neurones in the dorsal vagal complex of the rat activated by arterial baroreceptors. J Comp Neurol. 2000; 417(2): 233-249.
    134 Lan CT, Wu WC, Ling EA, et al. Evidence of a direct projection from the cardiovascular-reactive dorsal medulla to the intermediolateral cell column of the spinal cord in cats as revealed by light and electron microscopy. Neuroscience. 1997; 77(2): 521-533.
    135 李玉明,殷树仪.心内神经节的研究进展.解剖学杂志.1998;21(6):564-567.
    136 Penttila J, Vesalainen R, Helminen A, et al. Spontaneous baroreflex sensitivity as a dynamic measure of cardiac anticholinergic drug effect. J Auton Pharmacol. 2001; 21(2):71-78.
    137 Kasparov S, Paton JF. Changes in baroreceptor vagal reflex performance in the developing rat. Pflugers Arch. 1997; 434(4): 438-444.
    138 Toney GM, Mifflin SW. Mediators of contraction-evoked skeletal muscle depressor response in anesthetized rats. J Appl Physiol. 1996; 81(2): 578-585.
    139 Carrow DJ, Aldrete JA, Masden RR, et al. Effects of large doses of intravenous atropine on heart rate and arterial pressure of anesthetized patients. Anesth Analg. 1975; 54(2): 262-266.
    140 Dennison SJ, Merrit VE, Aprison MH, et al. Redefinition of the location of the dorsal(motor) nucleus of the vagus in the rat. Brain Res Bull. 1981; 6(1): 77-81.
    141 Krowicki KZ, Sivarao VD, Abrahams PT, et al. Excitation of dorsal motor vagal neurons evokes non-nicotinic receptor-mediated gastric relaxation. J Auton Nerv Syst. 1999; 77(2-3): 83-89.
    142 Lidums I, Hebbard GS, Holloway RH. Effect of atropine on proximal gastric motor and sensory function in normal subjects. Gut.2000; 47(1): 30-36.
    143 Bruley des Varannes S, Parys V, Ropert A, et al. Erythromycin enhances fasting and postprandial proximal gastric tone in humans. Gastroenterology. 1995; 109(1): 32-39.
    144 Parys V, Bruley des Varannes S, Ropert A, et al. Use of an electronic barostat for measurement of motor response of the proximal stomach to feeding and different nervous stimuli in man. Gastroenterol Clin Biol. 1993; 17(5): 321-328.
    145 Paterson CA, Anvari M, Tougas G, et al. Nitergic and cholinergic Vagal pathway involved in the regulation of canine proximal gastric tone: an in vivo study. Neurogastoenterol Motil.2000; 12(4): 301-306.
    146 Graca JRV, Leal PRL, Gondim FdeAA, et al. Variations in gastric compliance induced by acute blood volume changes in banethetized rats. Braz J Med Biol Res. 2002; 35(3): 405-410.
    147 van Orshoven NP, Oey PL, van Schelven LJ, et al. Effect of gastric distension on cardiovascular parameters: gastrovascular reflex is attenuated in the elderly. J Physiol(Lond). 2004; 555(Pt 2): 573-583.
    148 Graca JR, Leal PR, Gondim FA, et al. A plethysmometric method for gastric compliance studies in anesthetized rats. J Pharmacol Toxicol Methods. 2000; 43(1): 25-30.
    149 王景杰,黄裕新,王健等.c-fos在电针调控大鼠胃运动中的表达及意义.针刺研究.2001;26(4):274-278.
    150 唐家槐,陈玉珍.针刺内关引起幽门运动的观察.中国针灸.1997;16(7):655-656.
    151 池田和久.电针刺激对大鼠胃运动的影响:有关植物神经和外周传入途径的研究.国外医学中医药分册.2001;23(6):355.
    152 森秀太郎.针刺激胃体运动-针作用机序关研究.日针灸治疗会志.1979;27(2):127-131.
    153 森秀太郎等.经穴实验的研究(第2版).日针灸治疗会杂志.1969;18(3):19-21.
    154 Sato A, Schmidt RF. Somatosympathetic reflexes: afferent fibers, central pathways, discharge characteristics. Physiol Rev. 1973(4); 53:916-947.
    155 Xue FW, Ogawa S, Nakamura T, et al. Systemic administration of procaine suppresses the somato-sympathetic reflex discharges in anesthetized cats. J Anesth. 1992; 6(4): 461-466.
    156 Makeham JM, Goodchild AK, Costin NS, et al. Hypercapnia selectively attenuates the somato-sympathetic reflex. Respir Physiol Neurobiol. 2004; 140 (2): 133-143.
    157 Saeki S, Kakishita M, Nakamura T, et al. The effects of intrathecally administered neostigmine on somato-sympathetic reflex potentials. Masui. 2002; 51(12): 1322-1330.
    158 Shimizu J, Ninomiya I, Furukawa K, et al.Augmentation of somato-sympathetic reflex in the ischemic hindlimb of anesthetized rats. J Auton Nerv Syst. 2000; 78 (2-3): 172-176.
    159 Sato A, Schmidt RF. Spinal and supraspinal components of the reflex discharges into lumber and thoracic white rami. J Physiol (Lond). 1971; 212(3): 839-850.
    160 Iriuchijima J, Kumada M. Efferent cardiac vagal discharge of the dog in response to electrical stimulation of sensory nerves. Jpn J Physiol. 1963; 13:599-605.
    161 Kimura A, Sato A, Sato Y, et al. Single electrical shock of a somatic afferent nerve elicits A-and C-reflex discharge in gastric vegal efferent nerves in anesthetized rats. Neurosci Lett. 1996, 210(1): 53-56.
    162 Meng Z, Lu G. Projection linkage from spinal neurons to both lateral cervical nucleus and solitary tract nucleus in the cat. Biol Signals Recept. 2000; 9(1): 38-44.
    163 黄裕新等.胃经穴位电针调节胃运动的神经作用机制.胃肠病学和肝病学杂志.2004;13(4):358-362.
    164 Blanc VF, Hardy J-F, Milot J, et al. The oculocardiac reflex: a graphic and statistical analysis in infants and children. Can Anaesth Soc J. 1983; 30(4): 360-369.
    165 Loewy, A. D. Viruses as transneuronal tracers for defining neural circuits. Neuroscibiobehav Rev. 1998; 22(6): 679-684.
    166 Card JP. Exploring brain circuitry with neurotropic viruses: new horizons in neuroanatomy. Anat Rec. 1998; 253(6): 176-185.
    167 Enquist LW, Cardy JP. Recent advances in the use of neurotropic viruses forcircuit analysis. Neurobiology. 2003; 13(5): 603-606.
    168 杨民,Enguist LW,Card JP,等.用减毒型亲神经性跨神经元传递的假狂犬病毒追踪神经通路.神经解剖学杂志.1996;12(4):317-326.
    169 Card JP. Practical considerations for the use of pseudorabies virus in transneuronal studies of neural circuitry. Neurosci biobehav Rev. 1998; 22(6): 685-694.
    170 Kim ES, Li H, McCulloch PF, et al. Spatial and temporal patterns of transneuronal labeling in CNS neurons after injection of pseudorabies virus into the sciatic nerve of adult rats. Brain Res. 2000; 857(1-2): 41-55.
    171 Card JP, Enquist LW, Moore RY. Neuroinvasiveness of pseudorabies virus injected intracerebrally is dependent on viral concentration and terminal field density. J Comp Neurol. 1999; 407(3): 438-452.
    172 Aston-Jones G, Card JP. Use of pseudorabies virus to delineate multisynaptic circuits in brain: opportunities and limitations. Journal of Neuroscience Methods.2000; 103 (1): 51-61.
    173 Walther D, Takemura M, Uh IG. Fos family number changes in nucleus caudalis after primary efferent stimulation:enhancement of fos B and c-los. Mol Brain Res.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700