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Journal articles on the topic 'Superior Cervical Ganglion'

Author: Grafiati

Published: 4 June 2021

Last updated: 4 March 2023

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1

Nastenko, A. O., H. E. Purnyn, and N. S. Veselovsky. "PHYSIOLOGICAL FUNCTIONS DISORDERS OF THE SUPERIOR CERVICAL GANGLION NEURONS IN DIABETES MELLITUS." Fiziolohichnyĭ zhurnal 68, no. 1 (2022): 74–86. http://dx.doi.org/10.15407/fz68.01.074.

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A large number of extra- and intramural ganglia in humans and animals exist. All pathways of central regulation of vegetative functions and peripheral reflex pathways pass through them, providing coordinated automatic activity of many organs and tissues. It is well known that sympathetic and sensory neurons are affected in the early stages of diabetes. Patients with diabetes often have autonomic neuropathies. They suffer from disorders of the cardiovascular system and vessels functions, from disorders of the thermoregulatory and pupilomotor functions. These disorders may be the result of the s

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2

Jobling, Phillip, and Ian L. Gibbins. "Electrophysiological and Morphological Diversity of Mouse Sympathetic Neurons." Journal of Neurophysiology 82, no. 5 (1999): 2747–64. http://dx.doi.org/10.1152/jn.1999.82.5.2747.

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We have used multiple-labeling immunohistochemistry, intracellular dye-filling, and intracellular microelectrode recordings to characterize the morphological and electrical properties of sympathetic neurons in the superior cervical, thoracic, and celiac ganglia of mice. Neurochemical and morphological characteristics of neurons varied between ganglia. Thoracic sympathetic ganglia contained three main populations of neurons based on differential patterns of expression of immunoreactivity to tyrosine hydroxylase, neuropeptide Y (NPY) and vasoactive intestinal peptide (VIP). In the celiac ganglio

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3

Edvinsson, L., H. Hara, and R. Uddman. "Retrograde Tracing of Nerve Fibers to the Rat Middle Cerebral Artery with True Blue: Colocalization with Different Peptides." Journal of Cerebral Blood Flow & Metabolism 9, no. 2 (1989): 212–18. http://dx.doi.org/10.1038/jcbfm.1989.31.

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The origin of nerve fibers to the rat middle cerebral artery was studied by retrograde tracing with the fluorescent tracer True Blue (TB) in combination with immunocytochemistry to known perivascular peptides. Application of TB to the middle cerebral artery labeled nerve cell bodies in the ipsilateral superior cervical ganglion, the otic ganglion, the sphenopalatine ganglion, the trigeminal ganglion, and the cervical dorsal root ganglion at level C2. A few labeled nerve cell bodies were seen in contralateral ganglia. Judging from the number and intensity of the labeling, the superior cervical

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4

Liutkienė, Gineta, Rimvydas Stropus, Anita Dabužinskienė, and Mara Pilmane. "Structural changes of the human superior cervical ganglion following ischemic stroke." Medicina 43, no. 5 (2007): 390. http://dx.doi.org/10.3390/medicina43050048.

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Objective. The sympathetic nervous system participates in the modulation of cerebrovascular autoregulation. The most important source of sympathetic innervation of the cerebral arteries is the superior cervical ganglion. The aim of this study was to investigate signs of the neurodegenerative alteration in the sympathetic ganglia including the evaluation of apoptosis of neuronal and satellite cells in the human superior cervical ganglion after ischemic stroke, because so far alterations in human sympathetic ganglia related to the injury to peripheral tissue have not been enough analyzed. Materi

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5

Rubin, E. "Development of the rat superior cervical ganglion: ganglion cell maturation." Journal of Neuroscience 5, no. 3 (1985): 673–84. http://dx.doi.org/10.1523/jneurosci.05-03-00673.1985.

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6

Wang, Feng-Bin. "Superior Cervical Ganglion: Axonal Passage and Inputs." Adaptive Medicine 11, no. 1 (2019): 12–17. http://dx.doi.org/10.4247/am.2019.abj226.

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7

Chunhabundit, P., S. Thongpila, and R. Somana. "Microvascularization of the Rat Superior Cervical Ganglion." Cells Tissues Organs 143, no. 1 (1992): 54–58. http://dx.doi.org/10.1159/000147228.

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8

Ariano, Marjorie A., and Sharon L. Kenny. "Peptide coincidence in rat superior cervical ganglion." Brain Research 340, no. 1 (1985): 181–85. http://dx.doi.org/10.1016/0006-8993(85)90791-7.

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9

Baffi, Judit, T. Go¨rcs, Felicia Slowik, et al. "Neuropeptides in the human superior cervical ganglion." Brain Research 570, no. 1-2 (1992): 272–78. http://dx.doi.org/10.1016/0006-8993(92)90591-v.

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10

Jeon, Seayuong, Jinpyeong Kim, and Euigee Hwang. "Origin and Distribution of NADPH Diaphorase-Positive Nerves in Rat Nasal Mucosa." Annals of Otology, Rhinology & Laryngology 106, no. 8 (1997): 688–92. http://dx.doi.org/10.1177/000348949710600814.

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The aim of this study was to localize the distribution of (reduced) nicotinamide-adenine dinucleotide phosphate (NADPH) diaphorase-positive nerves in the rat nasal mucosa by NADPH diaphorase histochemistry, and to determine its origin by utilizing retrograde tracing with Fluoro-Gold (FG). Fine varicosities of NADPH diaphorase-positive nerve fibers were distributed around blood vessels (arterioles in particular), submucosal glands, and the subepithelial layer of the nasal mucosa. Most of the ganglion cells and nerve fibers in the sphenopalatine ganglion, and a few ganglion cells in the trigemin

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11

Kobayashi, Haruo, Sumiko Mochida, and Susumu Y. Takahashi. "Intracellular transduction mechanisms for the slow synaptic events." Canadian Journal of Physiology and Pharmacology 70, S1 (1992): S44—S50. http://dx.doi.org/10.1139/y92-242.

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Electrical activities of the postganglionic neurons in the superior cervical ganglia of rabbits are modulated in various ways following activation of the subtypes of muscarinic acetylcholine receptors, (i) M1 receptors mediate a slow depolarization consisting of at least three types of ionic conductance changes, and one of these is possibly mediated by cyclic GMP. (ii) M2 receptors mediate a slow hyperpolarization that seems to be generated by inositol triphosphate derived from phosphatidylinositol breakdown. (iii) M2 receptors also cause, through an activation of C kinase, a suppression of Ca

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12

Manuel, Nimmy, Lekha K. S., Lola Das, and Seena N. "Surgical anatomy of cervical sympathetic trunk: a cadaveric study." International Journal of Research in Medical Sciences 10, no. 2 (2022): 400. http://dx.doi.org/10.18203/2320-6012.ijrms20220282.

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Background: Cervical sympathetic trunk (CST) is at risk of injury during surgical procedures of cervical spine and may result in Horner’s syndrome. The purpose of present study was to clearly describe the surgical anatomy of CST with respect to the surrounding structures and to analyse the anatomical variations.Methods: In this cross-sectional study, 50 cervical sympathetic chains were studied by bilateral neck dissections of 25 formalin fixed human cadavers from the Department of Anatomy, Government medical college Thrissur.Results: Cervical sympathetic chain was found inside the carotid shea

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13

Durbec, P. L., L. B. Larsson-Blomberg, A. Schuchardt, F. Costantini, and V. Pachnis. "Common origin and developmental dependence on c-ret of subsets of enteric and sympathetic neuroblasts." Development 122, no. 1 (1996): 349–58. http://dx.doi.org/10.1242/dev.122.1.349.

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c-ret encodes a tyrosine kinase receptor that is necessary for normal development of the mammalian enteric nervous system. Germline mutations in c-ret lead to congenital megacolon in humans, while a loss-of-function allele (ret.k-) causes intestinal aganglionosis in mice. Here we examine in detail the function of c-ret during neurogenesis, as well as the lineage relationships among cell populations in the enteric nervous system and the sympathetic nervous system that are dependent on c-ret function. We report that, while the intestine of newborn ret.k- mice is devoid of enteric ganglia, the es

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14

Sheng, Hong, Gerard D. Gagne, Takahiro Matsumoto, Mahlon F. Miller, Ulrich Förstermann, and Ferid Murad. "Nitric Oxide Synthase in Bovine Superior Cervical Ganglion." Journal of Neurochemistry 61, no. 3 (1993): 1120–26. http://dx.doi.org/10.1111/j.1471-4159.1993.tb03628.x.

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15

Smolen, Arnold J., and Patricia Beaston-Wimmer. "Dendritic development in the rat superior cervical ganglion." Developmental Brain Research 29, no. 2 (1986): 245–52. http://dx.doi.org/10.1016/0165-3806(86)90100-8.

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16

Ichikawa, H., R. Terayama, T. Yamaai, and T. Sugimoto. "Peptide 19 in the rat superior cervical ganglion." Neuroscience 161, no. 1 (2009): 86–94. http://dx.doi.org/10.1016/j.neuroscience.2009.03.018.

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17

Watterson, J. G., R. Good, E. Moses, M. T. W. Hearn, and L. Austin. "Phosphorylation of Superior Cervical Ganglion Proteins During Regeneration." Journal of Neurochemistry 52, no. 6 (1989): 1700–1707. http://dx.doi.org/10.1111/j.1471-4159.1989.tb07247.x.

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18

Purnyn, H., O. Rikhalsky, S. Fedulova, and N. Veselovsky. "Transmission pathways in the rat superior cervical ganglion." Neurophysiology 39, no. 4-5 (2007): 347–49. http://dx.doi.org/10.1007/s11062-007-0053-2.

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19

Narouze, Samer. "Ultrasound-guided Stellate Ganglion Block Successfully Prevented Esophageal Puncture." November 2007 6;10, no. 6;11 (2007): 747–52. http://dx.doi.org/10.36076/ppj.2007/10/747.

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Stellate ganglion block is utilized in the diagnosis and management of various vascular disorders and sympathetically mediated pain in the upper extremity, head and neck. The cervical sympathetic chain is composed of superior, middle, intermediate, and inferior cervical ganglia. However, in approximately 80% of the population, the inferior cervical ganglion is fused with the first thoracic ganglion, forming the stellate ganglion also known as cervicothoracic ganglion. The stellate ganglion lies medial to the scalene muscles, lateral to the longus coli muscle, esophagus and trachea along with t

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20

Itakura, Toru, Ichiro Kamei, Kunio Nakai, et al. "Autotransplantation of the superior cervical ganglion into the brain." Journal of Neurosurgery 68, no. 6 (1988): 955–59. http://dx.doi.org/10.3171/jns.1988.68.6.0955.

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✓ The superior cervical ganglion (SCG) of rats was transplanted into their own parietal cortex. Four weeks after implantation, catecholamine histofluorescence revealed many transplanted catecholamine cells in the cortex. However, no fibers extended from the transplanted tissue to the cerebral cortex. In a second group of rats which had been pretreated with 6-hydroxydopamine (a specific neurotoxin to the catecholamine neuron), some showed extension of catecholamine fibers to the cerebral cortex. To simulate an animal model of Parkinson's disease, MPTP (1-methyl-4-phenyl-1,2,5,6-tetrahydropyridi

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21

TOMINAGA, TAKESHI, HIDEICHI SHINKAWA, and JIRO HOZAWA. "Influence of Superior Cervical Ganglion Stimulation on Vestibular Function." Nippon Jibiinkoka Gakkai Kaiho 97, no. 5 (1994): 905–11. http://dx.doi.org/10.3950/jibiinkoka.97.905.

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22

Kawai, Tomoyuki, and Minoru Watanabe. "Spike-afterhyperpolarizing current (IAHP) in rat superior cervical ganglion." Japanese Journal of Pharmacology 52 (1990): 328. http://dx.doi.org/10.1016/s0021-5198(19)55808-5.

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23

Tajti, Janos, Sebastian Möller, Rolf Uddman, Istvan Bodi, and Lars Edvinsson. "The human superior cervical ganglion: neuropeptides and peptide receptors." Neuroscience Letters 263, no. 2-3 (1999): 121–24. http://dx.doi.org/10.1016/s0304-3940(99)00115-9.

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24

Wright, L. L., J. I. Luebke, and A. E. Elshaar. "Target-specific subpopulations of rat superior cervical ganglion neurones." Journal of the Autonomic Nervous System 33, no. 2 (1991): 105–6. http://dx.doi.org/10.1016/0165-1838(91)90143-q.

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25

Capuzzo, A., P. G. Borasio, and E. Fabbri. "Presynaptic muscarinic receptors in guinea pig superior cervical ganglion." Neuroscience Letters 104, no. 1-2 (1989): 88–92. http://dx.doi.org/10.1016/0304-3940(89)90334-0.

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26

Bucci, Giovanna, Christian Vogl, Cesare Usai, Sumiko Mochida, and Gary J. Stephens. "Inhibitory Cav2.2 Peptides Effects in Superior Cervical Ganglion Neurones." Biophysical Journal 102, no. 3 (2012): 432a—433a. http://dx.doi.org/10.1016/j.bpj.2011.11.2369.

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27

Watterson, J. G., R. Good, M. T. W. Hearn, and L. Austin. "Protein Phosphorylation in Intact Superior Cervical Ganglion During Regeneration." Journal of Neurochemistry 55, no. 2 (1990): 588–93. http://dx.doi.org/10.1111/j.1471-4159.1990.tb04174.x.

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28

Newberry, N. R., and K. E. Roberts. "Muscarinic pharmacology of the guinea-pig superior cervical ganglion." European Journal of Pharmacology 183, no. 5 (1990): 2043–44. http://dx.doi.org/10.1016/0014-2999(90)92406-9.

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29

Terayama, Yukitsugu, Tomohiro Matsuyama, Masayasu Matsumoto, Takenobu Kamada, Akio Wanaka, and Masaya Tohyama. "Enkephalinergic system in rat superior cervical ganglion: Immunohistochemical study." Neuroscience Research Supplements 9 (January 1989): 131. http://dx.doi.org/10.1016/0921-8696(89)90827-x.

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30

Bachoo, M., and C. Polosa. "An AF-DX 116 sensitive inhibitory mechanism modulates nicotinic and muscarinic transmission in cat superior cervical ganglion in the presence of anticholinesterase." Canadian Journal of Physiology and Pharmacology 70, no. 12 (1992): 1535–41. http://dx.doi.org/10.1139/y92-220.

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The effect of the muscarinic receptor antagonist AF-DX 116 on the inhibitory action of muscarinic agonists and on responses mediated by nicotinic or muscarinic ganglionic transmission was studied in the superior cervical ganglion of the anesthetized cat. The postganglionic compound action potential evoked by cervical sympathetic trunk stimulation was depressed by methacholine or acetylcholine (ACh) injected into the ganglionic arterial supply. The depression was blocked by AF-DX 116. The compound action potentials evoked by preganglionic stimulus trains were also depressed when the intratrain

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31

Getsy, Paulina M., Gregory A. Coffee, Yee-Hsee Hsieh, and Stephen J. Lewis. "The superior cervical ganglia modulate ventilatory responses to hypoxia independently of preganglionic drive from the cervical sympathetic chain." Journal of Applied Physiology 131, no. 2 (2021): 836–57. http://dx.doi.org/10.1152/japplphysiol.00216.2021.

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We present data showing that the ventilatory responses elicited by a hypoxic gas challenge in male C57BL6 mice with bilateral superior cervical ganglionectomy are not equivalent to those reported for mice with bilateral transection of the cervical sympathetic chain. These data suggest that hypoxic gas challenge may directly activate subpopulations of superior cervical ganglion (SCG) cells, including small intensely fluorescent cells and/or principal SCG neurons, independently of preganglionic cervical sympathetic chain drive.

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32

Hanani, Menachem, Anna Caspi, and Vitali Belzer. "Peripheral inflammation augments gap junction-mediated coupling among satellite glial cells in mouse sympathetic ganglia." Neuron Glia Biology 6, no. 1 (2010): 85–89. http://dx.doi.org/10.1017/s1740925x10000025.

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Intercellular coupling by gap junctions is one of the main features of glial cells, but very little is known about this aspect of satellite glial cells (SGCs) in sympathetic ganglia. We used the dye coupling method to address this question in both a prevertebral ganglion (superior mesenteric) and a paravertebral ganglion (superior cervical) of mice. We found that in control ganglia, the incidence of dye coupling among SGCs that form the envelope around a given neuron was 10–20%, and coupling between SGCs around different envelopes was rare (1.5–3%). The dye injections also provided novel infor

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33

Zivkovic, Vladimir, Natalija Stefanovic, Tatjana Djurovic-Filipovic, et al. "Patterns of lipofuscin accumulation in ganglionic nerve cells of superior cervical ganglion in humans." Vojnosanitetski pregled 65, no. 10 (2008): 738–42. http://dx.doi.org/10.2298/vsp0810738z.

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Background/Aim. Considering available literature lipofuscin is a classical age pigment of postmitotic cells, and a consistently recognized phenomenon in humans and animals. Lipofuscin accumulation is characteristic for nerve cells that are postmitotic. This research was focused on lipofuscin accumulation in ganglionic cells (GC) (postganglionic sympathetic cell bodies) of superior cervical ganglion in humans during ageing. Methods. We analysed 30 ganglions from cadavers ranging from 20 to over 80 years of age. As material the tissue samples were used from the middle portion of the ganglion, wh

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34

Lee, Joo Yeon, Jeong Hyun Lee, Joon Seon Song, et al. "Superior Cervical Sympathetic Ganglion: Normal Imaging Appearance on 3T-MRI." Korean Journal of Radiology 17, no. 5 (2016): 657. http://dx.doi.org/10.3348/kjr.2016.17.5.657.

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35

KONDO, Mari. "Studies on the nerve cells of the superior cervical ganglion." Japanese Heart Journal 27, no. 4 (1986): 580. http://dx.doi.org/10.1536/ihj.27.580.

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36

YAO, Li-jun, Gang WANG, Kun-fu OU-YANG, et al. "Ca2+ sparks and Ca2+ glows in superior cervical ganglion neurons1." Acta Pharmacologica Sinica 27, no. 7 (2006): 848–52. http://dx.doi.org/10.1111/j.1745-7254.2006.00402.x.

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37

Derkach, V. A., R. A. North, A. A. Selyanko, and V. I. Skok. "Single channels activated by acetylcholine in rat superior cervical ganglion." Journal of Physiology 388, no. 1 (1987): 141–51. http://dx.doi.org/10.1113/jphysiol.1987.sp016606.

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38

Newberry Clare J. Watkins, Nigel R., Andreja Volenec, and Thomas P. Flanigan. "5-HT2B receptor mRNA in guinea pig superior cervical ganglion." NeuroReport 7, no. 18 (1996): 2909–12. http://dx.doi.org/10.1097/00001756-199611250-00020.

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39

Kammermeier, Paul J., and Stephen R. Ikeda. "Metabotropic glutamate receptor expression in the rat superior cervical ganglion." Neuroscience Letters 330, no. 3 (2002): 260–64. http://dx.doi.org/10.1016/s0304-3940(02)00822-4.

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40

Gao, Hui-Ling, He Xu, Xin Wang, Annica Dahlstrom, Liping Huang, and Zhan-You Wang. "Expression of zinc transporter ZnT7 in mouse superior cervical ganglion." Autonomic Neuroscience 140, no. 1-2 (2008): 59–65. http://dx.doi.org/10.1016/j.autneu.2008.04.002.

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41

Fueri, C., M. Faudon, M. C. Barrit, and F. Hery. "Serotonin release from the superior cervical ganglion of the cat." Neurochemistry International 7, no. 5 (1985): 843–52. http://dx.doi.org/10.1016/0197-0186(85)90040-3.

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42

Hawcock, A. B., F. H. Marshall, I. J. M. Beresford, and R. M. Hagan. "Two NK1 agonist responses in the rat superior cervical ganglion." Neuropeptides 24, no. 4 (1993): 234. http://dx.doi.org/10.1016/0143-4179(93)90247-8.

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43

Henley, Rachel, Vidya Chandrasekaran, and Cecilia Giulivi. "Computing neurite outgrowth and arborization in superior cervical ganglion neurons." Brain Research Bulletin 144 (January 2019): 194–99. http://dx.doi.org/10.1016/j.brainresbull.2018.12.001.

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44

Reuss, Stefan, and Robert Y. Moore. "Neuropeptide Y-Containing Neurons in the Rat Superior Cervical Ganglion." Journal of Pineal Research 6, no. 4 (1989): 307–16. http://dx.doi.org/10.1111/j.1600-079x.1989.tb00426.x.

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45

Vivas, Oscar, Martin Kruse, and Bertil Hille. "Nerve Growth Factor Sensitizes Superior Cervical Ganglion Neurons to Bradykinin." Biophysical Journal 106, no. 2 (2014): 541a. http://dx.doi.org/10.1016/j.bpj.2013.11.3014.

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46

Melo, Samanta Rios, Jens Randel Nyengaard, Felipe da Roza Oliveira, et al. "The Developing Left Superior Cervical Ganglion of Pacas(Agouti paca)." Anatomical Record: Advances in Integrative Anatomy and Evolutionary Biology 292, no. 7 (2009): 966–75. http://dx.doi.org/10.1002/ar.20918.

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47

Chen, Chu, and Geoffrey G. Schofield. "Ca2+ currents of fast blue-labeled superior cervical ganglion neurons." Journal of Neuroscience Methods 45, no. 1-2 (1992): 63–69. http://dx.doi.org/10.1016/0165-0270(92)90044-e.

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48

Alain, VERNA. "DISTRIBUTION OF NADPH-DIAPHORASE IN THE RABBIT SUPERIOR CERVICAL GANGLION." Biology of the Cell 79, no. 1 (1993): 91. http://dx.doi.org/10.1016/0248-4900(93)90304-w.

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49

Tredici, G., G. Cavaletti, M. G. Petruccioli, D. Fabbrica, and G. Pizzini. "Degenerative processes in ganglionic neurons of the superior cervical ganglion in cisplatin-treated rats." Journal of the Autonomic Nervous System 43 (April 1993): 111. http://dx.doi.org/10.1016/0165-1838(93)90300-j.

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50

H�pp�l�, O., S. Soinila, H. P�iv�rinta, P. Panula, and O. Er�nk�. "Histamine-immunoreactive cells in the superior cervical ganglion and in the coeliac-superior mesenteric ganglion complex of the rat." Histochemistry 82, no. 1 (1985): 1–3. http://dx.doi.org/10.1007/bf00502083.

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