用户名: 密码: 验证码:
Application of quinidine on rat sciatic nerve decreases the amplitude and increases the latency of evoked responses
详细信息    查看全文
  • 作者:Kuang-I Cheng (1) (2) (3)
    I-Ling Lin (4)
    Lin-Li Chang (5)
    I-Ming Jou (6)
    Chung-Sheng Lai (7)
    Jhi-Joung Wang (8)
    Hung-Chen Wang (1) (9)
    Aij-Lie Kwan (10) (11)
  • 关键词:Quinidine ; Sciatic nerve ; Somato ; sensory evoked potential ; Compound muscle action potentials
  • 刊名:Journal of Anesthesia
  • 出版年:2014
  • 出版时间:August 2014
  • 年:2014
  • 卷:28
  • 期:4
  • 页码:559-568
  • 全文大小:3,451 KB
  • 参考文献:1. Pugsley MK, Walker MJ, Saint DA. Block of NA+ and K+ currents in rat ventricular myocytes by quinacainol and quinidine. Clin Exp Pharmacol Physiol. 2005;32(1-):60-. CrossRef
    2. Singh BN, Vaughan Williams EM. The effect of amiodarone, a new anti-anginal drug, on cardiac muscle. Br J Pharmacol. 1970;39(4):657-7.
    3. Deffois A, Fage D, Carter C. Inhibition of synaptosomal veratridine-induced sodium influx by antidepressants and neuroleptics used in chronic pain. Neurosci Lett. 1996;220(2):117-0. CrossRef
    4. Fozzard HA, Lee PJ, Lipkind GM. Mechanism of local anesthetic drug action on voltage-gated sodium channels. Curr Pharm Des. 2005;11(21):2671-6. CrossRef
    5. Ragsdale DSMJ, Scheuer T, Catterall WA. Common molecular determinants of local anesthetic, antiarrhythmic, and anticonvulsant block of voltage-gated Na+ channels. Proc Natl Acad Sci USA. 1996;93:9270-. CrossRef
    6. Packer DL, Grant AO, Strauss HC, Starmer CF. Characterization of concentration- and use-dependent effects of quinidine from conduction delay and declining conduction velocity in canine Purkinje fibers. J Clin Invest. 1989;83(6):2109-9. CrossRef
    7. Nattel S. Relationship between use-dependent effects of antiarrhythmic drugs on conduction and / Vmax in canine cardiac Purkinje fibers. J Pharmacol Exp Ther. 1987;241(1):282-.
    8. Varro AEV, Surawicz B. Frequency-dependent effects of several class I antiarrhythmic drugs on / Vmax of action potential upstroke in canine cardiac Purkinje fibers. J Cardiovasc Pharmacol. 1985;7:482-2. CrossRef
    9. Pallandi RT, Campbell TJ. Selective depression of conduction of premature action potentials in canine Purkinje fibres by class Ib antiarrhythmic drugs: comparison with Ia and Ic drugs. Cardiovasc Res. 1988;22(3):171-. CrossRef
    10. Hara Y, Tamagawa M, Nakaya H. The effects of ketamine on conduction velocity and maximum rate of rise of action potential upstroke in guinea pig papillary muscles: comparison with quinidine. Anesth Analg. 1994;79(4):687-3. CrossRef
    11. Costard-Jaeckle A, Liem LB, Franz MR. Frequency-dependent effect of quinidine, mexiletine, and their combination on postrepolarization refractoriness in vivo. J Cardiovasc Pharmacol. 1989;14(6):810-. CrossRef
    12. Tzeng JI, Cheng KI, Huang KL, Chen YW, Chu KS, Chu CC, Wang JJ. The cutaneous analgesic effect of class I antiarrhythmic drugs. Anesth Analg. 2007;104(4):955-. CrossRef
    13. Jou IM, Chu KS, Chen HH, Chang PJ, Tsai YC. The effects of intrathecal tramadol on spinal somatosensory-evoked potentials and motor-evoked responses in rats. Anesth Analg. 2003;96(3):783-. CrossRef
    14. Jou IM, Lai KA, Shen CL, Yamano Y. Changes in conduction, blood flow, histology, and neurological status following acute nerve-stretch injury induced by femoral lengthening. J Orthop Res. 2000;18(1):149-5. CrossRef
    15. Geuna S, Tos P, Battiston B, Guglielmone R. Verification of the two-dimensional disector, a method for the unbiased estimation of density and number of myelinated nerve fibers in peripheral nerves. Ann Anat. 2000;182(1):23-4. CrossRef
    16. Nuwer M. Monitoring spinal cord surgery with cortical somatosensory evoked potentials. In: Desmedt J, editor. Neuromonitoring in surgery. Amsterdam: Elsevier; 1989. p. 151-4.
    17. Ogata NOY. Molecular diversity of structure and function of the voltage-gated Na+ channels. Jpn J Pharmacol. 2002;88:365-7. CrossRef
    18. Fukuoka TKK, Yamanaka H, Obata K, Dai Y, Noguchi K. Comparative study of the distribution of the alpha-subunits of voltage-gated sodium channels in normal and axotomized rat dorsal root ganglion neurons. J Comp Neurol. 2008;510(2):188-06. CrossRef
    19. Fukuoka TKK, Noguchi K. Laminae-specific distribution of alpha-subunits of voltage-gated sodium channels in the adult rat spinal cord. Neuroscience. 2010;169(3):994-006. CrossRef
    20. Leszczynska KKS. A sciatic nerve blockade method to differentiate drug-induced local anesthesia from neuromuscular blockade in mice. J Pharmacol Toxicol Methods. 1992;27:85-3. CrossRef
    21. Revenko SV, Khodorov BI, Shapovalova LM. Blockade of the sodium and potassium channels of a myelinated nerve fiber by quinidine. Neirofiziologiia. 1982;14(3):324-0.
    22. Tsai YC, Chang PJ, Jou IM. Direct tramadol application on sciatic nerve inhibits spinal somatosensory evoked potentials in rats. Anesth Analg. 2001;92(6):1547-1. CrossRef
    23. Yeola SW, Rich TC, Uebele VN, Tamkun MM, Snyders DJ. Molecular analysis of a binding site for quinidine in a human cardiac delayed rectifier K+ channel. Role of S6 in antiarrhythmic drug binding. Circ Res. 1996;78(6):1105-4. CrossRef
    24. Appel SB, Liu Z, McElvain MA, Brodie MS. Ethanol excitation of dopaminergic ventral tegmental area neurons is blocked by quinidine. J Pharmacol Exp Ther. 2003;306(2):437-6. CrossRef
    25. Smith FL, Lindsay RJ. Enhancement of bupivacaine local anesthesia with the potassium channel blocker ibutilide. Eur J Pain. 2007;11(5):551-. CrossRef
  • 作者单位:Kuang-I Cheng (1) (2) (3)
    I-Ling Lin (4)
    Lin-Li Chang (5)
    I-Ming Jou (6)
    Chung-Sheng Lai (7)
    Jhi-Joung Wang (8)
    Hung-Chen Wang (1) (9)
    Aij-Lie Kwan (10) (11)

    1. Graduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan
    2. Department of Anesthesiology, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan
    3. Department of Anesthesiology, Faculty of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan
    4. Department of Medical Laboratory Science and Biotechnology, College of Health Sciences, Kaohsiung Medical University, Kaohsiung, Taiwan
    5. Department of Microbiology, Graduate Institute of Medicine, Faculty of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan
    6. Departments of Orthopedics, College of Medicine, National Cheng Kung University, Tainan, Taiwan
    7. Division of Plastic and Reconstructive Surgery, Department of Surgery, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan
    8. Department of Medical Research, Chi-Mei Medical Center, Tainan, Taiwan
    9. Department of Neurosurgery, Chang Gung Memorial Hospital-Kaohsiung Medical Center, Chang Gung University College of Medicine, Kaohsiung, Taiwan
    10. Department of Surgery, Faculty of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan
    11. Department of Neurosurgery, Kaohsiung Medical University, 100 Shih-Chuan 1st Road, Kaohsiung, 807, Taiwan
  • ISSN:1438-8359
文摘
Purpose Multi-modality electrophysiological techniques were performed to assess the effects of quinidine on peripheral nerve conduction. Methods Twenty-seven rats were treated with 1, 3, and 5?μmol quinidine in 0.1?ml 5?% glucose. The mixed-nerve somato-sensory evoked potential (M-SSEP), dermatomal-SSEP (D-SSEP), and compound muscle action potentials (CMAP) were evoked and recorded. After positioning Gelfoam strips saturated with quinidine and 5?% glucose around the left and right sciatic nerves, potentials were measured at baseline, immediately after treatment, every 15?min for the 1st hour, and every 30?min for the next 3?h. After 2 weeks, the walking behaviors and potentials were again analyzed and myelinated fibers in the sciatic nerve were counted. Results Quinidine applied directly to sciatic nerves reduced the amplitude and prolonged the latency in SSEPs and CMAP, compared to baseline and the contralateral right limbs (controls). This persisted for at least 4?h. After 2 weeks, electrophysiological tests and walking behavior showed no significant difference between the controls and experimental limbs. There was also no difference in the number of myelinated fibers in the sciatic nerves. Conclusions Quinidine decreases amplitude and prolongs latency in the sciatic nerve in a dose-related manner without local neural toxicity.

© 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