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Bioscience, Biotechnology, and Biochemistry Volume 62, 1998 - Issue 12
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Original Articles

Inhibition by a Capsaicin Antagonist (Capsazepine) of Capsaicin-induced Swimming Capacity Increase in Mice

Kyung-Mi KIMLaboratory of Nutrition Chemistry, Division of Applied Life Sciences, Graduate School of Agriculture, Kyoto University
,
Teruo KAWADALaboratory of Nutrition Chemistry, Division of Applied Life Sciences, Graduate School of Agriculture, Kyoto University
,
Kengo ISHIHARALaboratory of Nutrition Chemistry, Division of Applied Life Sciences, Graduate School of Agriculture, Kyoto University
,
Kazuo INOUELaboratory of Nutrition Chemistry, Division of Applied Life Sciences, Graduate School of Agriculture, Kyoto University
&
Tohru FUSHIKILaboratory of Nutrition Chemistry, Division of Applied Life Sciences, Graduate School of Agriculture, Kyoto University
Pages 2444-2445 | Received 19 Jun 1998, Accepted 12 Aug 1998, Published online: 22 May 2014

  • 1) Kim, K. M., Kawada, T., Ishihara, K., Inoue, K., and Fushiki, T., Increase in swimming endurance capacity of mice by capsaicin-induced adrenal catecholamine secretion. Biosci. Biotech. Biochem., 61, 1718-1723 (1997).
  • 2) Walpole, C. S. J., Bevan, S., Bovermann, G., Boelsterli, J. J., Breckenridge, R., Davies, J. W., Hughes, G. N., James, I., Oberer, L., Winter, J., and Wrigglesworth, R., The discovery of capsazepine, the first competitive antagonist of the sensory neuron excitants capsaicin and resiniferatoxin. J. Med. Chem., 37, 1942-1954, (1994).
  • 3) Anton, A. H. and Sayre, D. F., A study of the factors affecting the aluminum oxide-trihydroxyindole procedure for the analysis of catecholamines. J. Pharmacol. Exptl. Therap., 138, 360-375 (1962).
  • 4) Bevan, S., Hothi, S., Hughes, G., James, I. F., Rang, H. P., Shah, K., Walpole, C. S. J., and Yeats, J. C., Capsazepine: a competitive antagonist of the sensory neurone excitant capsaicin. Br. J. Pharmacol., 107, 544-552 (1992).
  • 5) Vries, D. J. and Blumberg, P. M., Thermoregulatory effects of resiniferatoxin in the mouse. Life Sci., 44, 711-715 (1989).
  • 6) Szallasi, A. and Blumberg, P. M., Resiniferatoxin: a phorbol-related diterpene, acts as an ultrapotent analog capsaicin, the irritant constituent in red pepper. Neurosci., 30, 515-520 (1989).
  • 7) Dray, A., Bettany, J., and Forster, P., Resiniferatoxin: a potent capsaicin-like stimulator of peripheral nociceptors in the neonatal rat tail in vitro. Br. J. Pharmacol., 99, 323-326 (1990).
  • 8) Szallasi, A. and Blumberg, P. M., Resiniferatoxin and its analogue provide novel insights into the pharamacology of the vanilloid (capsaicin) receptor. Life Sci., 47, 1399-1408 (1990).
  • 9) Dickenson, A. H. and Dray, A., Selective antagonism of capsaicin by capsazepine: evidence for a spinal receptor site in capsaicin-induced antinociception. Br. J. Pharmacol., 104, 1045-1049 (1991).
  • 10) Caterina, M. J., Schumacher, M. A., Tominaga, M., Rosen, T. A., Levine, J. D., and Julius, D., The capsaicin receptor: a heat-activated ion channel in the pain pathway. Nature, 389, 816-824 (1997).
  • 11) Clapham, D. E., Some like it hot: spicing ion channels. Nature, 389, 783-784 (1997).

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