Abstract
There is both theoretical and therapeutic interest in establishing whether the signals conveyed by the enkephalins are turned off under the action of a specific peptidase which might, in this case, represent a target for a new class of psychoactive agents. Enkephalinase, a dipeptidyl carboxypeptidase cleaving the Gly3-Phe4 bond of enkephalins1,2 and distinct from angiotensin converting enzyme (ACE)3–6, might be selectively involved in enke-phalinergic transmission. It is a membrane-bound enzyme1,7,8 whose localization in the vicinity of opiate receptors in the central nervous system is suggested by parallel regional1,7,9 and subcellular10 distributions as well as by the effects of lesions9. Such a role is further supported by the ontogenetic development of enkephalinase11,12, its substrate specificity accounting for the increased biological activity of several enkephalin analogues13 and its adaptive increase following chronic treatment with morphine1,14. To investigate the functional role of this enzyme further, we have designed a potent and specific enkephalinase inhibitor. We report here that this compound, thiorphan [(DL-3-mercapto-2-benzylpropanoyl)-glycine; patent no. 8008601] protects the enkephalins from the action of enkephalinase in vitro in nanomolar concentration and in vivo after either intracerebroventricular or systemic administration. In addition, thiorphan itself displays antinociceptive activity which is blocked by naloxone, an antagonist of opiate receptors.
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References
Malfroy, B., Swerts, J. P., Guyon, A., Roques, B. P. & Schwartz, J-C. Nature 276, 523–526 (1978).
Guyon, A. et al. Life Sci. 25, 1605–1612 (1979).
Swerts, J. P., Perdrisot, R., Malfroy, B. & Schwartz, J-C. Eur. J. Pharmac. 53, 209–210 (1979).
Swerts, J. P., Perdrisot, R., Patey, G., De La Baume, S. & Schwartz, J-C. Eur. J. Pharmac. 57, 279–281 (1979).
Sullivan, S., Akil, H., Blacker, D. & Barchas, J. D. in Endogenous and Exogenous Opiate Agonists and Antagonists (ed. Way, E. L.) 357–360 (Pergamon, New York, 1980).
Gorenstein, C. & Snyder, S. H. Life Sci. 25, 2065–2070 (1979).
Sullivan, S., Akil, H. & Barchas, J. D. Commun. Psychopharmac. 2, 525–531 (1979).
Vogel, Z. & Altstein, M. in Endogenous and Exogenous Opiate Agonists and Antagonists (ed. Way, E. L.) 353–356 (Pergamon, New York, 1980).
Malfroy, B., Swerts, J. P., Llorens, C. & Schwartz, J-C. Neurosci. Lett. 11, 329–334 (1979).
De La Baume, S., Patey, G. & Schwartz, J-C. Neuroscience (in the press).
De La Baume, S., Patey, G., Gros, C. & Schwartz, J-C. in Endogenous and Exogenous Opiate Agonists and Antagonists (ed. Way, E. L.) 179–182 (Pergamon, New York, 1980).
Patey, G., De La Baume, S., Gros, C. & Schwartz, J-C. Life Sci. 27, 245–252 (1980).
Fournie-Zaluski, M. C. et al. Biochem. biophys. Res. Commun. 91, 130–135 (1979).
Schwartz, J-C. et al. Adv. Biochem. Psychopharmac. 22, 219–235 (1980).
Quiocho, F. A. & Lipscomb, W. N. Adv. Protein Chem. 15, 1–48 (1971).
Ondetti, M. A., Rubin, B. & Cushman, D. W. Science 196, 441–444 (1977).
Ondetti, M. A. et al. Biochemistry 18, 1427–1430 (1979).
Yang, H. Y. T. & Neff, N. H. J. Neurochem. 19, 2443–2450 (1972).
Erdos, E. G., Johnson, A. R. & Boyden, N. T. Biochem. Pharmac. 27, 843–848 (1978).
Hambrook, J. M., Morgan, B. A., Rance, M. J. & Smith, C. F. Nature 262, 782–783 (1976).
Lane, A. C., Ranee, M. J. & Walter, D. S. Nature 269, 75–76 (1977).
Marks, N., Grynbaum, A. & Neidle, A. Biochem. biophys. Res. Commun. 74, 1552–1559 (1977).
Meek, J. L., Yang, H. Y. T. & Costa, E. Neuropharmacology 16, 151–154 (1977).
Vogel, Z. & Alstein, M. FEBS Lett. 80, 332–336 (1977).
Knight, M. & Klee, W. A. J. biol. Chem. 253, 3843–3847 (1978).
Guyon, A. et al. Biochem. biophys. Res. Commun. 88, 919–926 (1979).
Pert, C. B., Pert, A., Chang, J. K. & Fong, B. T. W. Science 194, 331–332 (1976).
Ben-Bassat, J., Peretz, E. & Sulman, F. G. Archs int. Pharmacodyn. Ther. 122, 434–477 (1959).
Jacob, J., Tremblay, E. C. & Colombel, M. C. Psychopharmacologia 37, 217–223 (1974).
Goldstein, A., Pryor, G. T., Otis, L. S. & Larson, F. Life Sci. 18, 599–604 (1976).
Sewell, R. D. E. & Spencer, P. S. J. Neuropharmacology 15, 683–688 (1976).
Frederickson, R. C. A., Bergers, V. & Edwards, J. D. Science 198, 756–757 (1977).
Woolf, C. J. Brain Res. 190, 578–583 (1980).
Eddy, N. B., May, E. L. & Mosettig, E. J. org. Chem. 17, 321–326 (1952).
Jacob, J. & Blozovski, M. Archs int. Pharmacodyn. Ther. 133, 296–309 (1961).
Stine, S. M., Yang, H. Y. T. & Costa, E. Brain Res. 188, 295–299 (1980).
Llorens, C. et al. Biochem. biophys. Res. Commun. (in the press).
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Roques, B., Fournié-Zaluski, M., Soroca, E. et al. The enkephalinase inhibitor thiorphan shows antinociceptive activity in mice. Nature 288, 286–288 (1980). https://doi.org/10.1038/288286a0
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DOI: https://doi.org/10.1038/288286a0
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