Abstract
After years of extensive usage, morphine is still regarded as the most powerful pharmacological tool for control of pain. Despite this long record of success in the clinics, it is clear that morphine is not an analgesic, in that pain is not obliterated at systemic dosages that leave respiration intact in man (Javert and Hardy, 1951). Clinical patients report that pain can be elicited in the presence of morphine. Also, the effects of morphine on psychophysical ratings of phasically elicited pain are subtle in comparison with subjective estimates of clinical effectiveness (Beecher, 1957). This disparity of clinical and experimental findings has led to a number of hypotheses concerning the primary actions of morphine: (a) Morphine has been claimed to be an anxiolytic, and its action has been likened to the effects of frontal lobotomy, which is said to attenuate the emotional reactions to pain without disturbing the primary sensations of pain (Freeman and Watts, 1948).
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© 1984 The Wenner-Gren Center
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Vierck, C.J., Cooper, B.Y., Cohen, R.H., Yeomans, D.C., Franzén, O. (1984). Effects of Systemic Morphine on Monkeys and Man: Generalized Suppression of Behavior and Preferential Inhibition of Pain Elicited by Unmyelinated Nociceptors. In: von Euler, C., Franzén, O., Lindblom, U., Ottoson, D. (eds) Somatosensory Mechanisms. Wenner-Gren Center International Symposium Series. Palgrave Macmillan, London. https://doi.org/10.1007/978-1-349-07292-7_22
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DOI: https://doi.org/10.1007/978-1-349-07292-7_22
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