Abstract
Exposure to stress has been associated with alterations in both immune function and tumor development in man and laboratory animals. In the present study, we investigated the effect of a particular type of inescapable footshock stress, known to cause an opioid mediated form of analgesia, on survival time of female Fischer 344 rats injected with a mammary ascites tumor. Rats subjected to inescapable footshock manifested an enhanced tumor growth indicated by a decreased survival time and decreased percent survival. This tumor enhancing effect of stress was prevented by the opiate antagonist, naltrexone, suggesting a role for endogenous opioid peptides in this process. In the absence of stress, naltrexone did not affect tumor growth. © 1983.
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Lewis, J. W., Shavit, Y., Terman, G. W., Nelson, L. R., Gale, R. P., & Liebeskind, J. C. (1983). Apparent involvement of opioid peptides in stress-induced enhancement of tumor growth. Peptides, 4(5), 635–638. https://doi.org/10.1016/0196-9781(83)90010-4
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