1993
DOI: 10.1007/978-3-642-77540-6_12
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Opioid Systems and Stress

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Cited by 14 publications
(6 citation statements)
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“…Endogenous opioid peptides may integrate these responses to stress (Boissy, 1995). Opioids are involved in many responses to stress (Przewlocki, 1993), regulate various endocrine systems, including the hypothalamic-pituitary-adrenocortical (HPA) axis, and underlie the phenomenon of stress-induced analgesia. Rushen and Ladewig (1991) detected an opioid-based stressinduced analgesia in restrained pigs and found that naloxone (a generalized opioid antagonist with a strong affinity for µ-opioid receptors) increased HPA responses and vocalization in response to restraint.…”
Section: Introductionmentioning
confidence: 99%
“…Endogenous opioid peptides may integrate these responses to stress (Boissy, 1995). Opioids are involved in many responses to stress (Przewlocki, 1993), regulate various endocrine systems, including the hypothalamic-pituitary-adrenocortical (HPA) axis, and underlie the phenomenon of stress-induced analgesia. Rushen and Ladewig (1991) detected an opioid-based stressinduced analgesia in restrained pigs and found that naloxone (a generalized opioid antagonist with a strong affinity for µ-opioid receptors) increased HPA responses and vocalization in response to restraint.…”
Section: Introductionmentioning
confidence: 99%
“…Furthermore, a number of experiments have demonstrated that stress can modify passive and active avoidance response behaviors (2 -6). In this regard, it is well understood that opioid peptides are closely involved in stress circuits, being released under stressful conditions (7). Endogenous opioids have also been implicated as mediators of stress-induced analgesia (SIA) (8)(9)(10).…”
mentioning
confidence: 99%
“…The general stimulatory role that opiods have on Prl release is believed to be mediated by the hypothalamic-dopaminergic tuberoinfundibular system (see review by Cella, Locatelli and Miiller, 1993). The hypothalamic release of dopamine can be inhibited during a period of stress as a consequence of enhanced release of endogenous opioid peptides (see review by Przewlocki, 1993). This in turn will result in the pituitary secretion of Prl being enhanced when an animal is subjected to stress (Raud, Kiddy and Odell, 1971).…”
Section: Discussionmentioning
confidence: 99%