TY - JOUR
T1 - Stress induced analgesia
T2 - its opioid nature depends on the strain of rat but not on the mode of induction
AU - Urca, Gideon
AU - Segev, Shlomo
AU - Sarne, Yosef
N1 - Funding Information:
We thank Endo Labs for their generous supply of naloxone. This study was supported by a grant from the Israel Academy of Sciences and a grant from the Israeli Ministry of Health to G.U. and Y.S.
PY - 1985/9/23
Y1 - 1985/9/23
N2 - Reports by several investigators have shown that both opioid and non-opioid analgesia can be induced by non-pharmacological manipulations such as the administration of electric shock, and that such analgesia depends on shock parameters, the affective state of the animal and the region of the body shocked. We tested several manipulations which have been reported to induced opioid analgesia using a local strain of rats (CR). Such manipulations included the used of 30 min of intermittent footshock (3 mA, 1 s on, 5 s off), brief shock to the forepaws, transpineal electroconvulsive shock (ECS) and tail shock induced helplessness. Administration of either naloxone or naltrexone to rats of the CR strain failed to attenuate the analgesic effect of these manipulations and in some cases even enhanced analgesia. The existence of functional opioid analgesia systems in CR rats was evident from the fact that electrical stimulation of the periaqueductal gray area produced naloxone sensitive analgesia. In additional experiments we compared the analgesic effect of brief continuous (3 min) footshock, prolonged intermittent footshock (30 min) and ECS in young (< 75 days of age) and old (> 75 days of age) rats of the Sabra strain. Young Sabra rats showed naloxone sensitive analgesia following all 3 manipulations while adult rats displayed analgesia which was naloxone insensitive. Furthermore, no decrement in learning, indicative of helplessness, could be demonstrated in young Sabras following 3 min of shock which induced naloxone sensitive analgesia. We therefore propose that both opioid and non-opioid analgesia systems are coactivated by external stressors independent of the mode of stress or the indication of helplessness and that the determinants of their expression are genetically and ontogenetically determined.
AB - Reports by several investigators have shown that both opioid and non-opioid analgesia can be induced by non-pharmacological manipulations such as the administration of electric shock, and that such analgesia depends on shock parameters, the affective state of the animal and the region of the body shocked. We tested several manipulations which have been reported to induced opioid analgesia using a local strain of rats (CR). Such manipulations included the used of 30 min of intermittent footshock (3 mA, 1 s on, 5 s off), brief shock to the forepaws, transpineal electroconvulsive shock (ECS) and tail shock induced helplessness. Administration of either naloxone or naltrexone to rats of the CR strain failed to attenuate the analgesic effect of these manipulations and in some cases even enhanced analgesia. The existence of functional opioid analgesia systems in CR rats was evident from the fact that electrical stimulation of the periaqueductal gray area produced naloxone sensitive analgesia. In additional experiments we compared the analgesic effect of brief continuous (3 min) footshock, prolonged intermittent footshock (30 min) and ECS in young (< 75 days of age) and old (> 75 days of age) rats of the Sabra strain. Young Sabra rats showed naloxone sensitive analgesia following all 3 manipulations while adult rats displayed analgesia which was naloxone insensitive. Furthermore, no decrement in learning, indicative of helplessness, could be demonstrated in young Sabras following 3 min of shock which induced naloxone sensitive analgesia. We therefore propose that both opioid and non-opioid analgesia systems are coactivated by external stressors independent of the mode of stress or the indication of helplessness and that the determinants of their expression are genetically and ontogenetically determined.
KW - analgesia
KW - electroconvulsive shock analgesia
KW - endorphin
KW - opiate
KW - rat
KW - stress-induced analgesia
UR - http://www.scopus.com/inward/record.url?scp=0022367230&partnerID=8YFLogxK
U2 - 10.1016/0006-8993(85)90737-1
DO - 10.1016/0006-8993(85)90737-1
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AN - SCOPUS:0022367230
SN - 0006-8993
VL - 343
SP - 216
EP - 222
JO - Brain Research
JF - Brain Research
IS - 2
ER -