“…Reasoning in the same line, the second experiment was designed to establish differences in analgesia levels by pharmacological manipulations, whereas stress intensity (i.e., 50 bites) was kept constant. Because on the one hand social conflict analgesia, induced by high number of bites, can be influenced by opioid antagonists (Miczek et al, 1982; Rodgers & Hendrie, 1983; Rodgers & Randall, 1985; Siegfried, Frischknecht, Külling, & Waser, 1986; Teskey et al, 1984) and, on the other hand, the LTA reaction of rats is reduced when naltrexone is administered before the 80 inescapable tailshocks (Maier et al, 1980), we presumed that injections of opioid antagonists before the stress of 50 bites should prevent the LTA reaction. The opioid antagonists that we chose were naloxone, a short-acting antagonist, and beta-chlornaltrexamine, known for its long-acting potency by irreversible binding to opioid receptors (Frischknecht, Siegfried, Riggio, & Waser, 1983; Portoghese, Larson, Jiang, Caruso, & Takemori, 1979).…”