Learning and Memory 1986
DOI: 10.1016/b978-0-08-034186-6.50053-0
|View full text |Cite
|
Sign up to set email alerts
|

Defeat-induced Analgesia and the Conditioned Display of Submissive Postures and Escape in Strains of Mice

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
3
0

Year Published

1987
1987
1987
1987

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(3 citation statements)
references
References 13 publications
0
3
0
Order By: Relevance
“…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).…”
Section: Experiments 2: Antagonism Of Social Conflict Analgesia and Ltamentioning
confidence: 99%
See 2 more Smart Citations
“…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).…”
Section: Experiments 2: Antagonism Of Social Conflict Analgesia and Ltamentioning
confidence: 99%
“…For instance, brief exposure to attack elicits a low-intensity, naloxone-insensitive analgesia that dissipates within 10 min (Rodgers & Randall, 1986; Siegfried, Frischknecht, Riggio, & Waser, 1987) and does not show cross-tolerance to or from morphine (Rodgers & Randall, 1986). In contrast, a prolonged exposure to attack induces a long-lasting analgesia that can be reversed by opioid antagonists (Miczek et al, 1982; Miczek, Thompson, & Shuster, 1985; Rodgers & Hendrie, 1983; Rodgers & Randall, 1985; Siegfried, Frischknecht, Külling, & Waser, 1986; Teskey et al, 1984), displays full cross-tolerance with morphine (Miczek et al, 1982; Rodgers & Randall, 1985), and is accompanied by changes in the endogenous opioid systems (Miczek & Thompson, 1984; Raab, Seizinger, & Herz, 1985).…”
mentioning
confidence: 99%
See 1 more Smart Citation