Cultural advice

The Australian National University acknowledges, celebrates and pays our respects to the Ngunnawal and Ngambri people of the Canberra region and to all First Nations Australians on whose traditional lands we meet and work, and whose cultures are among the oldest continuing cultures in human history.

Aboriginal and Torres Strait Islander peoples are advised that ANU Library collections may include images, names, voices, and other representations of deceased persons.

Material in the collection may contain terms, language or views that reflect the period in which the item was created and may be considered inappropriate today.

Inhibition of passive-avoidance memory formation in the day-old chick by the opioid cytochrophin-4

Loading...
Thumbnail Image

Date

Authors

Freeman, Fiona
Young, I M

Journal Title

Journal ISSN

Volume Title

Publisher

Cold Spring Harbor Laboratory Press

Abstract

Cytochrophin-4 (cyt-4), a tetrapeptide with opioid-like activity, caused amnesia when injected into chick forebrain 5 hr after passive-avoidance training. Bilateral injections of cyt-4 directly into the lobus parolfactorius (LPO) resulted in the chicks being amnesic for the training task 24 hr later, whereas unilateral injections of cyt-4 were effective only when injected into the right LPO. Cyt-4-induced amnesia was reversed by the general opioid antagonist, naloxone, indicating that cyt-4 was acting via an opioid receptor. The μ- and δ-opioid receptors (but not κ-opioid or ORL1-receptors) have been shown to be involved in memory formation 5 hr after training (Freeman and Young 2000). Because an antagonist of the μ-opioid receptor inhibited memory, we attempted to reverse the effect of cyt-4 using μ-opioid receptor agonists. Met[enk] was unable to reverse the inhibition of memory formation by cyt-4 suggesting that the μ-opioid receptor is not involved in this effect. However endomorphin-2 (endo-2) reversed the effect of cyt-4. We further investigated the action of endo-2 using an irreversible antagonist of the μ-receptor, β-funaltrexamine (β-FAN), and found that endo-2 reversed β-FAN-induced amnesia indicating that endo-2 was not acting on the μ-opioid receptor in the chick. Because unilateral injections of β-FAN were not amnesic (bilateral injections were amnesic) this provided further evidence that the effect of cyt-4 was not mediated via the μ-opioid receptor. Coinjection of the δ-receptor agonist, (D-Pen2, L-Pen5)enkephalin (DPLPE), reversed the disruptive effect of cyt-4 on memory. However, memory modulation via the δ-opioid receptor was not lateralized to the right hemisphere suggesting that cyt-4 does not act via this receptor either. It was shown that an antagonist of the ε-opioid receptor inhibited memory at the 5 hr time point. We conclude that the ε-opioid receptor or an unidentified opioid receptor subtype could be involved in the action of cyt-4.

Description

Citation

Source

Learning and Memory

Book Title

Entity type

Access Statement

License Rights

Restricted until

2037-12-31