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The possible role of medial prefrontal cortex beta-1-adrenoceptors in morphine-induced amnesia
Anahita Torkaman-Boutorabi1, Seyed-Milad Hashemi-Hezaveh, Hadi Sheidadoust
1Department of Neuroscience, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Abstract:
The prelimbic region of the medial prefrontal cortex (mPFC) in the brain is crucial for memory. Norepinephrine elicits an important influence on mPFC functions. The stimulation of β-adrenoceptors (β-ARs) may play a critical role in the consolidation of long-term memory. The present study examines the possible role of β₁-ARs located in the mPFC on morphine-induced amnesia in rats. The animals were bilaterally implanted with chronic cannulas in the mPFC, trained in a step-through-type passive avoidance task and tested 24 h after training to measure step-through latency. Our present results indicated that posttraining intraperitoneal administration of morphine (2.5, 5 and 7.5 mg/kg) dose-dependently reduced the step-through latency. Different doses of xamoterol (0.01, 0.1 and 1 µg/rat) have shown no significant change in the step-through latency, but posttraining intra-mPFC microinjection of atenolol (0.2 and 0.4 µg/rat) had an amnesic effect. Moreover, atenolol-caused amnesia was reversed by an ineffective dose of xamoterol (0.1 µg/rat). On the other hand, coadministration of an ineffective dose of atenolol (0.1 µg/rat) with an ineffective dose of morphine (2.5 mg/kg) induced an amnesic effect. Meanwhile, xamoterol had no effect on morphine-induced amnesia. These results suggest that β₁-ARs of the prelimbic region in the mPFC may play an important role in morphine-induced amnesia.
Insights
Beta-1 adrenoceptors (β₁-ARs) in the medial prefrontal cortex (mPFC) are involved in morphine-induced amnesia. Blocking these receptors with atenolol caused memory impairment, suggesting their role in memory consolidation.
Area of Science:
- Neuroscience
- Pharmacology
- Memory Research
Background:
- The medial prefrontal cortex (mPFC) is vital for memory functions.
- Norepinephrine and β-adrenoceptors (β-ARs) significantly influence mPFC activity.
- β-AR stimulation is implicated in long-term memory consolidation.
Purpose of the Study:
- To investigate the role of β₁-ARs in the mPFC on morphine-induced amnesia in rats.
- To determine if β₁-ARs in the prelimbic region of the mPFC are involved in memory impairment caused by morphine.
Main Methods:
- Rats were implanted with cannulas in the mPFC.
- A step-through passive avoidance task was used to assess memory.
- Morphine, xamoterol (a β₁-AR agonist), and atenolol (a β₁-AR antagonist) were administered post-training.
Main Results:
- Morphine administration dose-dependently impaired memory (reduced step-through latency).
- Atenolol, a β₁-AR antagonist, induced amnesia when microinjected into the mPFC.
- Xamoterol reversed atenolol-induced amnesia, but did not affect morphine-induced amnesia.
- Combined ineffective doses of atenolol and morphine produced amnesia.
Conclusions:
- β₁-ARs in the prelimbic region of the mPFC play a significant role in morphine-induced amnesia.
- These findings highlight the involvement of specific β-adrenoceptor subtypes in the mPFC in drug-induced memory deficits.
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