Volume 22, Issue 1 (4-2019)                   J Arak Uni Med Sci 2019, 22(1): 73-84 | Back to browse issues page

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Rahimi Tesiye M, Valizadegan F, Oryan S. Interaction between Effects of Opioidergic System of Prefrontal Cortex and Dopaminergic System of Basolateral Amygdala in Working Memory. J Arak Uni Med Sci 2019; 22 (1) :73-84
URL: http://jams.arakmu.ac.ir/article-1-5858-en.html
1- Department of Biology, Faculty of Basic Sciences, University of Mazandaran, Babolsar, Iran. , maryamrahimi563@yahoo.com
2- Department of Biology, Faculty of Basic Sciences, University of Mazandaran, Babolsar, Iran.
3- Department of Animal Sciences, Faculty of Biological Sciences, Kharazmi University, Tehran, Iran.
Abstract:   (2965 Views)
Background and Aim: Working memory is a dynamic neural system for temporarily maintaining and processing of information. Prefrontal cortex (PFC) is the main processing center of Working memory by using different neurotransmitter systems communicate with other brain structures such as Basolateral Amygdala (BLA). In this study, we investigated the role of Opioidergic system in medial PFC and Dopaminergic system of BLA nucleus in working memory based on RAM test.
Materials and Methods: In this study, The male Wistar rats were used. Rats were cannulated with stereotaxic surgery in mPFC and BLA sites. After a recovery period, they were microinjected. Parameters such as working and reference memory errors were calculated with DSWS protocol.
Ethical Considerations: This study with research ethics code IR.UMZ.REC.1397.23 has been approved by Bioethics Committee at Mazandaran University, Iran.
Findings: High doses of Morphine (2 µg/rat) intra mPFC and Chloropromazine (2 µg/rat) intra BLA have improving effects on working and reference memory (p≤0.05). Low (0.005 µg/rat) and high dose (0.5 µg/rat) of Apomorphine had improving {(p≤0.05), (p≤0.01)} and the moderate dose (0.05 µg/rat) of it had decreasing effect on working and reference memory (p≤0.01). Microinjection of Morphine (0.5 µg/rat) with triple doses of Chloropromazine had no significant change on working and reference memory errors. Interaction of Morphine (0.5 µg/rat) with different doses of Apomorphine could change Apomorphine different effects. Coadministration of different doses of Apomorphine with effective dose of Chloropromazine (2 µg/rat) and Morphine (2 µg/rat) decreased the working and reference memory errors.
Conclusion: Our findings showed that in processing of working and reference memory, opioidergic system in mPFC and dopaminergic system in BLA, are interacting reciprocally.
Full-Text [PDF 595 kb]   (860 Downloads)    
Type of Study: Original Atricle | Subject: Basic Sciences
Received: 2018/07/19 | Accepted: 2018/12/16

References
1. Baddeley A. The episodic buffer: a new component of working memory?. Trends in cognitive sciences. 2000; 4(11): 417-423.
2. Honig WK. Studies of working memory in the pigeon. In Cognitive processes in animal behavior. 2018; 211-248.
3. Basar-Eroglu C, Brand A, Hildebrandt H, Kedzior KK, Mathes B, Schmiedt C. Working memory related gamma oscillations in schizophrenia patients. International Journal of Psychophysiology. 2007; 64(1): 39-45.
4. Holstege G, Georgiadis JR, Paans AM, Meiners LC, Van Der Graaf FH, Reinders AS. Brain activation during human male ejaculation. Journal of Neuroscience. 2003; 23(27): 9185-9193.
5. Sherman SM, Guillery RW. The role of the thalamus in the flow of information to the cortex. Philosophical Transactions of the Royal Society of London B: Biological Sciences. 2002; 357(1428): 1695-1708.
6. Takahashi H, Yamada M, Suhara T. Functional significance of central D1 receptors in cognition: beyond working memory. Journal of Cerebral Blood Flow & Metabolism. 2012; 32(7): 1248-1258.
7. Gallagher M, Holland PC. The amygdala complex: multiple roles in associative learning and attention. Proceedings of the National Academy of Sciences. 1994; 91(25): 11771-11776.
8. Rezayof A, Darbandi N, Zarrindast M-R. Nicotinic acetylcholine receptors of the ventral tegmental area are involved in mediating morphine-state-dependent learning. Neurobiology of learning and memory. 2008; 90(1): 255-60.
9. Shin IC, Kim HC, Swanson J, Hong JT, Oh KW. Anxiolytic effects of acute morphine can be modulated by nitric oxide systems. Pharmacology. 2003; 68(4): 183-189.
10. Phillips AG, Ahn S, Floresco SB. Magnitude of dopamine release in medial prefrontal cortex predicts accuracy of memory on a delayed response task. Journal of Neuroscience. 2004; 24(2): 547-553.
11. Kelley AE, Domesick VB, Nauta WJH. The amygdalostriatal projection in the rat an anatomical study by anterograde and retrograde tracing methods. In Neuroanatomy. 1982; 495-509.
12. Wang JH, Rizak JD, Chen YM, Li L, Hu XT, Ma YY. Interactive effects of morphine and dopaminergic compounds on spatial working memory in rhesus monkeys. Neuroscience bulletin. 2013; 29(1): 37-46.
13. Watanabe Y, Funahashi S. Thalamic mediodorsal nucleus and working memory. Neuroscience & Biobehavioral. 2012; 36(1): 134-142.
14. Shiigi Y, Takahashi M, Kaneto H. Facilitation of memory retrieval by pretest morphine mediated by μ but not δ and κ opioid receptors. Psychopharmacology. 1990; 102(3): 329-332.
15. Homayoun H, Khavandgar S & Zarrindast MR. Morphine state-dependent learning: interactions with α2-adrenoceptors and acute stress. Behavioural pharmacology. 2003; 14(1): 41-48.
16. Almasi-Nasrabadi M, Javadi-Paydar M, Mahdavian S, Babaei R, Sharifian M, Norouzi A, et al. Involvement of NMDA receptors in the beneficial effects of pioglitazone on scopolamine-induced memory impairment in mice. Behavioural brain research. 2012; 231(1): 138-45.
17. Del Arco A, Mora F. Neurotransmitters and prefrontal cortex–limbic system interactions: implications for plasticity and psychiatric disorders. Journal of neural transmission. 2009; 116(8): 941-952.
18. Gabbott PL, Warner TA, Jays PR, Salway P, Busby SJ. Prefrontal cortex in the rat: projections to subcortical autonomic, motor, and limbic centers. Journal of Comparative Neurology. 2005; 492(2): 145-177.
19. Sesack SR, Grace AA. Cortico-basal ganglia reward network. microcircuitry. Neuropsychopharmacology. 2010; 35(1): 27.
20. Jackson ME, MoghaddamB. Amygdala regulation of nucleus accumbens dopamine output is governed by the prefrontal cortex. Journal of neuroscience. 2001; 21(2): 676-681.
21. Li Z, Wu CF, Pei G, Xu NJ. Reversal of morphine-induced memory impairment in mice by withdrawal in Morris water maze: possible involvement of cholinergic system. Pharmacology Biochemistry and Behavior. 2001; 68(3): 507-513.
22. Kroner S, Rosenkranz JA, Grace AA & Barrionuevo G. Dopamine modulates excitability of basolateral amygdala neurons in vitro. Journal of neurophysiology. 2005; 93(3): 1598-1610.
23. Shulz DE, Sosnik R, Ego V, Haidarliu S & Ahissar E. A neuronal analogue of state-dependent learning. Nature. 2000; 403(6769): 549-553.
24. Koob GF, Volkow ND. Neurocircuitry of addiction. Neuropsychopharmacology. 2010; 35: 217–238.
25. Dash PK, Moore, AN, Kobori N & Runyan JD. Molecular activity underlying working memory. Learning & memory. 2007; 14(8): 554-563.
26. Hill DR & Bowery NG. 3H-baclofen and 3H-GABA bind to bicuculline-insensitive GABAB sites in rat brain. Nature. 1981; 290(5802):149-152.
27. Pisani F, Oteri G, Costa C, Di Raimondo G & Di Perri R. Effects of psychotropic drugs on seizure threshold. Drug Safety. 2002; 25(2): 91-110.
28. Runyan JD, Moore AN, Dash PK, A role for prefrontal calcium-sensitive protein phosphatase and kinase activities in working memory. Learn. Mem. 2005; 12:103-110.
29. Leucht C, Kitzmantel M, Kane J, Leucht S, Chua WL. Haloperidol versus chlorpromazine for schizophrenia. Cochrane Database of Systematic Reviews. 2008 (1).
30. Valizadegan F & Rahimi Tesiye M. Evaluation of D1 and D2 dopamine receptors families’ role in basolateral amygdala on working and reference memory. 2018; Nova Biologica Rep. 5: 53- 64.

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