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Role of neuronal nicotinic acetylcholine receptors (nAChRs) on learning and memory in zebrafish.
Psychopharmacology (Berl). 2014 May; 231(9):1975-85.P

Abstract

RATIONALE

Neuronal nicotinic acetylcholine receptors (nAChRs) play a modulatory role in cognition, and zebrafish provide a preclinical model to study learning and memory.

OBJECTIVES

We investigated the effect of nicotine (NIC) and some new cytisine-derived partial agonists (CC4 and CC26) on spatial memory in zebrafish using a rapid assay on T-maze task. The role of α4/α6β2 and the α7 nAChRs in NIC-induced memory enhancement was evaluated using selective nAChR antagonists.

RESULTS

Low and high doses of NIC, cytisine (CYT), CC4 and CC26 respectively improved and worsened the mean running time, showing an inverted U dose-response function. The effective dose (ED50) (×10⁻⁵ mg/kg) was 0.4 for CC4, 4.5 for CYT, 140 for NIC and 200 for CC26. NIC-induced cognitive enhancement was reduced by the selective nAChR subtype antagonists: methyllycaconitine (MLA) for α7, α-conotoxin (MII) for α6β2, dihydro-β-erythroidine (DhβE) for α4β2, the nonselective antagonist mecamylamine (MEC) and the muscarinic antagonist scopolamine (SCOP), with DhβE being more active than MLA or MII. All the partial agonists blocked the cognitive enhancement. The improvement with the maximal active dose of each partial agonist was blocked by low doses of DhβE (0.001 mg/kg) and MII (0.01 mg/kg). MLA reduced the effects of CC26 and CC4 at doses of 0.01 and 1 mg/kg, respectively, but did not antagonize CYT-induced memory improvement at any of the tested dose. No change in swimming activity was observed.

CONCLUSIONS

Our findings demonstrate that zebrafish make a useful model for the rapid screening of the effect of new α4β2 nAChR compounds on spatial memory.

Authors+Show Affiliations

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale, Università degli Studi di Milano, Milan, Italy.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

24311357

Citation

Braida, Daniela, et al. "Role of Neuronal Nicotinic Acetylcholine Receptors (nAChRs) On Learning and Memory in Zebrafish." Psychopharmacology, vol. 231, no. 9, 2014, pp. 1975-85.
Braida D, Ponzoni L, Martucci R, et al. Role of neuronal nicotinic acetylcholine receptors (nAChRs) on learning and memory in zebrafish. Psychopharmacology (Berl). 2014;231(9):1975-85.
Braida, D., Ponzoni, L., Martucci, R., Sparatore, F., Gotti, C., & Sala, M. (2014). Role of neuronal nicotinic acetylcholine receptors (nAChRs) on learning and memory in zebrafish. Psychopharmacology, 231(9), 1975-85. https://doi.org/10.1007/s00213-013-3340-1
Braida D, et al. Role of Neuronal Nicotinic Acetylcholine Receptors (nAChRs) On Learning and Memory in Zebrafish. Psychopharmacology (Berl). 2014;231(9):1975-85. PubMed PMID: 24311357.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Role of neuronal nicotinic acetylcholine receptors (nAChRs) on learning and memory in zebrafish. AU - Braida,Daniela, AU - Ponzoni,Luisa, AU - Martucci,Roberta, AU - Sparatore,Fabio, AU - Gotti,Cecilia, AU - Sala,Mariaelvina, Y1 - 2013/12/06/ PY - 2013/07/18/received PY - 2013/10/14/accepted PY - 2013/12/7/entrez PY - 2013/12/7/pubmed PY - 2014/12/15/medline SP - 1975 EP - 85 JF - Psychopharmacology JO - Psychopharmacology (Berl.) VL - 231 IS - 9 N2 - RATIONALE: Neuronal nicotinic acetylcholine receptors (nAChRs) play a modulatory role in cognition, and zebrafish provide a preclinical model to study learning and memory. OBJECTIVES: We investigated the effect of nicotine (NIC) and some new cytisine-derived partial agonists (CC4 and CC26) on spatial memory in zebrafish using a rapid assay on T-maze task. The role of α4/α6β2 and the α7 nAChRs in NIC-induced memory enhancement was evaluated using selective nAChR antagonists. RESULTS: Low and high doses of NIC, cytisine (CYT), CC4 and CC26 respectively improved and worsened the mean running time, showing an inverted U dose-response function. The effective dose (ED50) (×10⁻⁵ mg/kg) was 0.4 for CC4, 4.5 for CYT, 140 for NIC and 200 for CC26. NIC-induced cognitive enhancement was reduced by the selective nAChR subtype antagonists: methyllycaconitine (MLA) for α7, α-conotoxin (MII) for α6β2, dihydro-β-erythroidine (DhβE) for α4β2, the nonselective antagonist mecamylamine (MEC) and the muscarinic antagonist scopolamine (SCOP), with DhβE being more active than MLA or MII. All the partial agonists blocked the cognitive enhancement. The improvement with the maximal active dose of each partial agonist was blocked by low doses of DhβE (0.001 mg/kg) and MII (0.01 mg/kg). MLA reduced the effects of CC26 and CC4 at doses of 0.01 and 1 mg/kg, respectively, but did not antagonize CYT-induced memory improvement at any of the tested dose. No change in swimming activity was observed. CONCLUSIONS: Our findings demonstrate that zebrafish make a useful model for the rapid screening of the effect of new α4β2 nAChR compounds on spatial memory. SN - 1432-2072 UR - https://www.unboundmedicine.com/medline/citation/24311357/Role_of_neuronal_nicotinic_acetylcholine_receptors__nAChRs__on_learning_and_memory_in_zebrafish_ L2 - https://dx.doi.org/10.1007/s00213-013-3340-1 DB - PRIME DP - Unbound Medicine ER -