Alterations in pharmacological and behavioural responses in recombinant mouse line with an increased predisposition to catalepsy: role of the 5‐HT1A receptor

• Published in: British journal of pharmacology 2016-07, Vol.173 (13), p.2147-2161
• Main Authors: Kulikova, E A, Bazovkina, D V, Akulov, A E, Tsybko, A S, Fursenko, D V, Kulikov, A V, Naumenko, V S, Ponimaskin, E, Kondaurova, E M
• Format: Article
• Language: English
• Subjects: 8-Hydroxy-2-(di-n-propylamino)tetralin - pharmacology; Animals; Catalepsy - drug therapy; Catalepsy - genetics; Catalepsy - metabolism; Catalepsy - psychology; Male; Mice; Mice, Inbred C57BL; Mice, Inbred CBA; Mice, Transgenic; Receptor, Serotonin, 5-HT1A - genetics; Receptor, Serotonin, 5-HT1A - metabolism; Research Paper; Rodents; Themed Section: Research Papers
• ISSN: 0007-1188; 1476-5381
• DOI: 10.1111/bph.13484

Background and Purpose One important syndrome of psychiatric disorders in humans is catalepsy. Here, we created mice with different predispositions to catalepsy and analysed their pharmacological and behavioural properties. Experimental Approach Two mouse lines, B6‐M76C and B6‐M76B, were created by transfer of the main locus of catalepsy containing the 5‐HT1A receptor gene to the C57BL/6 genetic background. Behaviour, brain morphology, expression of key components of the serotoninergic system, and pharmacological responses to acute and chronic stimulation of the 5‐HT1A receptor were compared. Key Results B6‐M76B mice were not cataleptic, whereas 14% of B6‐M76C mice demonstrated catalepsy and decreased depressive‐like behaviour. Acute administration of the 5‐HT1A receptor agonist 8‐OH‐DPAT resulted in dose‐dependent hypothermia and in decreased locomotion in both lines. Chronic 8‐OH‐DPAT administration abolished the 5‐HT1A receptor‐mediated hypothermic response in B6‐M76C mice and increased locomotor activity in B6‐M76B mice. In addition, 5‐HT metabolism was significantly reduced in the hippocampus of B6‐M76C mice, and this effect was accompanied by an increased expression of the 5‐HT1A receptor. Conclusions and Implications Our findings indicate that transfer of the main locus of hereditary catalepsy containing the 5‐HT1A receptor from CBA mice to the C57BL/6 genetic background led to increased postsynaptic and decreased presynaptic functional responses of the 5‐HT1A receptor. This characteristic establishes the B6‐M76C line as an attractive model for the pharmacological screening of 5‐HT1A receptor‐related drugs specifically acting on either pre‐ or postsynaptic receptors. Linked Articles This article is part of a themed section on Updating Neuropathology and Neuropharmacology of Monoaminergic Systems. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v173.13/issuetoc