Journal
JOURNAL OF PHARMACOLOGICAL SCIENCES
Volume 148, Issue 4, Pages 364-368Publisher
JAPANESE PHARMACOLOGICAL SOC
DOI: 10.1016/j.jphs.2022.02.006
Keywords
Galantamine; Social interaction; Cholecystokinin receptor transgenic mice
Categories
Funding
- Japan Society for the Promotion of Science [15K08218, 16K10195, 17H04252]
- Private University Research Branding Project Grant from the Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT)
- Meijo Research Institute
- Meijo Asian Research Center
- Takeda Science Foundation
- Nakatomi Foundation
- Smoking Research Foundation
- Grants-in-Aid for Scientific Research [15K08218, 16K10195] Funding Source: KAKEN
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In this study, the researchers found that galantamine improved social interaction impairments, but failed to attenuate anxiety-like behavior. This effect was mediated by alpha 7 nAChR and blocked by an alpha 7 nAChR antagonist, methyllycaconitine.
We examined whether galantamine (GAL), a cholinesterase inhibitor and allosteric potentiating ligand for alpha 7 nicotinic acetylcholine receptor (nAChR), had an impact on emotional abnormalities in forebrain-specific cholecystokinin receptor-2 overexpressed transgenic mice. Treatment with GAL (1 mg/kg, s.c.) attenuated the decrease of social interaction time, but failed to attenuate anxiety-like behavior in the elevated plus-maze test. The effect of GAL was blocked by an alpha 7 nAChR antagonist, methyllycaconitine (3 mg/kg, i.p.). These results suggest that GAL improved social interaction impairments via alpha 7 nAChR and could be useful to treat sociability-related emotional abnormalities. (C) 2022 The Authors. Production and hosting by Elsevier B.V. on behalf of Japanese Pharmacological Society.
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