@article{70702ed3a8ae4b03b05858f9311bcb90,
title = " Activation of G αq Signaling Enhances Memory Consolidation and Slows Cognitive Decline ",
abstract = " Perhaps the most devastating decline with age is the loss of memory. Therefore, identifying mechanisms to restore memory function with age is critical. Using C. elegans associative learning and memory assays, we identified a gain-of-function G αq signaling pathway mutant that forms a long-term (cAMP response element binding protein [CREB]-dependent) memory following one conditioned stimulus-unconditioned stimulus (CS-US) pairing, which usually requires seven CS-US pairings. Increased CREB activity in AIM interneurons reduces the threshold for memory consolidation through transcription of a set of previously identified “long-term memory” genes. Enhanced G αq signaling in the AWC sensory neuron is both necessary and sufficient for improved memory and increased AIM CREB activity, and activation of G αq specifically in aged animals rescues the ability to form memory. Activation of G αq in AWC sensory neurons non-cell autonomously induces consolidation after one CS-US pairing, enabling both cognitive function maintenance with age and restoration of memory function in animals with impaired memory performance without decreased longevity. Arey et al. have found that activating the G αq signaling pathway in sensory neurons enhances memory in young animals, utilizing the canonical CREB pathway. This pathway also slows age-related memory loss and reverses age-related memory impairment.",
author = "Arey, {Rachel N.} and Stein, {Geneva M.} and Rachel Kaletsky and Amanda Kauffman and Murphy, {Coleen T.}",
note = "Funding Information: We thank J. Ashraf for assistance with the generation of transgenic strains, M. Wright and R. Jin for assistance with behavioral assays, the CGC for strains, and the Murphy lab for valuable discussions. FLP cloning plasmids were a gift from E. Jorgensen. Strains JN897 and JN819 were kind gifts from Y. Iino. IV183 and IV8 were generously provided by S. Chalasani, and CX9735 was a kind gift from C. Bargmann. C.T.M. is the Director of the Paul F. Glenn Center for Biology of Aging Research at Princeton and an HHMI-Simons Faculty Scholar. This work was supported by the NIH (R01AG034446 to C.T.M. and F32AG046106 to R.N.A.). Funding Information: We thank J. Ashraf for assistance with the generation of transgenic strains, M. Wright and R. Jin for assistance with behavioral assays, the CGC for strains, and the Murphy lab for valuable discussions. FLP cloning plasmids were a gift from E. Jorgensen. Strains JN897 and JN819 were kind gifts from Y. Iino. IV183 and IV8 were generously provided by S. Chalasani, and CX9735 was a kind gift from C. Bargmann. C.T.M. is the Director of the Paul F. Glenn Center for Biology of Aging Research at Princeton and an HHMI-Simons Faculty Scholar. This work was supported by the NIH ( R01AG034446 to C.T.M. and F32AG046106 to R.N.A.). Publisher Copyright: {\textcopyright} 2018 Elsevier Inc.",
year = "2018",
month = may,
day = "2",
doi = "10.1016/j.neuron.2018.03.039",
language = "English (US)",
volume = "98",
pages = "562--574.e5",
journal = "Neuron",
issn = "0896-6273",
publisher = "Cell Press",
number = "3",
}