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Researchers at Baylor College of Medicine, the University of Cambridge within the U.Ok. and collaborating establishments have proven that serotonin 2C receptor within the mind regulates reminiscence in folks and animal fashions. The findings, printed within the journal Science Advances, not solely present new insights into the components concerned in wholesome reminiscence but additionally in circumstances related to reminiscence loss, like Alzheimer’s illness, and counsel novel avenues for therapy.
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“Serotonin, a compound produced by neurons within the midbrain, acts as a neurotransmitter, passing messages between mind cells,” mentioned co-corresponding creator Dr. Yong Xu, professor of pediatrics – diet and affiliate director for primary sciences at the USDA/ARS Children’s Nutrition Research Center at Baylor. “Serotonin-producing neurons attain out to a number of mind areas together with the hippocampus, a area important for short- and long-term reminiscence.”
Serotonin communicates messages to mind cells by binding to receptors on the cell floor, which cue the receiving cell to hold on a sure exercise. On this research, the Xu lab, with experience in genetic animal research, and the human genetics lab of co-corresponding creator Dr. I. Sadaf Farooqi, professor of metabolism and medication on the College of Cambridge, targeted on serotonin 2C receptors, that are abundantly current within the mind’s ventral hippocampal CA1 area (vCA1), investigating the function of the receptor in reminiscence in people and animal fashions.
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“We had beforehand recognized 5 people carrying variants of the serotonin 2C receptor gene (HTR2C) that produce faulty types of the receptor,” Farooqi mentioned. “Folks with these uncommon variants confirmed important deficits on reminiscence questionnaires. These findings led us to research the affiliation between HTR2C variants and reminiscence deficits in animal fashions.”
The crew genetically engineered mice to imitate the human mutation. When the researchers ran behavioral checks on these mice to judge their reminiscence, they discovered that each women and men with the non-functional gene confirmed decreased reminiscence recall in comparison with the unmodified animals. “After we mixed the human information and the mouse information, we discovered compelling proof connecting non-functional mutations of the serotonin receptor 2C with reminiscence deficits in people,” Xu mentioned.
The animal fashions additionally enabled the crew to dig deeper into how the receptor mediates reminiscence. They found a mind circuit that begins within the midbrain the place serotonin-producing neurons are positioned. These neurons mission to the vCA1 area, which has ample serotonin 2C receptors. “When neurons within the midbrain reaching out to neurons within the vCA1 area launch serotonin, the neurotransmitter binds to its receptor signaling these cells to make modifications that assist the mind consolidate reminiscences,” Xu mentioned.
Importantly, the researchers additionally discovered that this serotonin-associated neural circuit is broken in a mouse mannequin of Alzheimer’s illness. “The neural circuit within the Alzheimer’s illness animal mannequin doesn’t launch ample serotonin into the vCA1 area to sign the modifications required to consolidate a reminiscence,” Xu mentioned.
Nonetheless, it’s doable to bypass this lack of serotonin and instantly activate the downstream serotonin receptor by administering a serotonin analog, lorcaserin, a compound that selectively prompts the serotonin 2C receptor in these cells. “We examined this technique in our animal mannequin and had been excited to seek out that the animals handled with the serotonin analog improved their reminiscence,” Xu mentioned. “We hope our findings encourage additional research to judge the worth of serotonin analogs within the therapy of Alzheimer’s illness.”
Different contributors to this work embrace Hesong Liu, Yang He, Hailan Liu, Bas Brouwers, Na Yin, Katherine Lawler, Julia M. Keogh, Elana Henning, Dong-Kee Lee, Meng Yu, Longlong Tu, Nan Zhang, Kristine M. Conde, Junying Han, Zili Yan, Nikolas A. Scarcelli, Lan Liao, Jianming Xu, Qingchun Tong, Hui Zheng, Zheng Solar, Yongjie Yang, Chunmei Wang and Yanlin He. The authors are affiliated with one of many following establishments: Baylor School of Drugs, Texas Kids’s Hospital, College of Cambridge, College of Texas Well being Science Heart at Houston and Louisiana State College.
See the publication for the sources of monetary help for this work.
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