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A rate-limiting step in antidepressants onset: Excitation of glutamatergic pyramidal neurons in medial prefrontal cortex of rodents.
Yan, Jiao-Zhao; Li, Guang-Xiang; Sun, Si-Rui; Cui, Lin-Yu; Yin, Yong-Yu; Li, Yun-Feng.
Afiliação
  • Yan JZ; Beijing Institute of Basic Medical Sciences, Beijing, China; Beijing Institute of Pharmacology and Toxicology, State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Key Laboratory of Neuropsychopharmacology, Beijing, China.
  • Li GX; Beijing Institute of Basic Medical Sciences, Beijing, China.
  • Sun SR; Beijing Ditan Hospital Capital Medical University, Beijing, China.
  • Cui LY; College of Anesthesia, Shanxi Medical University, Shanxi, China.
  • Yin YY; Beijing Institute of Pharmacology and Toxicology, State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Key Laboratory of Neuropsychopharmacology, Beijing, China. Electronic address: 472586836@qq.com.
  • Li YF; Beijing Institute of Basic Medical Sciences, Beijing, China; Beijing Institute of Pharmacology and Toxicology, State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Key Laboratory of Neuropsychopharmacology, Beijing, China. Electronic address: lyf619@aliyun.com.
Article em En | MEDLINE | ID: mdl-38065287
ABSTRACT
Although clinical antidepressants have varied mechanisms of action, it remains unclear whether they may have a common mechanism underlying their antidepressant effects. We investigated the behavioral effects of five different antidepressants (differing in target, chemical structure, and rate of onset) and their effects on the firing activities of glutamatergic pyramidal neurons in the medial prefrontal cortex (mPFC) using the forced swimming test (FST) and electrophysiological techniques (in vivo). We employed fiber photometry recordings to validate the effects of antidepressants on the firing activity of pyramidal neurons. Additionally, multichannel electrophysiological recordings were conducted in mice exhibiting depressive-like behaviors induced by chronic restraint stress (CRS) to investigate whether antidepressants exert similar effects on pyramidal neurons in depressed mice. Behavioral tests were utilized for evaluating the depression model. We found that fluoxetine, duloxetine, vilazodone, YL-0919, and ketamine all increase the firing activities of glutamatergic pyramidal neurons (at least 57%) while exerting their initial onset of antidepressant effects. Fiber photometry revealed an increase in the calcium activity of pyramidal neurons in the mPFC at the onset of antidepressant effects. Furthermore, a significant reduction was observed in the firing activity of pyramidal neurons in the mPFC of CRS-exposed mice, which was reversed by antidepressants. Taken together, our findings suggested that five pharmacologically distinct classes of antidepressants share the common ability to increase the firing activity of pyramidal neurons, just different time, which might be a rate-limiting step in antidepressants onset. The study contributes to the body of knowledge of the mechanisms underlying antidepressant effects and paves the way for developing rapid-acting antidepressants.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Roedores / Antidepressivos Limite: Animals Idioma: En Revista: Prog Neuropsychopharmacol Biol Psychiatry Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Roedores / Antidepressivos Limite: Animals Idioma: En Revista: Prog Neuropsychopharmacol Biol Psychiatry Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China