Результаты исследований: Научные публикации в периодических изданиях › Обзорная статья › Рецензирование
Understanding antidepressant discontinuation syndrome (ADS) through preclinical experimental models. / Забегалов, Константин; Колесникова, Татьяна; Хацко, Сергей; Волгин, Андрей; Яковлев, Олег; Амстиславская, Тамара; Алексеева, Полина; Мешалкина, Дарья Андреевна; Friend, Ashton; Bao, Wandong; Демин, Константин Андреевич; Гайнетдинов, Рауль Радикович; Калуев, Алан Валерьевич.
в: European Journal of Pharmacology, Том 829, 15.06.2018, стр. 129-140.Результаты исследований: Научные публикации в периодических изданиях › Обзорная статья › Рецензирование
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TY - JOUR
T1 - Understanding antidepressant discontinuation syndrome (ADS) through preclinical experimental models
AU - Забегалов, Константин
AU - Колесникова, Татьяна
AU - Хацко, Сергей
AU - Волгин, Андрей
AU - Яковлев, Олег
AU - Амстиславская, Тамара
AU - Алексеева, Полина
AU - Мешалкина, Дарья Андреевна
AU - Friend, Ashton
AU - Bao, Wandong
AU - Демин, Константин Андреевич
AU - Гайнетдинов, Рауль Радикович
AU - Калуев, Алан Валерьевич
N1 - Funding Information: The research was supported by the Russian Foundation for Basic Research (RFBR) grant 16-04-00851 to АVK. RRG was supported by a Russian Science Foundation (RSF) grant 14-50-00069. KAD and DAM are supported by the RFBR grants 18-34- 00996 and 18-315-00375, respectively. Appendix A
PY - 2018/6/15
Y1 - 2018/6/15
N2 - Antidepressant drugs are currently one of the most prescribed medications. In addition to treatment resistance and side effects of antidepressants, their clinical use is further complicated by antidepressant discontinuation syndrome (ADS). ADS is a common problem in patients following the interruption, dose reduction, or discontinuation of antidepressant drugs. Clinically, ADS resembles a classical drug withdrawal syndrome, albeit differing from it because antidepressants generally do not induce addiction. The growing clinical importance and prevalence of ADS necessitate novel experimental (animal) models of this disorder. Currently available preclinical models of ADS are mainly rodent-based, and study mostly serotonergic antidepressants and their combinations. Here, we systematically assess clinical ADS symptoms and discuss current trends and challenges in the field of experimental (animal) models of ADS. We also outline basic mechanisms underlying ADS pathobiology, evaluate its genetic, pharmacological and environmental determinants, and emphasize how using animal models may help generate important translational insights into human ADS condition, its prevention and therapy.
AB - Antidepressant drugs are currently one of the most prescribed medications. In addition to treatment resistance and side effects of antidepressants, their clinical use is further complicated by antidepressant discontinuation syndrome (ADS). ADS is a common problem in patients following the interruption, dose reduction, or discontinuation of antidepressant drugs. Clinically, ADS resembles a classical drug withdrawal syndrome, albeit differing from it because antidepressants generally do not induce addiction. The growing clinical importance and prevalence of ADS necessitate novel experimental (animal) models of this disorder. Currently available preclinical models of ADS are mainly rodent-based, and study mostly serotonergic antidepressants and their combinations. Here, we systematically assess clinical ADS symptoms and discuss current trends and challenges in the field of experimental (animal) models of ADS. We also outline basic mechanisms underlying ADS pathobiology, evaluate its genetic, pharmacological and environmental determinants, and emphasize how using animal models may help generate important translational insights into human ADS condition, its prevention and therapy.
KW - Animal models
KW - Antidepressants
KW - Depression
KW - Discontinuation syndrome
KW - Side effects
UR - http://www.scopus.com/inward/record.url?scp=85046350588&partnerID=8YFLogxK
U2 - 10.1016/j.ejphar.2018.04.003
DO - 10.1016/j.ejphar.2018.04.003
M3 - Review article
VL - 829
SP - 129
EP - 140
JO - European Journal of Pharmacology
JF - European Journal of Pharmacology
SN - 0014-2999
ER -
ID: 33277881