Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
ТРИЦИКЛИЧЕСКИЙ АНТИДЕПРЕССАНТ АМИТРИПТИЛИН ПОДАВЛЯЕТ Са2+-ОТВЕТЫ В ПЕРИТОНЕАЛЬНЫХ МАКРОФАГАХ КРЫСЫ. / Миленина, Лидия Сергеевна; Крутецкая, Зоя Иринарховна; Антонов, Виктор Георгиевич; Крутецкая, Нина Иринарховна.
в: Цитология, Том 66, № 2, 15.03.2024, стр. 161-172.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - ТРИЦИКЛИЧЕСКИЙ АНТИДЕПРЕССАНТ АМИТРИПТИЛИН ПОДАВЛЯЕТ Са2+-ОТВЕТЫ В ПЕРИТОНЕАЛЬНЫХ МАКРОФАГАХ КРЫСЫ
AU - Миленина, Лидия Сергеевна
AU - Крутецкая, Зоя Иринарховна
AU - Антонов, Виктор Георгиевич
AU - Крутецкая, Нина Иринарховна
N1 - Миленина Л.С., Крутецкая З.И., Антонов В.Г., Крутецкая Н.И. ТРИЦИКЛИЧЕСКИЙ АНТИДЕПРЕССАНТ АМИТРИПТИЛИН ПОДАВЛЯЕТ Са2+-ОТВЕТЫ В ПЕРИТОНЕАЛЬНЫХ МАКРОФАГАХ КРЫСЫ. ЦИТОЛОГИЯ. 2024. Т. 66. № 2. С. 161-172.
PY - 2024/3/15
Y1 - 2024/3/15
N2 - Amitriptyline is a tricyclic antidepressant widely used in clinical practice for the treatment of anxiety, depression and chronic pain. These drugs have a multifaceted effect on cellular processes. One of their targets is sigma-1 receptors. Sigma-1 receptors are molecular chaperones located in endoplasmic reticulum membrane; they are characterized by a unique structure and pharmacological profile. Sigma-1 receptors regulate many cellular processes in health and disease, including Ca2+ signaling. Using Fura-2AM microfluorimetry, it was shown for the first time that sigma-1 receptor agonist, antidepressant amitriptyline, significantly suppresses both Ca2+ mobilization from intracellular Ca2+-stores and subsequent store-dependent Ca2+ entry into cells, induced by endoplasmic Ca2+-ATPase inhibitors thapsigargin and cyclopiazonic acid, as well as disulfide-containing immunomodulators glutoxim and molixan, in rat peritoneal macrophages. The results suggest the involvement of sigma-1 receptors in a complex signaling cascade induced by glutoxim or molixan, leading to an increase of intracellular Ca2+ concentration in macrophages. The results also indicate the participation of sigma-1 receptors in the regulation of store-dependent Ca2+ entry in macrophages.
AB - Amitriptyline is a tricyclic antidepressant widely used in clinical practice for the treatment of anxiety, depression and chronic pain. These drugs have a multifaceted effect on cellular processes. One of their targets is sigma-1 receptors. Sigma-1 receptors are molecular chaperones located in endoplasmic reticulum membrane; they are characterized by a unique structure and pharmacological profile. Sigma-1 receptors regulate many cellular processes in health and disease, including Ca2+ signaling. Using Fura-2AM microfluorimetry, it was shown for the first time that sigma-1 receptor agonist, antidepressant amitriptyline, significantly suppresses both Ca2+ mobilization from intracellular Ca2+-stores and subsequent store-dependent Ca2+ entry into cells, induced by endoplasmic Ca2+-ATPase inhibitors thapsigargin and cyclopiazonic acid, as well as disulfide-containing immunomodulators glutoxim and molixan, in rat peritoneal macrophages. The results suggest the involvement of sigma-1 receptors in a complex signaling cascade induced by glutoxim or molixan, leading to an increase of intracellular Ca2+ concentration in macrophages. The results also indicate the participation of sigma-1 receptors in the regulation of store-dependent Ca2+ entry in macrophages.
UR - https://www.mendeley.com/catalogue/5a257400-d48e-3098-89af-ceec16368408/
U2 - 10.31857/S0041377124020069
DO - 10.31857/S0041377124020069
M3 - статья
VL - 66
SP - 161
EP - 172
JO - Цитология
JF - Цитология
SN - 0041-3771
IS - 2
ER -
ID: 125930465