Результаты исследований: Научные публикации в периодических изданиях › Обзорная статья › Рецензирование
The Role of TRP Channels in Sepsis and Colitis. / Дворникова, Кристина Алексеевна; Платонова, Ольга Николаевна; Быстрова, Елена Юрьевна.
в: International Journal of Molecular Sciences, Том 25, № 9, 4784, 27.04.2024.Результаты исследований: Научные публикации в периодических изданиях › Обзорная статья › Рецензирование
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TY - JOUR
T1 - The Role of TRP Channels in Sepsis and Colitis
AU - Дворникова, Кристина Алексеевна
AU - Платонова, Ольга Николаевна
AU - Быстрова, Елена Юрьевна
PY - 2024/4/27
Y1 - 2024/4/27
N2 - To date, several members of the transient receptor potential (TRP) channels which provide a wide array of roles have been found in the gastrointestinal tract (GI). The goal of earlier research was to comprehend the intricate signaling cascades that contribute to TRP channel activation as well as how these receptors' activity affects other systems. Moreover, there is a large volume of published studies describing the role of TRP channels in a number of pathological disorders, including inflammatory bowel disease (IBD) and sepsis. Nevertheless, the generalizability of these results is subject to certain limitations. For instance, the study of IBD relies on various animal models and experimental methods, which are unable to precisely imitate the multifactorial chronic disease. The diverse pathophysiological mechanisms and unique susceptibility of animals may account for the inconsistency of the experimental data collected. The main purpose of this study was to conduct a comprehensive review and analysis of existing studies on transient receptor potential (TRP) channels implicating specific models of colitis and sepsis, with particular emphasis on their involvement in pathological disorders such as IBD and sepsis. Furthermore, the text endeavors to evaluate the generalizability of experimental findings, taking into consideration the limitations posed by animal models and experimental methodologies. Finally, we also provide an updated schematic of the most important and possible molecular signaling pathways associated with TRP channels in IBD and sepsis.
AB - To date, several members of the transient receptor potential (TRP) channels which provide a wide array of roles have been found in the gastrointestinal tract (GI). The goal of earlier research was to comprehend the intricate signaling cascades that contribute to TRP channel activation as well as how these receptors' activity affects other systems. Moreover, there is a large volume of published studies describing the role of TRP channels in a number of pathological disorders, including inflammatory bowel disease (IBD) and sepsis. Nevertheless, the generalizability of these results is subject to certain limitations. For instance, the study of IBD relies on various animal models and experimental methods, which are unable to precisely imitate the multifactorial chronic disease. The diverse pathophysiological mechanisms and unique susceptibility of animals may account for the inconsistency of the experimental data collected. The main purpose of this study was to conduct a comprehensive review and analysis of existing studies on transient receptor potential (TRP) channels implicating specific models of colitis and sepsis, with particular emphasis on their involvement in pathological disorders such as IBD and sepsis. Furthermore, the text endeavors to evaluate the generalizability of experimental findings, taking into consideration the limitations posed by animal models and experimental methodologies. Finally, we also provide an updated schematic of the most important and possible molecular signaling pathways associated with TRP channels in IBD and sepsis.
KW - Animals
KW - Colitis/metabolism
KW - Disease Models, Animal
KW - Humans
KW - Inflammatory Bowel Diseases/metabolism
KW - Sepsis/metabolism
KW - Signal Transduction
KW - Transient Receptor Potential Channels/metabolism
KW - colitis
KW - intestine
KW - CLP
KW - LPS
KW - TRP channels
KW - inflammatory bowel disease
KW - endotoxins
KW - inflammation
KW - ulcerative colitis
KW - sepsis
KW - Crohn’s disease
UR - https://www.mendeley.com/catalogue/cad5cb24-3735-38f6-8057-f70a7ed6ac84/
U2 - 10.3390/ijms25094784
DO - 10.3390/ijms25094784
M3 - Review article
C2 - 38731999
VL - 25
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
SN - 1422-0067
IS - 9
M1 - 4784
ER -
ID: 119490035