Matches in SemOpenAlex for { <https://semopenalex.org/work/W3162178502> ?p ?o ?g. }
- W3162178502 endingPage "e1009002" @default.
- W3162178502 startingPage "e1009002" @default.
- W3162178502 abstract "NMDA receptors promote repolarization in pancreatic beta cells and thereby reduce glucose-stimulated insulin secretion. Therefore, NMDA receptors are a potential therapeutic target for diabetes. While the mechanism of NMDA receptor inhibition in beta cells is rather well understood at the molecular level, its possible effects on the collective cellular activity have not been addressed to date, even though proper insulin secretion patterns result from well-synchronized beta cell behavior. The latter is enabled by strong intercellular connectivity, which governs propagating calcium waves across the islets and makes the heterogeneous beta cell population work in synchrony. Since a disrupted collective activity is an important and possibly early contributor to impaired insulin secretion and glucose intolerance, it is of utmost importance to understand possible effects of NMDA receptor inhibition on beta cell functional connectivity. To address this issue, we combined confocal functional multicellular calcium imaging in mouse tissue slices with network science approaches. Our results revealed that NMDA receptor inhibition increases, synchronizes, and stabilizes beta cell activity without affecting the velocity or size of calcium waves. To explore intercellular interactions more precisely, we made use of the multilayer network formalism by regarding each calcium wave as an individual network layer, with weighted directed connections portraying the intercellular propagation. NMDA receptor inhibition stabilized both the role of wave initiators and the course of waves. The findings obtained with the experimental antagonist of NMDA receptors, MK-801, were additionally validated with dextrorphan, the active metabolite of the approved drug dextromethorphan, as well as with experiments on NMDA receptor KO mice. In sum, our results provide additional and new evidence for a possible role of NMDA receptor inhibition in treatment of type 2 diabetes and introduce the multilayer network paradigm as a general strategy to examine effects of drugs on connectivity in multicellular systems." @default.
- W3162178502 created "2021-05-24" @default.
- W3162178502 creator A5000033283 @default.
- W3162178502 creator A5025238651 @default.
- W3162178502 creator A5030041504 @default.
- W3162178502 creator A5044886935 @default.
- W3162178502 creator A5071867549 @default.
- W3162178502 creator A5072210204 @default.
- W3162178502 creator A5073579013 @default.
- W3162178502 date "2021-05-11" @default.
- W3162178502 modified "2023-10-17" @default.
- W3162178502 title "NMDA receptor inhibition increases, synchronizes, and stabilizes the collective pancreatic beta cell activity: Insights through multilayer network analysis" @default.
- W3162178502 cites W1528873260 @default.
- W3162178502 cites W1537358164 @default.
- W3162178502 cites W1552235434 @default.
- W3162178502 cites W1554796897 @default.
- W3162178502 cites W1690684669 @default.
- W3162178502 cites W1832397049 @default.
- W3162178502 cites W1914535897 @default.
- W3162178502 cites W1964988818 @default.
- W3162178502 cites W1966556202 @default.
- W3162178502 cites W1966587178 @default.
- W3162178502 cites W1969359749 @default.
- W3162178502 cites W1972811274 @default.
- W3162178502 cites W1973533455 @default.
- W3162178502 cites W1976255517 @default.
- W3162178502 cites W1986597140 @default.
- W3162178502 cites W1995056605 @default.
- W3162178502 cites W1995915018 @default.
- W3162178502 cites W2002157354 @default.
- W3162178502 cites W2010387488 @default.
- W3162178502 cites W2011588834 @default.
- W3162178502 cites W2014716037 @default.
- W3162178502 cites W2017509811 @default.
- W3162178502 cites W2017801522 @default.
- W3162178502 cites W2019077674 @default.
- W3162178502 cites W2024057780 @default.
- W3162178502 cites W2024380057 @default.
- W3162178502 cites W2028467165 @default.
- W3162178502 cites W2028686926 @default.
- W3162178502 cites W2030689510 @default.
- W3162178502 cites W2031558550 @default.
- W3162178502 cites W2036441475 @default.
- W3162178502 cites W2042317260 @default.
- W3162178502 cites W2055599620 @default.
- W3162178502 cites W2062783006 @default.
- W3162178502 cites W2065171939 @default.
- W3162178502 cites W2065285024 @default.
- W3162178502 cites W2066885602 @default.
- W3162178502 cites W2068782608 @default.
- W3162178502 cites W2068892782 @default.
- W3162178502 cites W2073682155 @default.
- W3162178502 cites W2080940048 @default.
- W3162178502 cites W2084572092 @default.
- W3162178502 cites W2084957552 @default.
- W3162178502 cites W2085568467 @default.
- W3162178502 cites W2090971379 @default.
- W3162178502 cites W2094657730 @default.
- W3162178502 cites W2104417933 @default.
- W3162178502 cites W2104762573 @default.
- W3162178502 cites W2108585459 @default.
- W3162178502 cites W2108896758 @default.
- W3162178502 cites W2110809248 @default.
- W3162178502 cites W2113303890 @default.
- W3162178502 cites W2116424238 @default.
- W3162178502 cites W2123936091 @default.
- W3162178502 cites W2127982470 @default.
- W3162178502 cites W2131042436 @default.
- W3162178502 cites W2131129193 @default.
- W3162178502 cites W2139828787 @default.
- W3162178502 cites W2140402299 @default.
- W3162178502 cites W2147387884 @default.
- W3162178502 cites W2153956170 @default.
- W3162178502 cites W2154712565 @default.
- W3162178502 cites W2160109462 @default.
- W3162178502 cites W2160401579 @default.
- W3162178502 cites W2164698356 @default.
- W3162178502 cites W2164983923 @default.
- W3162178502 cites W2168500187 @default.
- W3162178502 cites W2168676771 @default.
- W3162178502 cites W2171361408 @default.
- W3162178502 cites W2171601942 @default.
- W3162178502 cites W2211746017 @default.
- W3162178502 cites W2258402864 @default.
- W3162178502 cites W2336446961 @default.
- W3162178502 cites W2359561706 @default.
- W3162178502 cites W2442470680 @default.
- W3162178502 cites W2465180814 @default.
- W3162178502 cites W2474710707 @default.
- W3162178502 cites W2498257067 @default.
- W3162178502 cites W2516174717 @default.
- W3162178502 cites W2543536036 @default.
- W3162178502 cites W2592529564 @default.
- W3162178502 cites W2610797963 @default.
- W3162178502 cites W2622190181 @default.
- W3162178502 cites W2724625730 @default.
- W3162178502 cites W2741748366 @default.
- W3162178502 cites W2742312725 @default.