Matches in SemOpenAlex for { <https://semopenalex.org/work/W2100556265> ?p ?o ?g. }
- W2100556265 endingPage "370" @default.
- W2100556265 startingPage "353" @default.
- W2100556265 abstract "The expression of ATP-sensitive K(+) (K(ATP)) channels by magnocellular cholinergic basal forebrain (BF) neurones was investigated in thin brain slice and dissociated cell culture preparations using a combination of whole-cell, perforated-patch and single-channel recording techniques. Greater than 95% of BF neurones expressed functional K(ATP) channels whose activation resulted in membrane hyperpolarization and a profound fall in excitability. The whole-cell K(ATP) conductance was 14.0 +/- 1.5 nS and had a reversal potential of -91.4 +/- 0.9 mV that shifted by 59.6 mV with a tenfold increase in [K(+)](o). I(KATP) was inhibited reversibly by tolbutamide (IC(50) of 34.1 microM) and irreversibly by glibenclamide (0.3-3 nM) and had a low affinity for [ATP](i) (67% reduction with 6 mm[MgATP](i)). Using perforated-patch recording, a small proportion of the conductance was found to be tonically active. This was weakly potentiated by diazoxide (0.1 mm extracellular glucose) but insensitive to pinacidil (< or =500 microM). Single-channel K(ATP) currents recorded in symmetrical 140 mm K(+)-containing solutions exhibited weak inward rectification with a mean conductance of 66.2 +/- 1.9 pS. Channel activity was inhibited by MgATP (>50 microM) and activated by MgADP (200 microM). The K(+) channels opener diazoxide (200-500 microM) increased channel opening probability (NP(o)) by 486 +/- 120% whereas pinacidil (500 microM) had no effect. In conclusion, the characteristics of the K(ATP) channels expressed by BF neurones are very similar to channels composed of SUR1 and Kir6.2 subunits. In the native cell, their affinity for ATP is close to the resting [ATP](i), potentially allowing them to be modulated by physiologically relevant changes in [ATP](i). The effect of these channels on the level of ascending cholinergic excitation of the cortex and hippocampus is discussed." @default.
- W2100556265 created "2016-06-24" @default.
- W2100556265 creator A5017799110 @default.
- W2100556265 creator A5027714194 @default.
- W2100556265 date "2004-01-01" @default.
- W2100556265 modified "2023-10-18" @default.
- W2100556265 title "Modulation of the excitability of cholinergic basal forebrain neurones by K<sub>ATP</sub> channels" @default.
- W2100556265 cites W1487837909 @default.
- W2100556265 cites W1496028330 @default.
- W2100556265 cites W1517407659 @default.
- W2100556265 cites W1556708911 @default.
- W2100556265 cites W1966756523 @default.
- W2100556265 cites W1982817785 @default.
- W2100556265 cites W1983011541 @default.
- W2100556265 cites W1986962364 @default.
- W2100556265 cites W1991864133 @default.
- W2100556265 cites W1993464225 @default.
- W2100556265 cites W1995269134 @default.
- W2100556265 cites W1995589371 @default.
- W2100556265 cites W1999698913 @default.
- W2100556265 cites W2001418258 @default.
- W2100556265 cites W2003567871 @default.
- W2100556265 cites W2003976073 @default.
- W2100556265 cites W2010320641 @default.
- W2100556265 cites W2017531990 @default.
- W2100556265 cites W2022324525 @default.
- W2100556265 cites W2030890979 @default.
- W2100556265 cites W2032897738 @default.
- W2100556265 cites W2033069335 @default.
- W2100556265 cites W2033657502 @default.
- W2100556265 cites W2044165578 @default.
- W2100556265 cites W2044612428 @default.
- W2100556265 cites W2045267269 @default.
- W2100556265 cites W2045815714 @default.
- W2100556265 cites W2048268426 @default.
- W2100556265 cites W2050342883 @default.
- W2100556265 cites W2058530714 @default.
- W2100556265 cites W2060884581 @default.
- W2100556265 cites W2060964837 @default.
- W2100556265 cites W2061854524 @default.
- W2100556265 cites W2065428236 @default.
- W2100556265 cites W2066650398 @default.
- W2100556265 cites W2068401152 @default.
- W2100556265 cites W2073097841 @default.
- W2100556265 cites W2073653273 @default.
- W2100556265 cites W2074306054 @default.
- W2100556265 cites W2076203907 @default.
- W2100556265 cites W2078526156 @default.
- W2100556265 cites W2080455120 @default.
- W2100556265 cites W2082004277 @default.
- W2100556265 cites W2082648108 @default.
- W2100556265 cites W2083379786 @default.
- W2100556265 cites W2083584165 @default.
- W2100556265 cites W2094099923 @default.
- W2100556265 cites W2094858856 @default.
- W2100556265 cites W2107862591 @default.
- W2100556265 cites W2113460545 @default.
- W2100556265 cites W2147706045 @default.
- W2100556265 cites W2148047353 @default.
- W2100556265 cites W2148255642 @default.
- W2100556265 cites W2154147755 @default.
- W2100556265 cites W2160119775 @default.
- W2100556265 cites W2166610424 @default.
- W2100556265 cites W2168503470 @default.
- W2100556265 cites W2168552101 @default.
- W2100556265 cites W2172211138 @default.
- W2100556265 cites W2417574325 @default.
- W2100556265 cites W2067514674 @default.
- W2100556265 doi "https://doi.org/10.1113/jphysiol.2003.055889" @default.
- W2100556265 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1664773" @default.
- W2100556265 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/14578474" @default.
- W2100556265 hasPublicationYear "2004" @default.
- W2100556265 type Work @default.
- W2100556265 sameAs 2100556265 @default.
- W2100556265 citedByCount "65" @default.
- W2100556265 countsByYear W21005562652012 @default.
- W2100556265 countsByYear W21005562652013 @default.
- W2100556265 countsByYear W21005562652015 @default.
- W2100556265 countsByYear W21005562652017 @default.
- W2100556265 countsByYear W21005562652018 @default.
- W2100556265 countsByYear W21005562652019 @default.
- W2100556265 countsByYear W21005562652020 @default.
- W2100556265 countsByYear W21005562652021 @default.
- W2100556265 countsByYear W21005562652022 @default.
- W2100556265 countsByYear W21005562652023 @default.
- W2100556265 crossrefType "journal-article" @default.
- W2100556265 hasAuthorship W2100556265A5017799110 @default.
- W2100556265 hasAuthorship W2100556265A5027714194 @default.
- W2100556265 hasBestOaLocation W21005562651 @default.
- W2100556265 hasConcept C114614502 @default.
- W2100556265 hasConcept C121932024 @default.
- W2100556265 hasConcept C12554922 @default.
- W2100556265 hasConcept C131453863 @default.
- W2100556265 hasConcept C134018914 @default.
- W2100556265 hasConcept C147944092 @default.
- W2100556265 hasConcept C170493617 @default.
- W2100556265 hasConcept C181911157 @default.
- W2100556265 hasConcept C185592680 @default.