Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2000-6-13
pubmed:abstractText
Two-photon excitation microscopy was used to image and quantify NAD(P)H autofluorescence from intact pancreatic islets under glucose stimulation. At maximal glucose stimulation, the rise in whole-cell NAD(P)H levels was estimated to be approximately 30 microM. However, because glucose-stimulated insulin secretion involves both glycolytic and Kreb's cycle metabolism, islets were cultured on extracellular matrix that promotes cell spreading and allows spatial resolution of the NAD(P)H signals from the cytoplasm and mitochondria. The metabolic responses in these two compartments are shown to be differentially stimulated by various nutrient applications. The glucose-stimulated increase of NAD(P)H fluorescence within the cytoplasmic domain is estimated to be approximately 7 microM. Likewise, the NAD(P)H increase of the mitochondrial domain is approximately 60 microM and is delayed with respect to the change in cytoplasmic NAD(P)H by approximately 20 sec. The large mitochondrial change in glucose-stimulated NAD(P)H thus dominates the total signal but may depend on the smaller but more rapid cytoplasmic increase.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-10506984, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-10506992, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-10733993, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-13575447, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-13890836, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-2943567, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-3110211, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-37138, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-391551, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-4201956, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-4395441, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-6769728, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-7574498, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-8086, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-8157622, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-8363584, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-8631975, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-8645138, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-8720129, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-8824267, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-8962467, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-9013600, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-9115730, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-9534004, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-9746543, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-9825692, http://linkedlifedata.com/resource/pubmed/commentcorrection/10792038-9974390
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0027-8424
pubmed:author
pubmed:issnType
Print
pubmed:day
9
pubmed:volume
97
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
5203-7
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
2000
pubmed:articleTitle
Separation of the glucose-stimulated cytoplasmic and mitochondrial NAD(P)H responses in pancreatic islet beta cells.
pubmed:affiliation
Department of Molecular Physiology and Biophysics, 702 Light Hall, Vanderbilt University, Nashville, TN 37232, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S.