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dc.date.accessioned | 2019-11-05T13:07:13Z | |
dc.date.available | 2019-11-05T13:07:13Z | |
dc.date.issued | 2001 | |
dc.identifier.uri | http://sedici.unlp.edu.ar/handle/10915/84894 | |
dc.description.abstract | We correlated the changes in glucose-induced insulin secretion with those observed in glucose metabolism and hexokinase/glucokinase activity in islets from normal sucrose-fed hamsters. Blood glucose and insulin levels were measured in normal male hamsters fed with (S5) or without (C5) 10% sucrose in the drinking water for 5 weeks. Isolated islets (collagenase digestion) from both groups of animals were used to study insulin secretion, 14CO2 and 3H2O production from D-[U-14C]-glucose and D-[5-3H]-glucose respectively, with 3.3 or 16.7 mM glucose in the medium, and hexokinase/glucokinase activity (fluorometric assay) in islet homogenates. Whereas S5 and C5 animals had comparable normal blood glucose levels, S5 showed higher insulin levels than C5 hamsters (2.3 ± 0.1 vs 0.6 ± 0.03 ng/ml, P<0.001). Islets from S5 hamsters released significantly more insulin than C5 islets in the presence of low and high glucose (3.3 mM glucose: 0.77 ± 0.04 vs 0.20 ± 0.06 pg/ng DNA/min, P<0.001; 16.7 mM glucose: 2.77 ± 0.12 vs 0.85 ± 0.06 pg/ng DNA/min, P<0.001) and produced significantly higher amounts of 14CO2 and 3H2O at both glucose concentrations (14CO2: 3.3 mM glucose: 0.27 ± 0.01 vs 0.18 ± 0.01, P<0.001; 16.7 mM glucose: 1.44 ± 0.15 vs 0.96 ± 0.08, P<0.02; 3H2O: 3.3 mM glucose: 0.31 ± 0.02 vs 0.15 ± 0.01, P<0.001; 16.7 mM glucose: 1.46 ± 0.20 vs 0.76 ± 0.05 pmol glucose/ng DNA/min, P<0.005). The hexokinase Km and Vmax values from S5 animals were significantly higher than those from C5 ones (Km: 100.14 ± 7.01 vs 59.90 ± 3.95 ♂M, P<0.001; Vmax: 0.010 ± 0.0005 vs 0.008 ± 0.0006 pmol glucose/ng DNA/min, P<0.02). Conversely, the glucokinase Km value from S5 animals was significantly lower than in C5 animals (Km: 15.31 ± 2.64 vs 35.01 ± 1.65 mM, P<0.001), whereas Vmax figures were within a comparable range in both groups (Vmax: 0.048 ± 0.009 vs 0.094 ± 0.035 pmol glucose/ng DNA/min, not significant). The glucose phosphorylation ratio measured at 1 and 100 mM (hexokinase/glucokinase ratio) was significantly higher in S5 (0.26 ± 0.02) than in C5 animals (0.11 ± 0.01, P<0.005), and it was attributable to an increase in the hexokinase activity in S5 animals. In conclusion, sucrose administration increased the hexokinase/glucokinase activity ratio in the islets, which would condition the increase in glucose metabolism by β-cells, and in β-cell sensitivity and responsiveness to glucose. These results support the concept that increased hexokinase rather than glucokinase activity causes the β-cell hypersensitivity to glucose, hexokinase being metabolically more active than glucokinase to up-regulate β-cell function. | en |
dc.format.extent | 551-556 | es |
dc.language | en | es |
dc.subject | sucrose administration | es |
dc.subject | pancreatic islets | es |
dc.subject | β-cells | es |
dc.title | Changes induced by sucrose administration on glucose metabolism in pancreatic islets in normal hamsters | en |
dc.type | Articulo | es |
sedici.identifier.other | doi:10.1677/joe.0.1710551 | es |
sedici.identifier.other | eid:2-s2.0-0035664153 | es |
sedici.identifier.issn | 0022-0795 | es |
sedici.creator.person | Massa, María Laura | es |
sedici.creator.person | Borelli, María Inés | es |
sedici.creator.person | Del Zotto, Héctor Herminio | es |
sedici.creator.person | Gagliardino, Juan José | es |
sedici.subject.materias | Ciencias Médicas | es |
sedici.description.fulltext | true | es |
mods.originInfo.place | Facultad de Ciencias Médicas | es |
mods.originInfo.place | Centro de Endocrinología Experimental y Aplicada | es |
sedici.subtype | Articulo | es |
sedici.rights.license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) | |
sedici.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | |
sedici.description.peerReview | peer-review | es |
sedici.relation.journalTitle | Journal of Endocrinology | es |
sedici.relation.journalVolumeAndIssue | vol. 171, no. 3 | es |
sedici.rights.sherpa | * RoMEO: amarillo* Pre-print del autor: can* Post-print del autor: restricted* Versión de editor/PDF:cannot* Condiciones:>>On Institutional repository or Central repository>>La versión de editor/PDF no puede utilizarse>>La declaración establecida debe acompañar el depósito (ver Política)>>El pre-print no debe reemplazarse por el post-print, sino que se enlazará a la versión publicada con una declaración establecida corregida>>El editor depositará copia en PubMed Central en nombre de los autores financiados por el NIH>>Publisher last contacted on 06/06/2019* Link a Sherpa: http://sherpa.ac.uk/romeo/issn/0022-0795/es/ |