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1.
Int J Biol Macromol ; 268(Pt 1): 131741, 2024 May.
Artículo en Inglés | MEDLINE | ID: mdl-38649083

RESUMEN

Glycogen, a complex branched glucose polymer, is responsible for sugar storage in blood glucose homeostasis. It comprises small ß particles bound together into composite α particles. In diabetic livers, α particles are fragile, breaking apart into smaller particles in dimethyl sulfoxide, DMSO; they are however stable in glycogen from healthy animals. We postulate that the bond between ß particles in α particles involves hydrogen bonding. Liver-glycogen fragility in normal and db/db mice (an animal model for diabetes) is compared using various hydrogen-bond breakers (DMSO, guanidine and urea) at different temperatures. The results showed different degrees of α-particle disruption. Disrupted glycogen showed changes in the mid-infra-red spectrum that are related to hydrogen bonds. While glycogen α-particles are only fragile under harsh, non-physiological conditions, these results nevertheless imply that the bonding between ß particles in α particles is different in diabetic livers compared to healthy, and is probably associated with hydrogen bonding.


Asunto(s)
Enlace de Hidrógeno , Animales , Ratones , Dimetilsulfóxido/química , Glucógeno Hepático/metabolismo , Urea/química , Guanidina/química , Guanidina/farmacología , Hígado/metabolismo , Masculino
2.
Carbohydr Polym ; 237: 116144, 2020 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-32241436

RESUMEN

Liver glycogen, a highly branched glucose polymer, is important for blood sugar homeostasis. It comprises α particles which are made of linked ß particles; the molecular structure changes diurnally. In diabetic liver, the α particles are fragile, easily breaking apart into ß particles in chaotropic agents such as dimethyl sulfoxide. We here use size-exclusion chromatography to study how fasting changes liver-glycogen structure in vivo for mice in which type-2 diabetes had previously been induced. Diabetic glycogen degraded enzymatically more quickly in the fasted animals than did glycogen without fasting, with fewer α particles, which however were still fragile. The glycogen had fewer long chains and more shorter chains after fasting. This study gives an overview of the in vivo dynamic changes in α-particles under starvation conditions in both normal and diabetic livers.


Asunto(s)
Diabetes Mellitus Experimental/metabolismo , Diabetes Mellitus Tipo 2/metabolismo , Ayuno , Glucógeno Hepático/química , Animales , Cromatografía en Gel , Glucógeno Hepático/metabolismo , Masculino , Ratas Sprague-Dawley
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