Glycogen metabolism is impaired in the brain of male type 2 diabetic Goto-Kakizaki rats
Soares, Ana Francisca LU ; Nissen, Jakob D ; Garcia-Serrano, Alba M ; Nussbaum, Sakura S ; Waagepetersen, Helle S and Duarte, João M N LU
(2019)
In Journal of Neuroscience Research
97(8).
p.1004-1017
- Abstract
Diabetes impacts the central nervous system predisposing to cognitive decline. While glucose is the main source of energy fueling the adult brain, brain glycogen is necessary for adequate neuronal function, synaptic plasticity and memory. In this study, we tested the hypothesis that brain glycogen metabolism is impaired in type 2 diabetes (T2D). 13 C magnetic resonance spectroscopy (MRS) during [1-13 C]glucose i.v. infusion was employed to detect 13 C incorporation into whole-brain glycogen in male Goto-Kakizaki (GK) rats, a lean model of T2D, and control Wistar rats. Labeling from [1-13 C]glucose into brain glycogen occurred at a rate of 0.25 ± 0.12 and 0.48 ± 0.22 µmol/g/h in GK and Wistar rats, respectively (p = 0.028), despite... (More)
Diabetes impacts the central nervous system predisposing to cognitive decline. While glucose is the main source of energy fueling the adult brain, brain glycogen is necessary for adequate neuronal function, synaptic plasticity and memory. In this study, we tested the hypothesis that brain glycogen metabolism is impaired in type 2 diabetes (T2D). 13 C magnetic resonance spectroscopy (MRS) during [1-13 C]glucose i.v. infusion was employed to detect 13 C incorporation into whole-brain glycogen in male Goto-Kakizaki (GK) rats, a lean model of T2D, and control Wistar rats. Labeling from [1-13 C]glucose into brain glycogen occurred at a rate of 0.25 ± 0.12 and 0.48 ± 0.22 µmol/g/h in GK and Wistar rats, respectively (p = 0.028), despite similar brain glycogen concentrations. In addition, the appearance of [1-13 C]glucose in the brain was used to evaluate glucose transport and consumption. T2D caused a 31% reduction (p = 0.031) of the apparent maximum transport rate (Tmax ) and a tendency for reduced cerebral metabolic rate of glucose (CMRglc ; -29%, p = 0.062), indicating impaired glucose utilization in T2D. After MRS in vivo, gas chromatography-mass spectrometry was employed to measure regional 13 C fractional enrichment of glucose and glycogen in the cortex, hippocampus, striatum, and hypothalamus. The diabetes-induced reduction in glycogen labeling was most prominent in the hippocampus and hypothalamus, which are crucial for memory and energy homeostasis, respectively. These findings were further supported by changes in the phosphorylation rate of glycogen synthase, as analyzed by Western blotting. Altogether, the present results indicate that T2D is associated with impaired brain glycogen metabolism.
(Less)
- author
- Soares, Ana Francisca
LU
; Nissen, Jakob D
; Garcia-Serrano, Alba M
; Nussbaum, Sakura S
; Waagepetersen, Helle S
and Duarte, João M N
LU
- organization
- publishing date
- 2019-05-01
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Journal of Neuroscience Research
- volume
- 97
- issue
- 8
- pages
- 1004 - 1017
- publisher
- John Wiley & Sons Inc.
- external identifiers
-
- pmid:31044444
- scopus:85065245191
- ISSN
- 1097-4547
- DOI
- 10.1002/jnr.24437
- language
- English
- LU publication?
- yes
- additional info
- © 2019 Wiley Periodicals, Inc.
- id
- 0c7d497c-df05-4a37-ae67-d9b6e0fd358c
- date added to LUP
- 2019-05-16 08:41:33
- date last changed
- 2024-03-03 07:06:06
@article{0c7d497c-df05-4a37-ae67-d9b6e0fd358c,
abstract = {{<p>Diabetes impacts the central nervous system predisposing to cognitive decline. While glucose is the main source of energy fueling the adult brain, brain glycogen is necessary for adequate neuronal function, synaptic plasticity and memory. In this study, we tested the hypothesis that brain glycogen metabolism is impaired in type 2 diabetes (T2D). 13 C magnetic resonance spectroscopy (MRS) during [1-13 C]glucose i.v. infusion was employed to detect 13 C incorporation into whole-brain glycogen in male Goto-Kakizaki (GK) rats, a lean model of T2D, and control Wistar rats. Labeling from [1-13 C]glucose into brain glycogen occurred at a rate of 0.25 ± 0.12 and 0.48 ± 0.22 µmol/g/h in GK and Wistar rats, respectively (p = 0.028), despite similar brain glycogen concentrations. In addition, the appearance of [1-13 C]glucose in the brain was used to evaluate glucose transport and consumption. T2D caused a 31% reduction (p = 0.031) of the apparent maximum transport rate (Tmax ) and a tendency for reduced cerebral metabolic rate of glucose (CMRglc ; -29%, p = 0.062), indicating impaired glucose utilization in T2D. After MRS in vivo, gas chromatography-mass spectrometry was employed to measure regional 13 C fractional enrichment of glucose and glycogen in the cortex, hippocampus, striatum, and hypothalamus. The diabetes-induced reduction in glycogen labeling was most prominent in the hippocampus and hypothalamus, which are crucial for memory and energy homeostasis, respectively. These findings were further supported by changes in the phosphorylation rate of glycogen synthase, as analyzed by Western blotting. Altogether, the present results indicate that T2D is associated with impaired brain glycogen metabolism.</p>}},
author = {{Soares, Ana Francisca and Nissen, Jakob D and Garcia-Serrano, Alba M and Nussbaum, Sakura S and Waagepetersen, Helle S and Duarte, João M N}},
issn = {{1097-4547}},
language = {{eng}},
month = {{05}},
number = {{8}},
pages = {{1004--1017}},
publisher = {{John Wiley & Sons Inc.}},
series = {{Journal of Neuroscience Research}},
title = {{Glycogen metabolism is impaired in the brain of male type 2 diabetic Goto-Kakizaki rats}},
url = {{http://dx.doi.org/10.1002/jnr.24437}},
doi = {{10.1002/jnr.24437}},
volume = {{97}},
year = {{2019}},
}