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increased calorie intake. TAU promoted increased hypothalamic insulin action only
in CH mice which was linked to prevention of overfeeding, obesity, and glucose
intolerance. Protein-restriction promoted metabolic damages that were not prevented
by TAU supplementation.
Abbreviations
TAU
Taurine
ARC
Arcuate nuclei
T2DM
Type 2 diabetes mellitus
CNS
Central nervous system
ICV
Intracerebroventricular
TNF
Tumor necrosis factor
10.1
Introduction
The hypothalamic Arcuate nuclei (ARC) control feeding behavior and sympathetic/
parasympathetic tones modulating body metabolism (Plum et al.
2006
; Schwartz et al.
2000
). Insulin crosses the blood-brain barrier and binds to its receptor (IR) located in
the ARC. IR activated phosphorylates itself and its substrates (IRS) and leads to phos-
phatidylinositol-3 kinase (PI3K) activation and increased Akt phosphorylation (pAkt)
(Tsai et al. 2003). Central activation of this pathway inhibits the synthesis of orexi-
genic neuropeptides, such as the neuropeptide Y (NPY) and the agouti peptide (AgRP),
and stimulates the secretion of anorexigenic neuropeptides, proopiomelanocortin
(POMC), and the cocaine-and-amphetamine-regulated transcript (CART) (Morton
et al.
2006
; Badman and Flier,
2005
). Therefore, the hypothalamic activation of insu-
lin signaling regulates food intake in order to maintain an adequate body weight.
Obesity is a factor linked to peripheral and central insulin resistance leading to
type 2 diabetes (T2DM) (Kahn et al.
2006
). Impaired central action of insulin in the
obesity results in a vicious circle which provides an increase in weight gain
(Schwartz and Porte
2005
) .
Protein-malnutrition during gestation is a frequent cause of low birth weight, and
is associated with increased susceptibility for developing chronic diseases (Barker
et al.
1993
). Previous reports showed no alteration in IRS1/2 and Akt protein con-
tent in the cerebral cortex from calorie-restricted rats (Mollinedo et al.
2010
) .
Disrupted insulin signaling in the central nervous system (CNS) reflects on food
intake and may link malnutrition in early life and development of T2DM in adult-
hood (Orozco-SolĂs et al.
2010
) .
Taurine (TAU) is a sulfur-containing amino acid present in high concentration in
newborn mice brain. This amino acid is responsible for the maintenance of intracel-
lular osmotic balance (L'Amoreaux et al.
2010
). TAU treatment during mice develop-
ment causes increase of size and number of pancreatic islets without altering exocrine
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