» Articles » PMID: 19320932

Alpha-ketoglutarate Protects the Liver of Piglets Exposed During Prenatal Life to Chronic Excess of Dexamethasone from Metabolic and Structural Changes

Overview
Date 2009 Mar 27
PMID 19320932
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Glucocorticoids play a role in the origin of the features of the metabolic diseases. Alpha-ketoglutarate (AKG) is defined as glutamine homologue and derivative, conditionally an essential amino acid. In the liver, glutamine serves as a precursor for ureagenesis, gluconeogenesis and acute phase protein synthesis The aim of the study was to determine the effect of AKG administered to piglets prenatally exposed to dexamethasone, on the structure of the liver and its metabolic function. Sows were administered with dexamethasone (3 mg/sow/48 h) from day 70 of pregnancy to the parturition, and then after the birth, the piglets were divided into the group administered with AKG (0.4 g/kg body weight) or physiological saline. Biochemical markers, lysozyme and ceruloplasmin serum activities, concentrations of selected free amino acids, macro- and microelements and histomorphometry of the liver tissue were determined. The total cholesterol concentrations in the sows and their newborns from the Dex groups were higher by 72% and 64%, respectively, compared with the control groups. Triacylglycerol concentration was higher by 50% in sows from the Dex group and 55% in the new-born piglets. Alpha-ketoglutarate administered to the piglets after prenatal influence of dexamethasone lowered the total cholesterol concentration by 40%, and enhanced aspartate by 41%, serine by 76%, glutamate by 105%, glutamine by 36%, glycine by 53% and arginine by 105%, as well as methionine and cystathionine, but increased the sulphur concentration compared with the control (p < 0.01). Intracellular space D decreased after AKG administration in comparison with the piglets from Dex/Control group not treated with AKG. Postnatal administration of AKG had a protective effect on liver structure, and lowered the total cholesterol concentration in piglets prenatally exposed to dexamethasone, and also influenced selected macro- and microelement serum concentrations and amino acids plasma concentration.

Citing Articles

Prenatal Fumonisin Exposure Impairs Bone Development via Disturbances in the OC/Leptin and RANKL/RANK/OPG Systems in Weaned Rat Offspring.

Tomaszewska E, Rudyk H, Muszynski S, Hulas-Stasiak M, Leszczynski N, Mielnik-Blaszczak M Int J Mol Sci. 2023; 24(10).

PMID: 37240089 PMC: 10217822. DOI: 10.3390/ijms24108743.


Basal Intestinal Morphology, Immunolocalization of Leptin and Ghrelin and Their Receptors in Newborn Wistar Rats after Prenatal Exposure to Fumonisins.

Tomaszewska E, Rudyk H, Dobrowolski P, Arciszewski M, Donaldson J, Kras K Animals (Basel). 2023; 13(9).

PMID: 37174575 PMC: 10177403. DOI: 10.3390/ani13091538.


Regulatory T cell differentiation is controlled by αKG-induced alterations in mitochondrial metabolism and lipid homeostasis.

Matias M, Yong C, Foroushani A, Goldsmith C, Mongellaz C, Sezgin E Cell Rep. 2021; 37(5):109911.

PMID: 34731632 PMC: 10167917. DOI: 10.1016/j.celrep.2021.109911.


The Effects of Prenatal Supplementation with β-Hydroxy-β-Methylbutyrate and/or Alpha-Ketoglutaric Acid on the Development and Maturation of Mink Intestines Are Dependent on the Number of Pregnancies and the Sex of the Offspring.

Dobrowolski P, Muszynski S, Donaldson J, Jakubczak A, Zmuda A, Taszkun I Animals (Basel). 2021; 11(5).

PMID: 34065327 PMC: 8160670. DOI: 10.3390/ani11051468.


The Protective Role of Alpha-Ketoglutaric Acid on the Growth and Bone Development of Experimentally Induced Perinatal Growth-Retarded Piglets.

Tomaszewska E, Burmanczuk N, Dobrowolski P, Swiatkiewicz M, Donaldson J, Burmanczuk A Animals (Basel). 2021; 11(1).

PMID: 33435211 PMC: 7826854. DOI: 10.3390/ani11010137.