» Articles » PMID: 15352999

Glucose-stimulated Insulin Response in Pregnant Sheep Following Acute Suppression of Plasma Non-esterified Fatty Acid Concentrations

Overview
Publisher Biomed Central
Date 2004 Sep 9
PMID 15352999
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Elevated non-esterified fatty acids (NEFA) concentrations in non-pregnant animals have been reported to decrease pancreatic responsiveness. As ovine gestation advances, maternal insulin concentrations fall and NEFA concentrations increase. Experiments were designed to examine if the pregnancy-associated rise in NEFA concentration is associated with a reduced pancreatic sensitivity to glucose in vivo. We investigated the possible relationship of NEFA concentrations in regulating maternal insulin concentrations during ovine pregnancy at three physiological states, non-pregnant, non-lactating (NPNL), 105 and 135 days gestational age (dGA, term 147+/- 3 days).

Methods: The plasma concentrations of insulin, growth hormone (GH) and ovine placental lactogen (oPL) were determined by double antibody radioimmunoassay. Insulin responsiveness to glucose was measured using bolus injection and hyperglycaemic clamp techniques in 15 non-pregnant, non-lactating ewes and in nine pregnant ewes at 105 dGA and near term at 135 dGA. Plasma samples were also collected for hormone determination. In addition to bolus injection glucose and insulin Area Under Curve calculations, the Mean Plasma Glucose Increment, Glucose Infusion Rate and Mean Plasma Insulin Increment and Area Under Curve were determined for the hyperglycaemic clamp procedures. Statistical analysis of data was conducted with Students t-tests, repeated measures ANOVA and 2-way ANOVA.

Results: Maternal growth hormone, placental lactogen and NEFA concentrations increased, while basal glucose and insulin concentrations declined with advancing gestation. At 135 dGA following bolus glucose injections, peak insulin concentrations and insulin area under curve (AUC) profiles were significantly reduced in pregnant ewes compared with NPNL control ewes (p < 0.001 and P < 0.001, respectively). In hyperglycaemic clamp studies, while maintaining glucose levels not different from NPNL ewes, pregnant ewes displayed significantly reduced insulin responses and a maintained depressed insulin secretion. In NPNL ewes, 105 and 135 dGA ewes, the Glucose Infusion Rate (GIR) was constant at approximately 5.8 mg glucose/kg/min during the last 40 minutes of the hyperglycaemic clamp and the Mean Plasma Insulin Increment (MPII) was only significantly (p < 0.001) greater in NPNL ewes. Following the clamp, NEFA concentrations were reduced by approximately 60% of pre-clamp levels in all groups, though a blunted and suppressed insulin response was maintained in 105 and 135 dGA ewes.

Conclusions: Results suggest that despite an acute suppression of circulating NEFA concentrations during pregnancy, the associated steroids and hormones of pregnancy and possibly NEFA metabolism, may act to maintain a reduced insulin output, thereby sparing glucose for non-insulin dependent placental uptake and ultimately, fetal requirements.

Citing Articles

Colostrum traits and newborn body weight and growth: comparison between single and twin underfed sheep pregnancies.

Turin J, Sales F, Peralta O, De Los Reyes M, Borie C, Carrasco A Front Vet Sci. 2023; 10:1256989.

PMID: 37745219 PMC: 10514513. DOI: 10.3389/fvets.2023.1256989.


A Randomized Crossover Intervention Study on the Effect a Standardized Maté Extract ( A. St.-Hil.) in Men Predisposed to Cardiovascular Risk.

Gebara K, Gasparotto Junior A, Palozi R, Morand C, Bonetti C, Gozzi P Nutrients. 2020; 13(1).

PMID: 33374524 PMC: 7822211. DOI: 10.3390/nu13010014.


Fluctuations of serum cortisol, insulin and non-esterified fatty acid concentrations in growing ewes over the year.

Snoj T, Jenko Z, cebulj-Kadunc N Ir Vet J. 2014; 67(1):22.

PMID: 25337389 PMC: 4203860. DOI: 10.1186/2046-0481-67-22.


Elevated maternal cortisol leads to relative maternal hyperglycemia and increased stillbirth in ovine pregnancy.

Keller-Wood M, Feng X, Wood C, Richards E, Anthony R, Dahl G Am J Physiol Regul Integr Comp Physiol. 2014; 307(4):R405-13.

PMID: 24920731 PMC: 4137155. DOI: 10.1152/ajpregu.00530.2013.


Lactogenic activity of rats stimulated by Gunnera perpensa L. (Gunneraceae) from South Africa.

Simelane M, Lawal O, Djarova T, Musabayane C, Singh M, Opoku A Afr J Tradit Complement Altern Med. 2013; 9(4):561-73.

PMID: 23983393 PMC: 3746640. DOI: 10.4314/ajtcam.v9i4.14.

References
1.
Flint D, Clegg R, Vernon R . Role of insulin receptors in the changing metabolism of adipose tissue during pregnancy and lactation in the rat. Biochem J. 1979; 182(2):421-7. PMC: 1161323. DOI: 10.1042/bj1820421. View

2.
Seufert J, Kieffer T, Leech C, Holz G, Moritz W, Ricordi C . Leptin suppression of insulin secretion and gene expression in human pancreatic islets: implications for the development of adipogenic diabetes mellitus. J Clin Endocrinol Metab. 1999; 84(2):670-6. PMC: 2927866. DOI: 10.1210/jcem.84.2.5460. View

3.
Handwerger S . Clinical counterpoint: the physiology of placental lactogen in human pregnancy. Endocr Rev. 1991; 12(4):329-36. DOI: 10.1210/edrv-12-4-329. View

4.
Regnault T, Orbus R, Battaglia F, Wilkening R, Anthony R . Altered arterial concentrations of placental hormones during maximal placental growth in a model of placental insufficiency. J Endocrinol. 1999; 162(3):433-42. DOI: 10.1677/joe.0.1620433. View

5.
Catalano P, Nizielski S, Shao J, Preston L, Qiao L, Friedman J . Downregulated IRS-1 and PPARgamma in obese women with gestational diabetes: relationship to FFA during pregnancy. Am J Physiol Endocrinol Metab. 2002; 282(3):E522-33. DOI: 10.1152/ajpendo.00124.2001. View