Document Detail


Pre-weaning growth hormone treatment reverses hypertension and endothelial dysfunction in adult male offspring of mothers undernourished during pregnancy.
MedLine Citation:
PMID:  23308239     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Maternal undernutrition results in elevated blood pressure (BP) and endothelial dysfunction in adult offspring. However, few studies have investigated interventions during early life to ameliorate the programming of hypertension and vascular disorders. We have utilised a model of maternal undernutrition to examine the effects of pre-weaning growth hormone (GH) treatment on BP and vascular function in adulthood. Female Sprague-Dawley rats were fed either a standard control diet (CON) or 50% of CON intake throughout pregnancy (UN). From neonatal day 3 until weaning (day 21), CON and UN pups received either saline (CON-S, UN-S) or GH (2.5 ug/g/day)(CON-GH, UN-GH). All dams were fed ad libitum throughout lactation. Male offspring were fed a standard diet until the end of the study. Systolic blood pressure (SBP) was measured at day 150 by tail cuff plethysmography. At day 160, intact mesenteric vessels mounted on a pressure myograph. Responses to pressure, agonist-induced constriction and endothelium-dependent vasodilators were investigated to determine vascular function. SBP was increased in UN-S groups and normalised in UN-GH groups (CON-S 121±2 mmHg, CON-GH 115±3, UN-S 146±3, UN-GH 127±2). Pressure mediated dilation was reduced in UN-S offspring and normalised in UN-GH groups. Vessels from UN-S offspring demonstrated a reduced constrictor response to phenylephrine and reduced vasodilator response to acetylcholine (ACh). Furthermore, UN-S offspring vessels displayed a reduced vasodilator response in the presence of L-NG-Nitroarginine Methyl Ester (L-NAME), carbenoxolone (CBX), L-NAME and CBX, Tram-34 and Apamin. UN-GH vessels showed little difference in responses when compared to CON and significantly increased vasodilator responses when compared to UN-S offspring. Pre-weaning GH treatment reverses the negative effects of maternal UN on SBP and vasomotor function in adult offspring. These data suggest that developmental cardiovascular programming is potentially reversible by early life GH treatment and that GH can reverse the vascular adaptations resulting from maternal undernutrition.
Authors:
Clint Gray; Minglan Li; Clare M Reynolds; Mark H Vickers
Related Documents :
12203919 - A new intracoronary measurement catheter, metricath, compared to intravascular ultrasou...
24670329 - Redox mechanisms of the beneficial effects of heme oxygenase in hypertension.
1643469 - Use of teflon stents for lymphovenous anastomosis.
3708639 - Haemodynamic consequences of arterial replacement with a synthetic graft.
15472599 - Direct intra-aneurysm sac pressure measurement using tip-pressure sensors: in vivo and ...
3229019 - Intravenous labetalol for the control of hypertension following repair of coarctation o...
21724009 - Anaesthesia for caesarean section in a patient with lumbar syringomyelia.
15050099 - The dynamic placenta: ii. hypothetical model of a fetus driven transplacental water bal...
17714539 - Brain haemodynamic effects of nasal continuous airway pressure in preterm infants of le...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2013-01-07
Journal Detail:
Title:  PloS one     Volume:  8     ISSN:  1932-6203     ISO Abbreviation:  PLoS ONE     Publication Date:  2013  
Date Detail:
Created Date:  2013-01-11     Completed Date:  2013-07-02     Revised Date:  2013-07-11    
Medline Journal Info:
Nlm Unique ID:  101285081     Medline TA:  PLoS One     Country:  United States    
Other Details:
Languages:  eng     Pagination:  e53505     Citation Subset:  IM    
Affiliation:
Liggins Institute and Gravida, National Centre for Growth and Development, University of Auckland, Auckland, New Zealand. c.gray@auckland.ac.nz
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Acetylcholine / pharmacology
Adult
Animals
Apamin / pharmacology
Blood Pressure / drug effects*
Carbenoxolone / pharmacology
Female
Growth Hormone / pharmacology*
Humans
Hypertension / physiopathology,  prevention & control*
Male
Malnutrition / physiopathology
Mesenteric Arteries / drug effects*
NG-Nitroarginine Methyl Ester / pharmacology
Phenylephrine / pharmacology
Pregnancy
Pyrazoles / pharmacology
Rats
Rats, Sprague-Dawley
Time Factors
Vasoconstriction / drug effects*
Vasodilation / drug effects*
Weaning
Chemical
Reg. No./Substance:
0/Pyrazoles; 0/TRAM 34; 24345-16-2/Apamin; 50903-99-6/NG-Nitroarginine Methyl Ester; 51-84-3/Acetylcholine; 5697-56-3/Carbenoxolone; 59-42-7/Phenylephrine; 9002-72-6/Growth Hormone
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Use of PB-Cre4 mice for mosaic gene deletion.
Next Document:  High-resolution micro-CT for morphologic and quantitative assessment of the sinusoid in human cavern...