HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Prenatal exposure to lipopolysaccharide combined with pre- and postnatal high-fat diet result in lowered blood pressure and insulin resistance in offspring rats.

AbstractBACKGROUND:
Adult metabolic syndrome may in part have origins in fetal or early life. This study was designed to explore the effect of prenatal exposure to lipopolysaccharide and high-fat diet on metabolic syndrome in offspring rats.
METHODS:
32 pregnant rats were randomly divided into four groups, including Control group; LPS group (pregnant rats were injected with LPS 0.4 mg/kg intraperitoneally on the 8(th), 10(th) and 12(th) day of pregnancy); High-fat group (maternal rats had high-fat diet during pregnancy and lactation period, and their pups also had high-fat diet up to the third month of life); LPS + High-fat group (rats were exposed to the identical experimental scheme with LPS group and High-fat group).
RESULTS:
Blood pressure elevated in LPS group and High-fat group, reduced in LPS+High-fat group, accompanied by the increase of serum leptin level in LPS and High-fat group and increase of serum IL-6, TNF-a in High-fat group; both serum insulin and cholesterol increased in High-fat and LPS+High-fat group, as well as insulin in LPS group. HOMA-IR value increased in LPS, High-fat and LPS+High-fat group, and QUICKI decreased in these groups; H-E staining showed morphologically pathological changes in thoracic aorta and liver tissue in the three groups. Increased serum alanine and aspartate aminotransferase suggest impaired liver function in LPS+High-fat group.
CONCLUSION/SIGNIFICANCE:
Prenatal exposure to lipopolysaccharide combined with pre- and postnatal high-fat diet result in lowered blood pressure, insulin resistance and impaired liver function in three-month old offspring rats. The lowered blood pressure might benefit from the predictive adaptive response to prenatal inflammation.
AuthorsXue-Qin Hao, Jing-Xia Du, Yan Li, Meng Li, Shou-Yan Zhang
JournalPloS one (PLoS One) Vol. 9 Issue 2 Pg. e88127 ( 2014) ISSN: 1932-6203 [Electronic] United States
PMID24498431 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Blood Glucose
  • Cytokines
  • Insulin
  • Lipopolysaccharides
  • Triglycerides
  • Cholesterol
Topics
  • Animals
  • Animals, Newborn
  • Blood Glucose (metabolism)
  • Blood Pressure (drug effects)
  • Body Weight
  • Cholesterol (metabolism)
  • Cytokines (metabolism)
  • Diet, High-Fat (adverse effects)
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Insulin (metabolism)
  • Insulin Resistance
  • Kidney Function Tests
  • Lipopolysaccharides (adverse effects)
  • Liver Function Tests
  • Male
  • Metabolic Syndrome (etiology, metabolism, pathology)
  • Pregnancy
  • Prenatal Exposure Delayed Effects (etiology)
  • Rats
  • Rats, Sprague-Dawley
  • Triglycerides (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: