HOMEPRODUCTSSERVICESCOMPANYCONTACTFAQResearchDictionaryPharmaMobileSign Up FREE or Login

Innate immunity modulates adipokines in humans.

AbstractCONTEXT:
Chronic inflammation converges in type 2 diabetes and atherosclerosis. Modulation of adipokine signaling by innate immunity in humans is of considerable interest given the role of adipokines in insulin resistance and atherosclerosis.
OBJECTIVE:
The aim of the study was to examine effects of low-grade endotoxemia, a model of human inflammation, on adipokines in vivo.
DESIGN/SETTING:
An open-label, placebo-controlled, fixed-sequence clinical study was conducted at a General Clinical Research Center.
PATIENTS:
There were 20 healthy male (50%) and female volunteers aged 18-40 yr.
INTERVENTION:
Serial blood sampling and adipose biopsies were performed for 24 h before and after iv bolus endotoxin [lipopolysaccharide (LPS), 3 ng/kg].
MAIN OUTCOME MEASURES:
We measured plasma leptin, adiponectin, resistin, soluble leptin receptor, cytokines, insulin, and glucose; distribution of adiponectin among multimeric complexes; whole blood, monocyte and adipose mRNA for adipokines and their receptors.
RESULTS:
LPS induced fever, blood, and adipose TNF and IL-6 and increased homeostasis model assessment of insulin resistance. These were associated with increases in plasma leptin (from 4.1 +/- 1.1 to 6.1 +/- 1.9 ng/ml in men; 21.1 +/- 4.4 to 27.4 +/- 4.7 ng/ml in women; P < 0.005), doubling of the leptin:soluble leptin receptor ratio, and marked induction of whole blood resistin mRNA (13.7 +/- 7.3-fold; P < 0.001) and plasma resistin (8.5 +/- 2.75 to 43.2 +/- 15.3 ng/ml; P < 0.001). Although total adiponectin levels and low and high molecular weight adiponectin complexes were unaltered by LPS treatment, whole blood mRNA for adiponectin receptors 1 (49%; P < 0.005) and 2 (65%; P < 0.001) was suppressed.
CONCLUSIONS:
Modulation of adipokine signaling may contribute to the insulin resistant, atherogenic state associated with human inflammatory syndromes. Targeting of individual adipokines or their upstream regulation may prove effective in preventing acute and chronic inflammation-related metabolic complications.
AuthorsPaul D Anderson, Nehal N Mehta, Megan L Wolfe, Christine C Hinkle, Leticia Pruscino, Lynne L Comiskey, Jennifer Tabita-Martinez, Kimberly F Sellers, Michael R Rickels, Rexford S Ahima, Muredach P Reilly
JournalThe Journal of clinical endocrinology and metabolism (J Clin Endocrinol Metab) Vol. 92 Issue 6 Pg. 2272-9 (Jun 2007) ISSN: 0021-972X [Print] United States
PMID17374708 (Publication Type: Controlled Clinical Trial, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • ADIPOQ protein, human
  • Adiponectin
  • Blood Glucose
  • Cytokines
  • Insulin
  • Leptin
  • Lipopolysaccharides
  • Peptide Hormones
  • Placebos
  • RNA, Messenger
  • Receptors, Cell Surface
  • Receptors, Leptin
  • Resistin
Topics
  • Adiponectin (blood, genetics)
  • Adult
  • Blood Glucose (metabolism)
  • Cytokines (blood, genetics)
  • Endotoxemia (chemically induced, immunology, metabolism)
  • Female
  • Humans
  • Immune System (immunology, metabolism)
  • Insulin (blood)
  • Leptin (blood, genetics)
  • Lipopolysaccharides (administration & dosage)
  • Male
  • Peptide Hormones (blood, genetics)
  • Placebos
  • RNA, Messenger (metabolism)
  • Receptors, Cell Surface (blood, genetics)
  • Receptors, Leptin
  • Resistin (blood, genetics)
  • Signal Transduction (immunology)

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 network!


Choose Username:
Email:
Password:
Verify Password: