25 ADIPOSITY AND PRO-ATHEROSCLEROTIC RESPONSES TO INNATE IMMUNE CHALLENGE IN HUMANS. (1st March 2005)
- Record Type:
- Journal Article
- Title:
- 25 ADIPOSITY AND PRO-ATHEROSCLEROTIC RESPONSES TO INNATE IMMUNE CHALLENGE IN HUMANS. (1st March 2005)
- Main Title:
- 25 ADIPOSITY AND PRO-ATHEROSCLEROTIC RESPONSES TO INNATE IMMUNE CHALLENGE IN HUMANS
- Authors:
- Mehta, N. N.
Anderson, P. D.
Wolfe, M.
Rickels, M.
Zemel, B.
Hinkle, C.
Comiskey, L.
Tabita-Martinez, J.
Ahima, R.
Rader, D. J.
Reilly, M. P. - Abstract:
- Abstract : Purpose: A convergence of inflammatory and adipose signals has been proposed as a mechanism for metabolic syndrome and atherosclerosis. We hypothesized that adipose tissue may influence the response to acute inflammation in vivo in humans. Method: As part of a sixty-hour GCRC protocol of 20 healthy volunteers [50% male, 80% Caucasian, mean age 27.3 ± 4.8; 10 lean (BMI = 20.55 ± 1.75) and 10 overweight (BMI = 27.08 ± 0.88)], we examined peak responses in serial whole blood and adipose (subcutaneous fat biopsies) gene expression, and plasma hs-C reactive protein (hs-CRP) following intravenous administration of 3 ng/kg human research grade endotoxin. Findings: As expected, we observed increases (median fold increase and inter-quartile range) in whole blood mRNA expression of TNF alpha [8.8 fold (6.2-12.0)], IL-6 [3.8 (1.7-7.5)] and IL-10 [5.1 (2.4-7.7)], as well as plasma hs-CRP levels (mean peak hs-CRP 44.5 ± 21.7) following intravenous endotoxin (p<0.01 for all). Remarkably, there were marked increases in adipose mRNA levels of IL-6 [76.4 fold (45.4-154.3), p<0.001] as well as increases in TNF-alpha [5.3 (1.8-7.7), p<0.01], leptin [1.7 (1.4-2.2), p<0.05] and PPAR-alpha [2.8 (1.9-4.1), p<0.05]. Although not statistically significant in this small sample, peak plasma CRP levels (50.3 ± 27.0 versus 38.8 [138} 13.8, p = 0.1) tended to be higher and fold increase in whole blood IL-10 mRNA levels (3.74 versus 5.98, p = 0.3), an anti-inflammatory anti-atheroscleroticAbstract : Purpose: A convergence of inflammatory and adipose signals has been proposed as a mechanism for metabolic syndrome and atherosclerosis. We hypothesized that adipose tissue may influence the response to acute inflammation in vivo in humans. Method: As part of a sixty-hour GCRC protocol of 20 healthy volunteers [50% male, 80% Caucasian, mean age 27.3 ± 4.8; 10 lean (BMI = 20.55 ± 1.75) and 10 overweight (BMI = 27.08 ± 0.88)], we examined peak responses in serial whole blood and adipose (subcutaneous fat biopsies) gene expression, and plasma hs-C reactive protein (hs-CRP) following intravenous administration of 3 ng/kg human research grade endotoxin. Findings: As expected, we observed increases (median fold increase and inter-quartile range) in whole blood mRNA expression of TNF alpha [8.8 fold (6.2-12.0)], IL-6 [3.8 (1.7-7.5)] and IL-10 [5.1 (2.4-7.7)], as well as plasma hs-CRP levels (mean peak hs-CRP 44.5 ± 21.7) following intravenous endotoxin (p<0.01 for all). Remarkably, there were marked increases in adipose mRNA levels of IL-6 [76.4 fold (45.4-154.3), p<0.001] as well as increases in TNF-alpha [5.3 (1.8-7.7), p<0.01], leptin [1.7 (1.4-2.2), p<0.05] and PPAR-alpha [2.8 (1.9-4.1), p<0.05]. Although not statistically significant in this small sample, peak plasma CRP levels (50.3 ± 27.0 versus 38.8 [138} 13.8, p = 0.1) tended to be higher and fold increase in whole blood IL-10 mRNA levels (3.74 versus 5.98, p = 0.3), an anti-inflammatory anti-atherosclerotic cytokine, tended to be lower in overweight subjects compared to lean. Conclusions: Our findings demonstrate, for the first time, that human adipose gene expression is regulated by activation of innate immunity in vivo, and preliminary analyses suggest that the response to an inflammatory stimulus may be influenced by the degree of adiposity. These observations provide novel insight into the role of adipose in promoting pro-atherosclerotic inflammatory responses in humans. … (more)
- Is Part Of:
- Journal of investigative medicine. Volume 53:Number 2(2005)
- Journal:
- Journal of investigative medicine
- Issue:
- Volume 53:Number 2(2005)
- Issue Display:
- Volume 53, Issue 2 (2005)
- Year:
- 2005
- Volume:
- 53
- Issue:
- 2
- Issue Sort Value:
- 2005-0053-0002-0000
- Page Start:
- S391
- Page End:
- S391
- Publication Date:
- 2005-03-01
- Subjects:
- Clinical medicine -- Periodicals
Medicine -- Research -- Periodicals
Medicine
Research -- United States
Clinical medicine
Medicine -- Research
Periodicals
616.075 - Journal URLs:
- http://journals.lww.com/jinvestigativemed/pages/default.aspx ↗
http://jim.bmj.com/ ↗
https://journals.sagepub.com/home/IMJ ↗
http://journals.lww.com ↗ - DOI:
- 10.2310/6650.2005.00205.24 ↗
- Languages:
- English
- ISSNs:
- 1081-5589
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5008.010000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 17966.xml