Palmitoyl-carnitine production by blood cells associates with the concentration of circulating acyl-carnitines in healthy overweight women. Issue 5 (October 2017)
- Record Type:
- Journal Article
- Title:
- Palmitoyl-carnitine production by blood cells associates with the concentration of circulating acyl-carnitines in healthy overweight women. Issue 5 (October 2017)
- Main Title:
- Palmitoyl-carnitine production by blood cells associates with the concentration of circulating acyl-carnitines in healthy overweight women
- Authors:
- Chondronikola, Maria
Asghar, Rabia
Zhang, Xiaojun
Dillon, Edgar L.
Durham, William J.
Wu, Zhanpin
Porter, Craig
Camacho-Hughes, Maria
Zhao, Yingxin
Brasier, Allan R.
Volpi, Elena
Sheffield-Moore, Melinda
Abate, Nicola
Sidossis, Labros
Tuvdendorj, Demidmaa - Abstract:
- Summary: Background: Circulating acyl-carnitines (acyl-CNTs) are associated with insulin resistance (IR) and type 2 diabetes (T2D) in both rodents and humans. However, the mechanisms whereby circulating acyl-CNTs are increased in these conditions and their role in whole-body metabolism remains unknown. The purpose of this study was to determine if, in humans, blood cells contribute in production of circulating acyl-CNTs and associate with whole-body fat metabolism. Methods and results: Eight non-diabetic healthy women (age: 47 ± 19 y; BMI: 26 ± 1 kg·m −2 ) underwent stable isotope tracer infusion and hyperinsulinemic-euglycemic clamp study to determine in vivo whole-body fatty acid flux and insulin sensitivity. Blood samples collected at baseline (0 min) and after 3 h of clamp were used to determine the synthesis rate of palmitoyl-carnitine (palmitoyl-CNT) in vitro . The fractional synthesis rate of palmitoyl-CNT was significantly higher during hyperinsulinemia (0.788 ± 0.084 vs . 0.318 ± 0.012%·hr −1, p = 0.001); however, the absolute synthesis rate (ASR) did not differ between the periods ( p = 0.809) due to ∼30% decrease in blood palmitoyl-CNT concentration ( p = 0.189) during hyperinsulinemia. The ASR of palmitoyl-CNT significantly correlated with the concentration of acyl-CNTs in basal ( r = 0.992, p < 0.001) and insulin ( r = 0.919, p = 0.001) periods; and the basal ASR significantly correlated with plasma palmitate oxidation ( r = 0.764, p = 0.027).Summary: Background: Circulating acyl-carnitines (acyl-CNTs) are associated with insulin resistance (IR) and type 2 diabetes (T2D) in both rodents and humans. However, the mechanisms whereby circulating acyl-CNTs are increased in these conditions and their role in whole-body metabolism remains unknown. The purpose of this study was to determine if, in humans, blood cells contribute in production of circulating acyl-CNTs and associate with whole-body fat metabolism. Methods and results: Eight non-diabetic healthy women (age: 47 ± 19 y; BMI: 26 ± 1 kg·m −2 ) underwent stable isotope tracer infusion and hyperinsulinemic-euglycemic clamp study to determine in vivo whole-body fatty acid flux and insulin sensitivity. Blood samples collected at baseline (0 min) and after 3 h of clamp were used to determine the synthesis rate of palmitoyl-carnitine (palmitoyl-CNT) in vitro . The fractional synthesis rate of palmitoyl-CNT was significantly higher during hyperinsulinemia (0.788 ± 0.084 vs . 0.318 ± 0.012%·hr −1, p = 0.001); however, the absolute synthesis rate (ASR) did not differ between the periods ( p = 0.809) due to ∼30% decrease in blood palmitoyl-CNT concentration ( p = 0.189) during hyperinsulinemia. The ASR of palmitoyl-CNT significantly correlated with the concentration of acyl-CNTs in basal ( r = 0.992, p < 0.001) and insulin ( r = 0.919, p = 0.001) periods; and the basal ASR significantly correlated with plasma palmitate oxidation ( r = 0.764, p = 0.027). Conclusion: In women, blood cells contribute to plasma acyl-CNT levels and the acyl-CNT production is linked to plasma palmitate oxidation, a marker of whole-body fat metabolism. Future studies are needed to confirm the role of blood cells in acyl-CNT and lipid metabolism under different physiological (i.e., in response to meal) and pathological (i.e., hyperlipidemia, IR and T2D) conditions. … (more)
- Is Part Of:
- Clinical nutrition. Volume 36:Issue 5(2017:Oct.)
- Journal:
- Clinical nutrition
- Issue:
- Volume 36:Issue 5(2017:Oct.)
- Issue Display:
- Volume 36, Issue 5 (2017)
- Year:
- 2017
- Volume:
- 36
- Issue:
- 5
- Issue Sort Value:
- 2017-0036-0005-0000
- Page Start:
- 1310
- Page End:
- 1319
- Publication Date:
- 2017-10
- Subjects:
- Acyl-carnitines -- Blood cells -- Stable isotope tracer -- Plasma palmitate oxidation -- Insulin resistance
Critically ill -- Nutrition -- Periodicals
Diet therapy -- Periodicals
Parenteral feeding -- Periodicals
Enteral feeding -- Periodicals
Enteral Nutrition -- Periodicals
Parenteral Nutrition -- Periodicals
Metabolism -- Periodicals
Diétothérapie -- Périodiques
Alimentation parentérale -- Périodiques
Alimentation entérale -- Périodiques
Nutrition -- Périodiques
Diet therapy
Enteral feeding
Nutrition
Parenteral feeding
Electronic journals
Periodicals
Electronic journals
615.854 - Journal URLs:
- http://www.sciencedirect.com/science/journal/02615614 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.clnu.2016.08.019 ↗
- Languages:
- English
- ISSNs:
- 0261-5614
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- Legaldeposit
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