Curcumin and piperine supplementation of obese mice under caloric restriction modulates body fat and interleukin-1β

Background Dietary bioactive compounds capable of improving metabolic profiles would be of great value, especially for overweight individuals undergoing a caloric restriction (CR) regimen. Curcumin (Cur), a possible anti-obesity compound, and piperine (Pip), a plausible enhancer of Cur’s bioavailabi...

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Veröffentlicht in:Nutrition & metabolism Jg. 15; H. 1; S. 12
Hauptverfasser: Miyazawa, Taiki, Nakagawa, Kiyotaka, Kim, Sharon H., Thomas, Michael J., Paul, Ligi, Zingg, Jean-Marc, Dolnikowski, Gregory G., Roberts, Susan B., Kimura, Fumiko, Miyazawa, Teruo, Azzi, Angelo, Meydani, Mohsen
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Veröffentlicht: London BioMed Central 06.02.2018
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Abstract Background Dietary bioactive compounds capable of improving metabolic profiles would be of great value, especially for overweight individuals undergoing a caloric restriction (CR) regimen. Curcumin (Cur), a possible anti-obesity compound, and piperine (Pip), a plausible enhancer of Cur’s bioavailability and efficacy, may be candidate agents for controlling body fat, metabolism and low grade inflammation. Methods 47 eight-week-old male C57BL/6 mice were fed a high fat diet (HFD) for 23 weeks to induce obesity. Then, mice were divided into 5 groups. Group 1 continued on HFD ad libitum. The other 4 groups underwent CR (reduced 10% HFD intake for 10 weeks, 20% for 20 weeks) with Cur, Pip, Cur + Pip or none of these. Percent body fat, plasma inflammatory markers associated with obesity (interferon (IFN)-γ, interleukin (IL)-10, IL-12 p70, IL-1β, IL-6 and KC/GRO), plasma Cur metabolites and liver telomere length were measured. Results Compared to the other groups, obese mice who underwent CR and received Cur + Pip in their diet lost more fat and had significantly lower IL-1β and KC/GRO. Tandem mass spectrometry analysis of plasma from obese mice under CR showed no difference in Cur metabolite levels between groups supplemented with Cur alone or combined with Pip. However, plasma IL-1β levels were inversely correlated with curcumin glucuronide. Minor modulation of telomere length were observed. Conclusions It is plausible that supplementing the high fat diet of CR mice with Cur + Pip may increase loss of body fat and suppresses HFD induced inflammation. Combination of Cur and Pip has potential to enhance CR effects for the prevention of metabolic syndrome.
AbstractList Background Dietary bioactive compounds capable of improving metabolic profiles would be of great value, especially for overweight individuals undergoing a caloric restriction (CR) regimen. Curcumin (Cur), a possible anti-obesity compound, and piperine (Pip), a plausible enhancer of Cur’s bioavailability and efficacy, may be candidate agents for controlling body fat, metabolism and low grade inflammation. Methods 47 eight-week-old male C57BL/6 mice were fed a high fat diet (HFD) for 23 weeks to induce obesity. Then, mice were divided into 5 groups. Group 1 continued on HFD ad libitum. The other 4 groups underwent CR (reduced 10% HFD intake for 10 weeks, 20% for 20 weeks) with Cur, Pip, Cur + Pip or none of these. Percent body fat, plasma inflammatory markers associated with obesity (interferon (IFN)-γ, interleukin (IL)-10, IL-12 p70, IL-1β, IL-6 and KC/GRO), plasma Cur metabolites and liver telomere length were measured. Results Compared to the other groups, obese mice who underwent CR and received Cur + Pip in their diet lost more fat and had significantly lower IL-1β and KC/GRO. Tandem mass spectrometry analysis of plasma from obese mice under CR showed no difference in Cur metabolite levels between groups supplemented with Cur alone or combined with Pip. However, plasma IL-1β levels were inversely correlated with curcumin glucuronide. Minor modulation of telomere length were observed. Conclusions It is plausible that supplementing the high fat diet of CR mice with Cur + Pip may increase loss of body fat and suppresses HFD induced inflammation. Combination of Cur and Pip has potential to enhance CR effects for the prevention of metabolic syndrome.
BACKGROUND: Dietary bioactive compounds capable of improving metabolic profiles would be of great value, especially for overweight individuals undergoing a caloric restriction (CR) regimen. Curcumin (Cur), a possible anti-obesity compound, and piperine (Pip), a plausible enhancer of Cur’s bioavailability and efficacy, may be candidate agents for controlling body fat, metabolism and low grade inflammation. METHODS: 47 eight-week-old male C57BL/6 mice were fed a high fat diet (HFD) for 23 weeks to induce obesity. Then, mice were divided into 5 groups. Group 1 continued on HFD ad libitum. The other 4 groups underwent CR (reduced 10% HFD intake for 10 weeks, 20% for 20 weeks) with Cur, Pip, Cur + Pip or none of these. Percent body fat, plasma inflammatory markers associated with obesity (interferon (IFN)-γ, interleukin (IL)-10, IL-12 p70, IL-1β, IL-6 and KC/GRO), plasma Cur metabolites and liver telomere length were measured. RESULTS: Compared to the other groups, obese mice who underwent CR and received Cur + Pip in their diet lost more fat and had significantly lower IL-1β and KC/GRO. Tandem mass spectrometry analysis of plasma from obese mice under CR showed no difference in Cur metabolite levels between groups supplemented with Cur alone or combined with Pip. However, plasma IL-1β levels were inversely correlated with curcumin glucuronide. Minor modulation of telomere length were observed. CONCLUSIONS: It is plausible that supplementing the high fat diet of CR mice with Cur + Pip may increase loss of body fat and suppresses HFD induced inflammation. Combination of Cur and Pip has potential to enhance CR effects for the prevention of metabolic syndrome.
Dietary bioactive compounds capable of improving metabolic profiles would be of great value, especially for overweight individuals undergoing a caloric restriction (CR) regimen. Curcumin (Cur), a possible anti-obesity compound, and piperine (Pip), a plausible enhancer of Cur's bioavailability and efficacy, may be candidate agents for controlling body fat, metabolism and low grade inflammation.BACKGROUNDDietary bioactive compounds capable of improving metabolic profiles would be of great value, especially for overweight individuals undergoing a caloric restriction (CR) regimen. Curcumin (Cur), a possible anti-obesity compound, and piperine (Pip), a plausible enhancer of Cur's bioavailability and efficacy, may be candidate agents for controlling body fat, metabolism and low grade inflammation.47 eight-week-old male C57BL/6 mice were fed a high fat diet (HFD) for 23 weeks to induce obesity. Then, mice were divided into 5 groups. Group 1 continued on HFD ad libitum. The other 4 groups underwent CR (reduced 10% HFD intake for 10 weeks, 20% for 20 weeks) with Cur, Pip, Cur + Pip or none of these. Percent body fat, plasma inflammatory markers associated with obesity (interferon (IFN)-γ, interleukin (IL)-10, IL-12 p70, IL-1β, IL-6 and KC/GRO), plasma Cur metabolites and liver telomere length were measured.METHODS47 eight-week-old male C57BL/6 mice were fed a high fat diet (HFD) for 23 weeks to induce obesity. Then, mice were divided into 5 groups. Group 1 continued on HFD ad libitum. The other 4 groups underwent CR (reduced 10% HFD intake for 10 weeks, 20% for 20 weeks) with Cur, Pip, Cur + Pip or none of these. Percent body fat, plasma inflammatory markers associated with obesity (interferon (IFN)-γ, interleukin (IL)-10, IL-12 p70, IL-1β, IL-6 and KC/GRO), plasma Cur metabolites and liver telomere length were measured.Compared to the other groups, obese mice who underwent CR and received Cur + Pip in their diet lost more fat and had significantly lower IL-1β and KC/GRO. Tandem mass spectrometry analysis of plasma from obese mice under CR showed no difference in Cur metabolite levels between groups supplemented with Cur alone or combined with Pip. However, plasma IL-1β levels were inversely correlated with curcumin glucuronide. Minor modulation of telomere length were observed.RESULTSCompared to the other groups, obese mice who underwent CR and received Cur + Pip in their diet lost more fat and had significantly lower IL-1β and KC/GRO. Tandem mass spectrometry analysis of plasma from obese mice under CR showed no difference in Cur metabolite levels between groups supplemented with Cur alone or combined with Pip. However, plasma IL-1β levels were inversely correlated with curcumin glucuronide. Minor modulation of telomere length were observed.It is plausible that supplementing the high fat diet of CR mice with Cur + Pip may increase loss of body fat and suppresses HFD induced inflammation. Combination of Cur and Pip has potential to enhance CR effects for the prevention of metabolic syndrome.CONCLUSIONSIt is plausible that supplementing the high fat diet of CR mice with Cur + Pip may increase loss of body fat and suppresses HFD induced inflammation. Combination of Cur and Pip has potential to enhance CR effects for the prevention of metabolic syndrome.
Dietary bioactive compounds capable of improving metabolic profiles would be of great value, especially for overweight individuals undergoing a caloric restriction (CR) regimen. Curcumin (Cur), a possible anti-obesity compound, and piperine (Pip), a plausible enhancer of Cur's bioavailability and efficacy, may be candidate agents for controlling body fat, metabolism and low grade inflammation. 47 eight-week-old male C57BL/6 mice were fed a high fat diet (HFD) for 23 weeks to induce obesity. Then, mice were divided into 5 groups. Group 1 continued on HFD ad libitum. The other 4 groups underwent CR (reduced 10% HFD intake for 10 weeks, 20% for 20 weeks) with Cur, Pip, Cur + Pip or none of these. Percent body fat, plasma inflammatory markers associated with obesity (interferon (IFN)-γ, interleukin (IL)-10, IL-12 p70, IL-1β, IL-6 and KC/GRO), plasma Cur metabolites and liver telomere length were measured. Compared to the other groups, obese mice who underwent CR and received Cur + Pip in their diet lost more fat and had significantly lower IL-1β and KC/GRO. Tandem mass spectrometry analysis of plasma from obese mice under CR showed no difference in Cur metabolite levels between groups supplemented with Cur alone or combined with Pip. However, plasma IL-1β levels were inversely correlated with curcumin glucuronide. Minor modulation of telomere length were observed. It is plausible that supplementing the high fat diet of CR mice with Cur + Pip may increase loss of body fat and suppresses HFD induced inflammation. Combination of Cur and Pip has potential to enhance CR effects for the prevention of metabolic syndrome.
Abstract Background Dietary bioactive compounds capable of improving metabolic profiles would be of great value, especially for overweight individuals undergoing a caloric restriction (CR) regimen. Curcumin (Cur), a possible anti-obesity compound, and piperine (Pip), a plausible enhancer of Cur’s bioavailability and efficacy, may be candidate agents for controlling body fat, metabolism and low grade inflammation. Methods 47 eight-week-old male C57BL/6 mice were fed a high fat diet (HFD) for 23 weeks to induce obesity. Then, mice were divided into 5 groups. Group 1 continued on HFD ad libitum. The other 4 groups underwent CR (reduced 10% HFD intake for 10 weeks, 20% for 20 weeks) with Cur, Pip, Cur + Pip or none of these. Percent body fat, plasma inflammatory markers associated with obesity (interferon (IFN)-γ, interleukin (IL)-10, IL-12 p70, IL-1β, IL-6 and KC/GRO), plasma Cur metabolites and liver telomere length were measured. Results Compared to the other groups, obese mice who underwent CR and received Cur + Pip in their diet lost more fat and had significantly lower IL-1β and KC/GRO. Tandem mass spectrometry analysis of plasma from obese mice under CR showed no difference in Cur metabolite levels between groups supplemented with Cur alone or combined with Pip. However, plasma IL-1β levels were inversely correlated with curcumin glucuronide. Minor modulation of telomere length were observed. Conclusions It is plausible that supplementing the high fat diet of CR mice with Cur + Pip may increase loss of body fat and suppresses HFD induced inflammation. Combination of Cur and Pip has potential to enhance CR effects for the prevention of metabolic syndrome.
ArticleNumber 12
Audience Academic
Author Miyazawa, Taiki
Nakagawa, Kiyotaka
Miyazawa, Teruo
Paul, Ligi
Azzi, Angelo
Meydani, Mohsen
Zingg, Jean-Marc
Roberts, Susan B.
Kim, Sharon H.
Kimura, Fumiko
Thomas, Michael J.
Dolnikowski, Gregory G.
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  surname: Miyazawa
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  organization: Vascular Biology Laboratory, Jean Mayer USDA-Human Nutrition Research Center on Aging, (HNRCA) at Tufts University, Food and Biodynamic Chemistry Laboratory, Graduate School of Agricultural Science, Tohoku University
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  givenname: Kiyotaka
  orcidid: 0000-0003-3026-7358
  surname: Nakagawa
  fullname: Nakagawa, Kiyotaka
  email: nkgw@m.tohoku.ac.jp
  organization: Vascular Biology Laboratory, Jean Mayer USDA-Human Nutrition Research Center on Aging, (HNRCA) at Tufts University, Food and Biodynamic Chemistry Laboratory, Graduate School of Agricultural Science, Tohoku University
– sequence: 3
  givenname: Sharon H.
  surname: Kim
  fullname: Kim, Sharon H.
  organization: Vascular Biology Laboratory, Jean Mayer USDA-Human Nutrition Research Center on Aging, (HNRCA) at Tufts University
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  givenname: Michael J.
  surname: Thomas
  fullname: Thomas, Michael J.
  organization: Vascular Biology Laboratory, Jean Mayer USDA-Human Nutrition Research Center on Aging, (HNRCA) at Tufts University
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  givenname: Ligi
  surname: Paul
  fullname: Paul, Ligi
  organization: Vitamin Metabolism Laboratory, Jean Mayer USDA-Human Nutrition Research Center on Aging, (HNRCA) at Tufts University
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  givenname: Jean-Marc
  surname: Zingg
  fullname: Zingg, Jean-Marc
  organization: Department of Biochemistry and Molecular Biology, Miller School of Medicine, University of Miami
– sequence: 7
  givenname: Gregory G.
  surname: Dolnikowski
  fullname: Dolnikowski, Gregory G.
  organization: Mass Spectrometry Laboratory, Jean Mayer USDA-Human Nutrition Research Center on Aging, (HNRCA) at Tufts University
– sequence: 8
  givenname: Susan B.
  surname: Roberts
  fullname: Roberts, Susan B.
  organization: Energy Metabolism Laboratory, Jean Mayer USDA-Human Nutrition Research Center on Aging, (HNRCA) at Tufts University
– sequence: 9
  givenname: Fumiko
  surname: Kimura
  fullname: Kimura, Fumiko
  organization: Food and Biodynamic Chemistry Laboratory, Graduate School of Agricultural Science, Tohoku University
– sequence: 10
  givenname: Teruo
  surname: Miyazawa
  fullname: Miyazawa, Teruo
  organization: Food and Biotechnology Innovation Project, New Industry Creation Hatchery Center (NICHe), Tohoku University, Food and Health Science Research Unit, Graduate School of Agricultural Science, Tohoku University
– sequence: 11
  givenname: Angelo
  surname: Azzi
  fullname: Azzi, Angelo
  organization: Vascular Biology Laboratory, Jean Mayer USDA-Human Nutrition Research Center on Aging, (HNRCA) at Tufts University
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  givenname: Mohsen
  surname: Meydani
  fullname: Meydani, Mohsen
  organization: Vascular Biology Laboratory, Jean Mayer USDA-Human Nutrition Research Center on Aging, (HNRCA) at Tufts University
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Issue 1
Keywords Obesity
Tandem mass spectrometry
Meso scale discovery
Piperine
Curcumin
Inflammation
Metabolic syndrome
Glucuronide
Caloric restriction
High fat diet
Language English
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Snippet Background Dietary bioactive compounds capable of improving metabolic profiles would be of great value, especially for overweight individuals undergoing a...
Dietary bioactive compounds capable of improving metabolic profiles would be of great value, especially for overweight individuals undergoing a caloric...
BACKGROUND: Dietary bioactive compounds capable of improving metabolic profiles would be of great value, especially for overweight individuals undergoing a...
Abstract Background Dietary bioactive compounds capable of improving metabolic profiles would be of great value, especially for overweight individuals...
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SubjectTerms Adipose tissues
Alkaloids
animal disease models
bioactive compounds
bioavailability
Caloric restriction
Care and treatment
Clinical Nutrition
Control
Curcumin
Glucuronide
Health aspects
High fat diet
Inflammation
interferon-gamma
Interleukin-1
interleukin-12
interleukin-1beta
interleukin-6
liver
Low-calorie diet
males
Medicine
Medicine & Public Health
Meso scale discovery
Metabolic Diseases
metabolic syndrome
metabolism
metabolites
mice
Obesity
tandem mass spectrometry
telomeres
Turmeric
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Title Curcumin and piperine supplementation of obese mice under caloric restriction modulates body fat and interleukin-1β
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