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Efficacy of tomato concentrates in mouse models of dyslipidemia and cancer

We previously reported that adding freeze-dried tomato powder from transgenic plants expressing the apolipoprotein A-I mimetic peptide 6F at 2.2% by weight to a Western diet (WD) ameliorated dyslipidemia and atherosclerosis in mice. The same dose in a human would require three cups of tomato powder...

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Autores principales: Chattopadhyay, Arnab, Grijalva, Victor, Hough, Greg, Su, Feng, Mukherjee, Pallavi, Farias-Eisner, Robin, Anantharamaiah, G M, Faull, Kym F, Hwang, Lin H, Navab, Mohamad, Fogelman, Alan M, Reddy, Srinivasa T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4492730/
https://www.ncbi.nlm.nih.gov/pubmed/26171234
http://dx.doi.org/10.1002/prp2.154
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author Chattopadhyay, Arnab
Grijalva, Victor
Hough, Greg
Su, Feng
Mukherjee, Pallavi
Farias-Eisner, Robin
Anantharamaiah, G M
Faull, Kym F
Hwang, Lin H
Navab, Mohamad
Fogelman, Alan M
Reddy, Srinivasa T
author_facet Chattopadhyay, Arnab
Grijalva, Victor
Hough, Greg
Su, Feng
Mukherjee, Pallavi
Farias-Eisner, Robin
Anantharamaiah, G M
Faull, Kym F
Hwang, Lin H
Navab, Mohamad
Fogelman, Alan M
Reddy, Srinivasa T
author_sort Chattopadhyay, Arnab
collection PubMed
description We previously reported that adding freeze-dried tomato powder from transgenic plants expressing the apolipoprotein A-I mimetic peptide 6F at 2.2% by weight to a Western diet (WD) ameliorated dyslipidemia and atherosclerosis in mice. The same dose in a human would require three cups of tomato powder three times daily. To reduce the volume, we sought a method to concentrate 6F. Remarkably, extracting the transgenic freeze-dried tomato overnight in ethyl acetate with 5% acetic acid resulted in a 37-fold reduction in the amount of transgenic tomato needed for biologic activity. In a mouse model of dyslipidemia, adding 0.06% by weight of the tomato concentrate expressing the 6F peptide (Tg6F) to a WD significantly reduced plasma total cholesterol and triglycerides (P < 0.0065). In a mouse model of colon cancer metastatic to the lungs, adding 0.06% of Tg6F, but not a control tomato concentrate (EV), to standard mouse chow reduced tumor-associated neutrophils by 94 ± 1.1% (P = 0.0052), and reduced tumor burden by two-thirds (P = 0.0371). Adding 0.06% of either EV or Tg6F by weight to standard mouse chow significantly reduced tumor burden in a mouse model of ovarian cancer; however, Tg6F was significantly more effective (35% reduction for EV vs. 53% reduction for Tg6F; P = 0.0069). Providing the same dose of tomato concentrate to humans would require only two tablespoons three times daily making this a practical approach for testing oral apoA-I mimetic therapy in the treatment of dyslipidemia and cancer.
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spelling pubmed-44927302015-07-13 Efficacy of tomato concentrates in mouse models of dyslipidemia and cancer Chattopadhyay, Arnab Grijalva, Victor Hough, Greg Su, Feng Mukherjee, Pallavi Farias-Eisner, Robin Anantharamaiah, G M Faull, Kym F Hwang, Lin H Navab, Mohamad Fogelman, Alan M Reddy, Srinivasa T Pharmacol Res Perspect Original Articles We previously reported that adding freeze-dried tomato powder from transgenic plants expressing the apolipoprotein A-I mimetic peptide 6F at 2.2% by weight to a Western diet (WD) ameliorated dyslipidemia and atherosclerosis in mice. The same dose in a human would require three cups of tomato powder three times daily. To reduce the volume, we sought a method to concentrate 6F. Remarkably, extracting the transgenic freeze-dried tomato overnight in ethyl acetate with 5% acetic acid resulted in a 37-fold reduction in the amount of transgenic tomato needed for biologic activity. In a mouse model of dyslipidemia, adding 0.06% by weight of the tomato concentrate expressing the 6F peptide (Tg6F) to a WD significantly reduced plasma total cholesterol and triglycerides (P < 0.0065). In a mouse model of colon cancer metastatic to the lungs, adding 0.06% of Tg6F, but not a control tomato concentrate (EV), to standard mouse chow reduced tumor-associated neutrophils by 94 ± 1.1% (P = 0.0052), and reduced tumor burden by two-thirds (P = 0.0371). Adding 0.06% of either EV or Tg6F by weight to standard mouse chow significantly reduced tumor burden in a mouse model of ovarian cancer; however, Tg6F was significantly more effective (35% reduction for EV vs. 53% reduction for Tg6F; P = 0.0069). Providing the same dose of tomato concentrate to humans would require only two tablespoons three times daily making this a practical approach for testing oral apoA-I mimetic therapy in the treatment of dyslipidemia and cancer. John Wiley & Sons, Ltd 2015-08 2015-06-24 /pmc/articles/PMC4492730/ /pubmed/26171234 http://dx.doi.org/10.1002/prp2.154 Text en © 2015 The Authors. Pharmacology Research & Perspectives published by John Wiley & Sons Ltd, British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Chattopadhyay, Arnab
Grijalva, Victor
Hough, Greg
Su, Feng
Mukherjee, Pallavi
Farias-Eisner, Robin
Anantharamaiah, G M
Faull, Kym F
Hwang, Lin H
Navab, Mohamad
Fogelman, Alan M
Reddy, Srinivasa T
Efficacy of tomato concentrates in mouse models of dyslipidemia and cancer
title Efficacy of tomato concentrates in mouse models of dyslipidemia and cancer
title_full Efficacy of tomato concentrates in mouse models of dyslipidemia and cancer
title_fullStr Efficacy of tomato concentrates in mouse models of dyslipidemia and cancer
title_full_unstemmed Efficacy of tomato concentrates in mouse models of dyslipidemia and cancer
title_short Efficacy of tomato concentrates in mouse models of dyslipidemia and cancer
title_sort efficacy of tomato concentrates in mouse models of dyslipidemia and cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4492730/
https://www.ncbi.nlm.nih.gov/pubmed/26171234
http://dx.doi.org/10.1002/prp2.154
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