Abstract
Scope:
The consumption of red and processed meat, and not white meat, associates with the development of various Western diseases such as colorectal cancer and type 2 diabetes. This work aims at unraveling novel meat‐associated mechanisms that are involved in disease development.
Methods and Results:
A non‐hypothesis driven strategy of untargeted metabolomics is applied to assess colon tissue from rats (fed a high dose of beef vs. white meat) and from pigs (fed red/processed meat vs. white meat), receiving a realistic human background diet. An increased carnitine metabolism is observed, which is reflected by higher levels of acylcarnitines and 3‐dehydroxycarnitine (rats and pigs) and trimethylamine‐N‐oxide (rats). While 3‐dehydroxycarnitine is higher in HT29 cells, incubated with colonic beef digests, acylcarnitine levels are reduced. This suggests an altered response from colon cancer cell line towards meat‐induced oxidative stress. Moreover, metabolic differences between rat and pigs are observed in N‐glycolylneuraminic acid incorporation, prostaglandin, and fatty acid synthesis.
Conclusion:
This study demonstrates elevated (acyl)carnitine metabolism in colon tissue of animals that follow a red meat‐based diet, providing mechanistic insights that may aid in explaining the nutritional‐physiological correlation between red/processed meat and Western diseases.
The consumption of red and processed meat, and not white meat, associates with the development of various Western diseases such as colorectal cancer and type 2 diabetes. This work aims at unraveling novel meat‐associated mechanisms that are involved in disease development.
Methods and Results:
A non‐hypothesis driven strategy of untargeted metabolomics is applied to assess colon tissue from rats (fed a high dose of beef vs. white meat) and from pigs (fed red/processed meat vs. white meat), receiving a realistic human background diet. An increased carnitine metabolism is observed, which is reflected by higher levels of acylcarnitines and 3‐dehydroxycarnitine (rats and pigs) and trimethylamine‐N‐oxide (rats). While 3‐dehydroxycarnitine is higher in HT29 cells, incubated with colonic beef digests, acylcarnitine levels are reduced. This suggests an altered response from colon cancer cell line towards meat‐induced oxidative stress. Moreover, metabolic differences between rat and pigs are observed in N‐glycolylneuraminic acid incorporation, prostaglandin, and fatty acid synthesis.
Conclusion:
This study demonstrates elevated (acyl)carnitine metabolism in colon tissue of animals that follow a red meat‐based diet, providing mechanistic insights that may aid in explaining the nutritional‐physiological correlation between red/processed meat and Western diseases.
Original language | English |
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Article number | 2000463 |
Number of pages | 9 |
Journal | Molecular Nutrition & Food Research |
Volume | 65 |
Issue number | 7 |
Early online date | 01 Mar 2021 |
DOIs | |
Publication status | Published - 02 Apr 2021 |
Keywords
- Biotechnology
- Food Science