Chemical structure of the conjugated fatty acid rumenic acid, an isomer of conjugated linoleic acid

Conjugated fatty acids is jargon for polyunsaturated fatty acids containing at least one pair of conjugated double bonds.[1] An example of a conjugated fatty acid is the rumenic acid, found in the meat and milk of ruminants. Most unsaturated fatty acids that are doubly unsaturated do not feature conjugation, e.g., linoleic acid and linoelaidic acid.

Some conjugated fatty acids may confer health benefits ranging from the prevention of hypertension to protection against certain forms of cancer, although more research is needed to confirm such effects.[2] Clinical studies and animal models have shown that conjugated fatty acids confer physiological benefits such as the regulation of the synthesis and breakdown of lipids, reduction of inflammation, and antioxidant properties.[3]

Conjugated fatty acids include isomers of linoleic acid.[4] Conjugated analogues linoleic acids are the most investigated conjugated fatty acids.[5]

Some conjugated fatty acids feature trans alkenes. For instance, the rumenic acid (cis-9, trans-11) is a conjugated trans fatty acid.

Studies have suggested that conjugated linoleic acids, an isomer of conjugated fatty acids, can modulate inflammatory responses in the body.[6] However, CLA’s anti-inflammatory properties correlate to isomer dependence.[7] For instance, (cis-9, trans-11) CLA has been shown to have a decreased inflammatory effect on adipose tissues of mice with obesity-causing genes, while (trans-10, cis-12) CLA reduces obesity in mice without affecting insulin resistance or adipose tissue inflammation.[7]

See also

References

  1. ^ Rawat, Richa; Yu, Xiao-Hong; Sweet, Marie; Shanklin, John (26 March 2012). "Conjugated Fatty Acid Synthesis". Journal of Biological Chemistry. 287 (20): 16230–16237. doi:10.1074/jbc.M111.325316. PMC 3351362. PMID 22451660.
  2. ^ Nagao, K; Yanagita, T (2005). "Conjugated fatty acids in food and their health benefits". Journal of Bioscience and Bioengineering. 100 (2): 152–7. doi:10.1263/jbb.100.152. PMID 16198256.
  3. ^ Gong, Mengyue; Hu, Yulin; Wei, Wei; Jin, Qingzhe; Wang, Xingguo (2019-12-01). "Production of conjugated fatty acids: A review of recent advances". Biotechnology Advances. 37 (8): 107454. doi:10.1016/j.biotechadv.2019.107454. ISSN 0734-9750. PMID 31639444. S2CID 204849936.
  4. ^ Hennessy, Alan A.; Ross, Paul R.; Fitzgerald, Gerald F.; Stanton, Catherine (April 2016). "Sources and Bioactive Properties of Conjugated Dietary Fatty Acids". Lipids. 51 (4): 377–397. doi:10.1007/s11745-016-4135-z. ISSN 0024-4201. PMID 26968402. S2CID 3941392.
  5. ^ Gong, Mengyue; Hu, Yulin; Wei, Wei; Jin, Qingzhe; Wang, Xingguo (2019-12-01). "Production of conjugated fatty acids: A review of recent advances". Biotechnology Advances. 37 (8): 107454. doi:10.1016/j.biotechadv.2019.107454. ISSN 0734-9750. PMID 31639444. S2CID 204849936.
  6. ^ Park, Yeonhwa (January 2009). "Conjugated linoleic acid (CLA): Good or bad trans fat?". Journal of Food Composition and Analysis. 22: S4–S12. doi:10.1016/j.jfca.2008.12.002.
  7. ^ a b Yuan, Gaofeng; Chen, Xiaoe; Li, Duo (2015-02-25). "Modulation of Peroxisome Proliferator-Activated Receptor gamma (PPAR γ) by Conjugated Fatty Acid in Obesity and Inflammatory Bowel Disease". Journal of Agricultural and Food Chemistry. 63 (7): 1883–1895. doi:10.1021/jf505050c. ISSN 0021-8561. PMID 25634802.
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