Conjugated fatty 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] The reason why the isomer of conjugated fatty acids are studied is because they have the potential to treat human illnesses.[4] A biological activity that conjugated fatty acids have been studied for is the reduction of body fat and the increasing of lean body mass.[6] There are experimental models that proved the ability of conjugated linoleic acid to reduce fat levels.[7] This is why the scientific community see the potential to use conjugated fatty acids with active treatments to prevent obesity.[6] However, research studies made in humans are in disagreement even though these studies have proven that the supplementation of conjugated linoleic acid has some benefits such as weight loss.[7] On top of the research on conjugated linoleic acid on body weight regulation, isomers of conjugated linoleic acid have been shown in vitro to inhibit the growth and division of a cell to two daughter cells, initiate cell death, and interfere with mutagenicity in human tumor cells.[8]
Conjugated fatty acids can have either a cis or trans configuration. 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.[9] However, CLA’s anti-inflammatory properties correlate to isomer dependence.[10] 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.[10]
See also
References
- 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.
- 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.
- 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.
- 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.
- 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.
- Park, Yeonhwa; Park, Yooheon (January 2012), Patil, Bhimanagouda S.; Jayaprakasha, Guddadarangavvanahally K.; Murthy, Kotamballi N. Chidambara; Seeram, Navindra P. (eds.), "Conjugated Fatty Acids as a Prevention Tool for Obesity and Osteoporosis", Emerging Trends in Dietary Components for Preventing and Combating Disease, American Chemical Society, vol. 1093, pp. 393–405, doi:10.1021/bk-2012-1093.ch022, ISBN 978-0-8412-2664-7
- Lehnen, Tatiana Ederich; da Silva, Marcondes Ramos; Camacho, Augusto; Marcadenti, Aline; Lehnen, Alexandre Machado (December 2015). "A review on effects of conjugated linoleic fatty acid (CLA) upon body composition and energetic metabolism". Journal of the International Society of Sports Nutrition. 12 (1): 36. doi:10.1186/s12970-015-0097-4. ISSN 1550-2783. PMC 4574006. PMID 26388708.
- Ferlay, Anne; Bernard, Laurence; Meynadier, Annabelle; Malpuech-Brugère, Corinne (2017-10-01). "Production of trans and conjugated fatty acids in dairy ruminants and their putative effects on human health: A review". Biochimie. 141: 107–120. doi:10.1016/j.biochi.2017.08.006. ISSN 0300-9084. PMID 28804001.
- 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.
- 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.