Lipid metabolism explained

Lipid metabolism is the synthesis and degradation of lipids in cells, involving the breakdown and storage of fats for energy and the synthesis of structural and functional lipids, such as those involved in the construction of cell membranes. In animals, these fats are obtained from food and are synthesized by the liver.[1] Lipogenesis is the process of synthesizing these fats.[2] [3] The majority of lipids found in the human body from ingesting food are triglycerides and cholesterol.[4] Other types of lipids found in the body are fatty acids and membrane lipids. Lipid metabolism is often considered the digestion and absorption process of dietary fat; however, there are two sources of fats that organisms can use to obtain energy: from consumed dietary fats and from stored fat.[5] Vertebrates (including humans) use both sources of fat to produce energy for organs such as the heart to function.[6] Since lipids are hydrophobic molecules, they need to be solubilized before their metabolism can begin. Lipid metabolism often begins with hydrolysis,[7] which occurs with the help of various enzymes in the digestive system. Lipid metabolism also occurs in plants, though the processes differ in some ways when compared to animals.[8] The second step after the hydrolysis is the absorption of the fatty acids into the epithelial cells of the intestinal wall. In the epithelial cells, fatty acids are packaged and transported to the rest of the body.[9]

Metabolic processes include lipid digestion, lipid absorption, lipid transportation, lipid storage, lipid catabolism, and lipid biosynthesis.Lipid catabolism is accomplished by a process known as beta oxidation which takes place in the mitochondria and peroxisome cell organelles.

Lipid digestion

Digestion is the first step to lipid metabolism, and it is the process of breaking the triglycerides down into smaller monoglyceride units with the help of lipase enzymes. Digestion of fats begin in the mouth through chemical digestion by lingual lipase. Ingested cholesterol is not broken down by the lipases and stays intact until it enters the epithelium cells of the small intestine. Lipids then continue to the stomach where chemical digestion continues by gastric lipase and mechanical digestion begins (peristalsis). The majority of lipid digestion and absorption, however, occurs once the fats reach the small intestines. Chemicals from the pancreas (pancreatic lipase family and bile salt-dependent lipase) are secreted into the small intestines to help breakdown the triglycerides,[10] along with further mechanical digestion, until they are individual fatty acid units able to be absorbed into the small intestine's epithelial cells.[11] It is the pancreatic lipase that is responsible for signalling for the hydrolysis of the triglycerides into separate free fatty acids and glycerol units.

Lipid absorption

The second step in lipid metabolism is absorption of fats. Short chain fatty acids can be absorbed in the stomach, while most absorption of fats occurs only in the small intestines. Once the triglycerides are broken down into individual fatty acids and glycerols, along with cholesterol, they will aggregate into structures called micelles. Fatty acids and monoglycerides leave the micelles and diffuse across the membrane to enter the intestinal epithelial cells. In the cytosol of epithelial cells, fatty acids and monoglycerides are recombined back into triglycerides. In the cytosol of epithelial cells, triglycerides and cholesterol are packaged into bigger particles called chylomicrons which are amphipathic structures that transport digested lipids. Chylomicrons will travel through the bloodstream to enter adipose and other tissues in the body.

Lipid transportation

Due to the hydrophobic nature of membrane lipids, triglycerides and cholesterols, they require special transport proteins known as lipoproteins. The amphipathic structure of lipoproteins allows the triglycerides and cholesterol to be transported through the blood. Chylomicrons are one sub-group of lipoproteins which carry the digested lipids from small intestine to the rest of the body. The varying densities between the types of lipoproteins are characteristic to what type of fats they transport.[12] For example, very-low-density lipoproteins (VLDL) carry the triglycerides synthesized by our body and low-density lipoproteins (LDL) transport cholesterol to our peripheral tissues. A number of these lipoproteins are synthesized in the liver, but not all of them originate from this organ.

Lipid storage

Lipids are stored in white adipose tissue as triglycerides. In a lean young adult human, the mass of triglycerides stored represents about 10–20 kilograms. Triglycerides are formed from a backbone of glycerol with three fatty acids. Free fatty acids are activated into acyl-CoA and esterified to finally reach the triglyceride droplet. Lipoprotein lipase has an important role.[13]

Lipid catabolism

Once the chylomicrons (or other lipoproteins) travel through the tissues, these particles will be broken down by lipoprotein lipase in the luminal surface of endothelial cells in capillaries to release triglycerides.[14] Triglycerides will get broken down into fatty acids and glycerol before entering cells and remaining cholesterol will again travel through the blood to the liver.In the cytosol of the cell (for example a muscle cell), the glycerol will be converted to glyceraldehyde 3-phosphate, which is an intermediate in the glycolysis, to get further oxidized and produce energy. However, the main steps of fatty acids catabolism occur in the mitochondria.[15] Long chain fatty acids (more than 14 carbon) need to be converted to fatty acyl-CoA in order to pass across the mitochondria membrane. Fatty acid catabolism begins in the cytoplasm of cells as acyl-CoA synthetase uses the energy from cleavage of an ATP to catalyze the addition of coenzyme A to the fatty acid. The resulting acyl-CoA cross the mitochondria membrane and enter the process of beta oxidation. The main products of the beta oxidation pathway are acetyl-CoA (which is used in the citric acid cycle to produce energy), NADH and FADH. The process of beta oxidation requires the following enzymes: acyl-CoA dehydrogenase, enoyl-CoA hydratase, 3-hydroxyacyl-CoA dehydrogenase, and 3-ketoacyl-CoA thiolase. The diagram to the left shows how fatty acids are converted into acetyl-CoA. The overall net reaction, using palmitoyl-CoA (16:0) as a model substrate is:

7 FAD + 7 NAD+ + 7 CoASH + 7 H2O + H(CH2CH2)7CH2CO-SCoA → 8 CH3CO-SCoA + 7 FADH2 + 7 NADH + 7 H+

Lipid biosynthesis

In addition to dietary fats, storage lipids stored in the adipose tissues are one of the main sources of energy for living organisms.[16] Triacylglycerols, lipid membrane and cholesterol can be synthesized by the organisms through various pathways.

Membrane lipid biosynthesis

There are two major classes of membrane lipids: glycerophospholipids and sphingolipids. Although many different membrane lipids are synthesized in our body, pathways share the same pattern. The first step is synthesizing the backbone (sphingosine or glycerol), the second step is the addition of fatty acids to the backbone to make phosphatidic acid. Phosphatidic acid is further modified with the attachment of different hydrophilic head groups to the backbone. Membrane lipid biosynthesis occurs in the endoplasmic reticulum membrane.[17]

Triglyceride biosynthesis

The phosphatidic acid is also a precursor for triglyceride biosynthesis. Phosphatidic acid phosphotase catalyzes the conversion of phosphatidic acid to diacylglyceride, which will be converted to triglycerides by acyltransferase. Triglyceride biosynthesis occurs in the cytosol.[18]

Fatty acid biosynthesis

The precursor for fatty acids is acetyl-CoA and it occurs in the cytosol of the cell. The overall net reaction, using palmitate (16:0) as a model substrate is:

8 Acetyl-coA + 7 ATP + 14 NADPH + 6H+ → palmitate + 14 NADP+ + 6H2O + 7ADP + 7P¡

Cholesterol biosynthesis

Cholesterol can be made from acetyl-CoA through a multiple-step pathway known as isoprenoid pathway. Cholesterols are essential because they can be modified to form different hormones in the body such as progesterone. 70% of cholesterol biosynthesis occurs in the cytosol of liver cells.

Hormonal regulation of lipid metabolism

Lipid metabolism is tightly regulated by hormones to ensure a balance between energy storage and utilization.

Lipid metabolism disorders

Lipid metabolism disorders (including inborn errors of lipid metabolism) are illnesses where trouble occurs in breaking down or synthesizing fats (or fat-like substances).[21] Lipid metabolism disorders are associated with an increase in the concentrations of plasma lipids in the blood such as LDL cholesterol, VLDL, and triglycerides which most commonly lead to cardiovascular diseases.[22] A good deal of the time these disorders are hereditary, meaning it's a condition that is passed along from parent to child through their genes. Gaucher's disease (types I, II, and III), Niemann–Pick disease, Tay–Sachs disease, and Fabry's disease are all diseases where those afflicted can have a disorder of their body's lipid metabolism.[23] Rarer diseases concerning a disorder of the lipid metabolism are sitosterolemia, Wolman's disease, Refsum's disease, and cerebrotendinous xanthomatosis.

Types of lipids

The types of lipids involved in lipid metabolism include:

Notes and References

  1. News: Overview of Lipid Metabolism. Merck Manuals Professional Edition. 2016-11-01.
  2. Web site: Hydrolysis – Chemistry Encyclopedia – structure, reaction, water, proteins, examples, salt, molecule . chemistryexplained.com . 2016-11-01 .
  3. Book: Freifelder . David . vanc . Molecular biology . 1987 . Jones and Bartlett . Boston . 978-0-86720-069-0 . 2nd . registration .
  4. Book: Baynes . Dominiczak . vanc . Medical Biochemistry . 2014. Saunders, Elsevier Limited. 978-1-4557-4580-7. 121–122.
  5. Arrese EL, Soulages JL . Insect fat body: energy, metabolism, and regulation . Annual Review of Entomology . 55 . 207–25 . 2010 . 19725772 . 3075550 . 10.1146/annurev-ento-112408-085356 .
  6. Book: Lehninger . Albert L . David L. . Nelson . Michael M. . Cox . vanc . Lehninger Principles of Biochemistry . New York . Worth Publishers . 2000 . 3rd . 978-1-57259-931-4 . registration .
  7. Web site: Ophardt . Charles E. . vanc . Lipid Metabolism Summary . 2013 . Virtual Chembook . Elmhurst College .
  8. Wedding RT . May 1972 . Reviewed Work: Plant Lipid Biochemistry . 2430826? . . 71 . 3 . 547–548 .
  9. Jo Y, Okazaki H, Moon YA, Zhao T . Regulation of Lipid Metabolism and Beyond . International Journal of Endocrinology . 2016 . 5415767 . 2016 . 27293434 . 4880713 . 10.1155/2016/5415767 . free .
  10. Book: Pelley . John W. . vanc . Elsevier's Integrated Review Biochemistry . 2012 . Elsevier/Mosby . Philadelphia . 978-0-323-07446-9 . 2nd .
  11. Book: Fundamentals of Biochemistry: Life at the Molecular Level . Donald . Voet . Voet . Judith G. . Pratt . Charlotte W. . vanc . 2013 . Wiley . 978-0-470-54784-7 . Fourth . Hoboken, NJ . 738349533 .
  12. Book: Harris, J. Robin . vanc . 2009 . Cholesterol binding and cholesterol transport proteins: structure and function in health and disease. . Dordrecht . Springer . 978-90-481-8621-1 .
  13. Mechanism of Storage and Synthesis of Fatty Acids and Triglycerides in White Adipocytes | Physiology and Physiopathology of Adipose Tissue pp 101–121 | DOI: 10.1007/978-2-8178-0343-2_8
  14. Book: https://www.ncbi.nlm.nih.gov/books/NBK305896/ . Endotext . Feingold . Kenneth R. . Grunfeld . Carl . vanc . 2000 . MDText.com, Inc.. South Dartmouth (MA) . 26247089 . De Groot . Leslie J. . Chrousos . George . Dungan . Kathleen . Feingold . Kenneth R. . Grossman . Ashley . Hershman . Jerome M. . Koch . Christian . Korbonits . Márta . McLachlan . Robert . Introduction to Lipids and Lipoproteins .
  15. Book: Scheffler IE . Mitochondria . 2008 . Wiley-Liss . Hoboken, N.J. . 978-0-470-04073-7 . 2nd .
  16. Choe SS, Huh JY, Hwang IJ, Kim JI, Kim JB . Adipose Tissue Remodeling: Its Role in Energy Metabolism and Metabolic Disorders . Frontiers in Endocrinology . 7 . 30 . 2016-04-13 . 27148161 . 4829583 . 10.3389/fendo.2016.00030 . free .
  17. Book: Gault CR, Obeid LM, Hannun YA . Sphingolipids as Signaling and Regulatory Molecules . An Overview of Sphingolipid Metabolism: From Synthesis to Breakdown . Advances in Experimental Medicine and Biology . 688 . 1–23 . 2010 . 20919643 . 3069696 . 10.1007/978-1-4419-6741-1_1 . 978-1-4419-6740-4 .
  18. Lok CM, Ward JP, van Dorp DA . The synthesis of chiral glycerides starting from D- and L-serine . Chemistry and Physics of Lipids . 16 . 2 . 115–22 . March 1976 . 1269065 . 10.1016/0009-3084(76)90003-7 .
  19. Sokolova . E. I. . Perova . N. V. . 2004-07-01 . Hormonal Regulation of Lipid Metabolism in Healthy Subjects with or without Obesity . Human Physiology . en . 30 . 4 . 441–444 . 10.1023/B:HUMP.0000036339.26918.92 . 1608-3164.
  20. Zhang . Dengke . Wei . Yanghui . Huang . Qingnan . Chen . Yong . Zeng . Kai . Yang . Weiqin . Chen . Juan . Chen . Jiawei . January 2022 . Important Hormones Regulating Lipid Metabolism . Molecules . en . 27 . 20 . 7052 . 10.3390/molecules27207052 . free . 1420-3049 . 9607181 . 36296646.
  21. News: Lipid Metabolism Disorders. MedlinePlus. 2016-11-20.
  22. Book: O'Malley, Kevin . Clinical Pharmacology and Drug treatment in the elderly . vanc . Churchill Livingstone. 1984. 978-0-443-02297-5. Edinburgh; New York .
  23. News: Disorders of Lipid Metabolism. Merck Manuals Consumer Version. 2016-11-20.
  24. Book: Alberts . Bruce . Johnson . Alexander . Lewis . Julian . Raff . Martin . Roberts . Keith . Walter . Peter . vanc . Molecular Biology of the Cell . 4th . Garland Science . 2002 . 978-0-8153-3218-3 . The Lipid Bilayer . https://www.ncbi.nlm.nih.gov/books/NBK26871/ .
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  26. Russell DW . The enzymes, regulation, and genetics of bile acid synthesis . Annual Review of Biochemistry . 72 . 137–74 . 2003 . 12543708 . 10.1146/annurev.biochem.72.121801.161712 .
  27. Williams KI, Higgs GA . Eicosanoids and Inflammation . The Journal of Pathology . October 1988 . 156 . 2 . 101–110 . 10.1002/path.1711560204 . 3058912 . 34803631 . free .