Natural Product Skatole Ameliorates Lipotoxicity-Induced Multiple Hepatic Damage under Hyperlipidemic Conditions in Hepatocytes
Skatole (3-methylindole, 3MI) is a natural-origin compound derived from plants, insects, and microbial metabolites in human intestines. Skatole has an anti-lipid peroxidation effect and is a biomarker for several diseases. However, its effect on hepatocyte lipid metabolism and lipotoxicity has not b...
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Published in | Nutrients Vol. 15; no. 6; p. 1490 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Abstract | Skatole (3-methylindole, 3MI) is a natural-origin compound derived from plants, insects, and microbial metabolites in human intestines. Skatole has an anti-lipid peroxidation effect and is a biomarker for several diseases. However, its effect on hepatocyte lipid metabolism and lipotoxicity has not been elucidated. Hepatic lipotoxicity is induced by excess saturated free fatty acids in hyperlipidemia, which directly damages the hepatocytes. Lipotoxicity is involved in several metabolic diseases and hepatocytes, particularly affecting nonalcoholic fatty liver disease (NAFLD) progression. NAFLD is caused by the accumulation of fat by excessive free fatty acids (FFAs) in the blood and is accompanied by hepatic damage, such as endoplasmic reticulum (ER) stress, abnormal glucose and insulin metabolism, oxidative stress, and lipoapoptosis with lipid accumulation. Hepatic lipotoxicity causes multiple hepatic damages in NAFLD and has a directly effect on the progression from NAFLD to nonalcoholic steatohepatitis (NASH). This study confirmed that the natural compound skatole improves various damages to hepatocytes caused by lipotoxicity in hyperlipidemic conditions. To induce lipotoxicity, we exposed HepG2, SNU-449, and Huh7 cells to palmitic acid, a saturated fatty acid, and confirmed the protective effect of skatole. Skatole inhibited fat accumulation in the hepatocytes, reduced ER and oxidative stress, and recovered insulin resistance and glucose uptake. Importantly, skatole reduced lipoapoptosis by regulating caspase activity. In conclusion, skatole ameliorated multiple types of hepatocyte damage induced by lipotoxicity in the presence of excess free fatty acids. |
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AbstractList | Skatole (3-methylindole, 3MI) is a natural-origin compound derived from plants, insects, and microbial metabolites in human intestines. Skatole has an anti-lipid peroxidation effect and is a biomarker for several diseases. However, its effect on hepatocyte lipid metabolism and lipotoxicity has not been elucidated. Hepatic lipotoxicity is induced by excess saturated free fatty acids in hyperlipidemia, which directly damages the hepatocytes. Lipotoxicity is involved in several metabolic diseases and hepatocytes, particularly affecting nonalcoholic fatty liver disease (NAFLD) progression. NAFLD is caused by the accumulation of fat by excessive free fatty acids (FFAs) in the blood and is accompanied by hepatic damage, such as endoplasmic reticulum (ER) stress, abnormal glucose and insulin metabolism, oxidative stress, and lipoapoptosis with lipid accumulation. Hepatic lipotoxicity causes multiple hepatic damages in NAFLD and has a directly effect on the progression from NAFLD to nonalcoholic steatohepatitis (NASH). This study confirmed that the natural compound skatole improves various damages to hepatocytes caused by lipotoxicity in hyperlipidemic conditions. To induce lipotoxicity, we exposed HepG2, SNU-449, and Huh7 cells to palmitic acid, a saturated fatty acid, and confirmed the protective effect of skatole. Skatole inhibited fat accumulation in the hepatocytes, reduced ER and oxidative stress, and recovered insulin resistance and glucose uptake. Importantly, skatole reduced lipoapoptosis by regulating caspase activity. In conclusion, skatole ameliorated multiple types of hepatocyte damage induced by lipotoxicity in the presence of excess free fatty acids. |
Audience | Academic |
Author | Hong, Sin-Hyoung Kim, Gun-Hwa Keum, Byeong-Rak Lee, Minji Hong, Yeonhee |
AuthorAffiliation | 1 Division of Research Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, Republic of Korea; hongsi8493@gmail.com (S.-H.H.); hyhbona@naver.com (Y.H.); mmcc0101@naver.com (M.L.); br0104@postech.ac.kr (B.-R.K.) 5 Department of Analytical Science and Technology, Graduate School of Analytical Science and Technology (GRAST), Chungnam National University, Daejeon 34134, Republic of Korea 3 Research Center for Drug Development, CYPHARMA, Daejeon 28119, Republic of Korea 2 Department of Bio-Analytical Science, University of Science and Technology, Daejeon 34113, Republic of Korea 4 Department of Life Sciences, Pohang University of Science and Technology, Pohang 37673, Republic of Korea |
AuthorAffiliation_xml | – name: 4 Department of Life Sciences, Pohang University of Science and Technology, Pohang 37673, Republic of Korea – name: 2 Department of Bio-Analytical Science, University of Science and Technology, Daejeon 34113, Republic of Korea – name: 3 Research Center for Drug Development, CYPHARMA, Daejeon 28119, Republic of Korea – name: 1 Division of Research Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, Republic of Korea; hongsi8493@gmail.com (S.-H.H.); hyhbona@naver.com (Y.H.); mmcc0101@naver.com (M.L.); br0104@postech.ac.kr (B.-R.K.) – name: 5 Department of Analytical Science and Technology, Graduate School of Analytical Science and Technology (GRAST), Chungnam National University, Daejeon 34134, Republic of Korea |
Author_xml | – sequence: 1 givenname: Sin-Hyoung orcidid: 0000-0003-1398-1226 surname: Hong fullname: Hong, Sin-Hyoung organization: Department of Bio-Analytical Science, University of Science and Technology, Daejeon 34113, Republic of Korea – sequence: 2 givenname: Yeonhee surname: Hong fullname: Hong, Yeonhee organization: Division of Research Center for Bioconvergence Analysis, Korea Basic Science Institute, Cheongju 28119, Republic of Korea – sequence: 3 givenname: Minji surname: Lee fullname: Lee, Minji organization: Department of Bio-Analytical Science, University of Science and Technology, Daejeon 34113, Republic of Korea – sequence: 4 givenname: Byeong-Rak surname: Keum fullname: Keum, Byeong-Rak organization: Department of Life Sciences, Pohang University of Science and Technology, Pohang 37673, Republic of Korea – sequence: 5 givenname: Gun-Hwa orcidid: 0000-0003-0360-4435 surname: Kim fullname: Kim, Gun-Hwa organization: Department of Analytical Science and Technology, Graduate School of Analytical Science and Technology (GRAST), Chungnam National University, Daejeon 34134, Republic of Korea |
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Keywords | hepatic damage natural products lipoapoptosis nonalcoholic fatty liver disease lipotoxicity lipid accumulation skatole endoplasmic reticulum stress oxidative stress |
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SubjectTerms | Accumulation Apoptosis Care and treatment Caspase Complications and side effects Cytotoxicity Development and progression Endoplasmic reticulum Endoplasmic Reticulum Stress Fatty Acids - metabolism Fatty Acids, Nonesterified - metabolism Fatty liver Glucose Glucose metabolism Health aspects hepatic damage Hepatocytes Humans Hyperlipidemia Indole Insulin Insulin resistance Intestine Kinases Lipid metabolism Lipid peroxidation Lipids lipoapoptosis lipotoxicity Liver - metabolism Liver diseases Metabolic disorders Metabolites Microorganisms Natural products Non-alcoholic Fatty Liver Disease - metabolism nonalcoholic fatty liver disease Oxidation resistance Oxidative metabolism Oxidative stress Palmitic acid Peroxidation Physiological aspects Phytochemicals Proteins Risk factors skatole Skatole - adverse effects Skatole - metabolism Tumor necrosis factor-TNF |
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Title | Natural Product Skatole Ameliorates Lipotoxicity-Induced Multiple Hepatic Damage under Hyperlipidemic Conditions in Hepatocytes |
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