The Journal of Steroid Biochemistry and Molecular Biology, Journal Year: 2024, Volume and Issue: 239, P. 106495 - 106495
Published: Feb. 27, 2024
Language: Английский
The Journal of Steroid Biochemistry and Molecular Biology, Journal Year: 2024, Volume and Issue: 239, P. 106495 - 106495
Published: Feb. 27, 2024
Language: Английский
Nutrients, Journal Year: 2023, Volume and Issue: 15(23), P. 4873 - 4873
Published: Nov. 22, 2023
Ultra-processed foods (UPFs) have gained substantial attention in the scientific community due to their surging consumption and potential health repercussions. In addition well-established poor nutritional profile, UPFs been implicated containing various dietary oxidized sterols (DOxSs). These DOxSs are associated with a spectrum of chronic diseases, including cardiometabolic conditions, cancer, diabetes, Parkinson's, Alzheimer's disease. this study, we present comprehensive database documenting presence other metabolites >60 commonly consumed as part Western diet. Significant differences were found DOxS phytosterol content between ready-to-eat (RTE) fast (FFs). Biomarker analysis revealed that accumulation, particularly 25-OH triol, can potentially discriminate RTEs FFs. This work underscores utility biomarkers early disease detection prevention. However, an essential next step is conducting exposure assessments better comprehend levels association diseases.
Language: Английский
Citations
8Ageing Research Reviews, Journal Year: 2024, Volume and Issue: 101, P. 102475 - 102475
Published: Aug. 31, 2024
Language: Английский
Citations
2Mechanisms of Ageing and Development, Journal Year: 2022, Volume and Issue: 208, P. 111741 - 111741
Published: Sept. 24, 2022
Language: Английский
Citations
11Journal of Lipid Research, Journal Year: 2023, Volume and Issue: 64(12), P. 100479 - 100479
Published: Nov. 20, 2023
Oncosterone (6-oxo-cholestane-3β,5α-diol; OCDO) is an oncometabolite and a tumor promoter on estrogen receptor alpha-positive breast cancer (ER(+) BC) triple-negative cancers (TN BC). OCDO oxysterol formed in three steps from cholesterol: 1) oxygen addition at the double bond to give α- or β- isomers of 5,6-epoxycholestanols (5,6-EC), 2) hydrolyses epoxide ring 5,6-ECs cholestane-3β,5α,6β-triol (CT), 3) oxidation C6 hydroxyl CT OCDO. On other hand, cholesterol can be hydroxylated by CYP27A1 ultimate methyl carbon its side chain 27-hydroxycholesterol ((25R)-Cholest-5-ene-3beta,26-diol, 27HC), which for ER(+) BC. It currently unknown whether precursors position C27 CYP27A1, as impact such modification proliferation TN BC cells. We investigated, herein, 27H-5,6-ECs ((25R)-5,6-epoxycholestan-3β,26-diol), 27H-CT ((25R)-cholestane-3β,5α,6β,26-tetrol) 27H-OCDO ((25R)-cholestane-6-oxo-3β,5α,26-triol) exist metabolites produced cells expressing CYP27A1. report, first time, that these compounds humans. pharmacological genetic evidence responsible their production. Importantly, we found 27-hydroxy-OCDO (27H-OCDO) inhibits cell blocks 27-HC-induced cells, showing this metabolic conversion commutes proliferative properties into antiproliferative ones. These data suggest unprecedented role control carcinogenesis inhibiting activities oncosterone 27-HC.
Language: Английский
Citations
5Advances in experimental medicine and biology, Journal Year: 2023, Volume and Issue: unknown, P. 379 - 400
Published: Dec. 1, 2023
Language: Английский
Citations
4Advances in experimental medicine and biology, Journal Year: 2023, Volume and Issue: unknown, P. 437 - 452
Published: Dec. 1, 2023
Language: Английский
Citations
4Antioxidants, Journal Year: 2024, Volume and Issue: 13(4), P. 435 - 435
Published: April 3, 2024
Down syndrome (DS) is a complex chromosomal disorder considered as genetically determined form of Alzheimer’s disease (AD). Maintenance brain cholesterol homeostasis essential for functioning and development, its dysregulation associated with AD neuroinflammation oxidative damage. Brain imbalances also likely occur in DS, concurring the precocious AD-like neurodegeneration. In this pilot study, we analyzed, Ts2Cje (Ts2) mouse model expression genes encoding key enzymes involved metabolism levels main precursors products (i.e., oxysterols). The results showed, Ts2 mice compared to euploid mice, downregulation transcription 3-hydroxy-3-methylglutaryl-CoA reductase 24-dehydrocholesterol reductase, latter originally recognized an indicator AD, consequent reduction total levels. Moreover, responsible oxidation amounts resulting oxysterols were modified brains, autoxidation increased, suggesting exacerbation cerebral stress. We observed enhanced inflammatory response underlined by upregulation α-interferon interleukin-6, two cytokines whose synthesis increased brains patients. Overall, these suggest that DS share cycle derangements altered oxysterol levels, which may contribute events both diseases.
Language: Английский
Citations
1International Journal of Molecular Sciences, Journal Year: 2024, Volume and Issue: 26(1), P. 77 - 77
Published: Dec. 25, 2024
Oxysterols, as metabolites of cholesterol, play a key role in cholesterol homeostasis, autophagosome formation, and regulation immune responses. Disorders oxysterol metabolism are closely related to the pathogenesis neurodegenerative diseases. To systematically investigate profound molecular regulatory mechanisms diseases, it is necessary quantify oxysterols their central peripheral biospecimens simultaneously accurately. However, there lot unsolved problems with existing methods, such hindrance applying single method different biological specimens or challenge simultaneous quantification due differential groups on ends side chains. Herein, according physicochemical properties structure oxysterols, an optimized liquid chromatography-tandem mass spectrometry for was established by optimizing sample preparation process, chromatographic conditions, mobile phase pH, solvent selection. Seven were detected this method, including 27-hydroxycholesterol, 7α-hydroxycholesterol, 7α,27-dihydroxycholesterol, 7-dehydrocholesterol, 7α-hydroxy-3-oxo-4-cholestenoic acid, 3-hydroxy-5-cholestenoic 24(S)-hydroxycholesterol. Non-derivatization extraction methyl tert-butyl ether used biospecimens, followed separation phenyl hexyl column. By repeated validation, exhibited satisfactory linearity, precision, recovery, sensitivity, repeatability, stability, successfully applied detection plasma, cerebral cortex, liver mouse. In summary, our enables concurrent analysis various presenting broad range applicability.
Language: Английский
Citations
1Bioscience Biotechnology and Biochemistry, Journal Year: 2023, Volume and Issue: 87(4), P. 434 - 441
Published: Jan. 9, 2023
A diet supplemented with cholic acid (CA), the primary 12α-hydroxylated bile acid, can induce hepatic lipid accumulation in rats without obesity. This study examined effects of a CA-supplemented on blood pressure (BP). After acclimation, WKAH/HkmSlc (3 weeks old) were divided into two groups and fed control AIN-93-based or (0.5 g CA/kg) for 13 weeks. The CA increased systolic diastolic BP as well concentrations rats. No changes found sodium concentration. Urinary albumin concentration CA-fed An increase was observed expression ATP-binding cassette subfamily B member 1B that correlated BPs urinary accompanied by an portal taurocholic These results suggest acids are involved albuminuria via alteration function.
Language: Английский
Citations
3The Journal of Steroid Biochemistry and Molecular Biology, Journal Year: 2023, Volume and Issue: 234, P. 106396 - 106396
Published: Sept. 6, 2023
Language: Английский
Citations
3