S‐Methyl Cysteine Sulfoxide Does Not Ameliorate Weight Gain or Hyperlipidemia in Mice Fed a High‐Fat Diet

Author:

Hill Caroline R.1ORCID,Shafaei Armaghan2,Matthews Vance B.3,Ward Natalie C.4,Croft Kevin D.5,Lewis Joshua R.167,Hodgson Jonathan M.16,Balmer Lois89,Blekkenhorst Lauren C.16

Affiliation:

1. Nutrition and Health Innovation Research Institute School of Medical and Health Science Royal Perth Hospital Research Foundation Edith Cowan University Perth Western Australia 6000 Australia

2. Centre for Integrative Metabolomics and Computational Biology School of Science Edith Cowan University Joondalup Australia Western Australia 6027

3. Dobney Hypertension Centre School of Biomedical Science, Royal Perth Hospital Unit Royal Perth Hospital Medical Research Foundation University of Western Australia Perth Western Australia 6000 Australia

4. Dobney Hypertension Centre Medical School, Royal Perth Hospital Unit Royal Perth Hospital Medical Research Foundation University of Western Australia Perth Western Australia 6000 Australia

5. School of Biomedical Science Royal Perth Hospital Unit University of Western Australia Perth Western Australia 6000 Australia

6. Medical School University of Western Australia Perth Western Australia 6000 Australia

7. Centre for Kidney Research Children's Hospital at Westmead School of Public Health Sydney Medical School The University of Sydney Sydney New South Wales 2000 Australia

8. Centre for Diabetes Research Harry Perkins Institute for Medical Research Nedlands Western Australia 6009 Australia

9. Centre for Precision Health School of Medical and Health Science Edith Cowan University Joondalup Western Australia Australia 6027

Abstract

ScopeHigher intake of cruciferous and allium vegetables is associated with lower cardiometabolic risk. Little research has investigated the cardiometabolic effects of S‐methyl cysteine sulfoxide (SMCSO), found abundant in these vegetables. This study hypothesizes that SMCSO will blunt development of metabolic syndrome features in mice fed high‐fat feed.Methods and resultsFifty C57BL/6 male mice are randomly assigned to standard‐chow, high‐fat, or high‐fat supplemented with low‐SMCSO (43 mg kg−1 body weight [BW] day−1), medium‐SMCSO (153 mg kg−1 BW day−1), or high‐SMCSO (256 mg kg−1 BW day−1) for 12‐weeks. High‐fat with SMCSO did not prevent diet‐induced obesity, glucose intolerance, or hypercholesterolemia. Mice fed high‐fat with SMCSO has higher hepatic lipids than mice fed standard‐chow or high‐fat alone. Urinary SMCSO increases at 6‐ and 12‐weeks in the low‐SMCSO group, before reducing 46% and 28% in the medium‐ and high‐SMCSO groups, respectively, at 12‐weeks, suggesting possible tissue saturation. Interestingly, two SMCSO‐fed groups consume significantly more feed, without significant weight gain. Due to limitations in measuring consumed feed, caution should be taken interpreting these results.ConclusionSMCSO (43–256 mg kg−1 BW day−1) does not ameliorate metabolic syndrome features in high‐fat fed mice. Substantial knowledge gaps remain. Further studies should administer SMCSO separately (i.e., gavage), with metabolic studies exploring tissue levels to better understand its physiological action.

Publisher

Wiley

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