Citrullus mucosospermus Extract Exerts Protective Effects against Methionine- and Choline-Deficient Diet-Induced Nonalcoholic Steatohepatitis in Mice.
Sun Young ParkJi Eun KimHye Mi KangKi Ho ParkByoung Il JeKi Won LeeDae Youn HwangYoung Whan ChoiPublished in: Foods (Basel, Switzerland) (2024)
In recent years, there has been increasing interest in exploring the potential therapeutic advantages of Citrullus mucosospermus extracts (CME) for nonalcoholic steatohepatitis (NASH). In this study, we investigated the therapeutic effects of CME on NASH using a mice model. High-performance liquid chromatography (HPLC) was employed to identify cucurbitacin E and cucurbitacin E-2-O-glucoside from the CME. Although CME did not significantly alter the serum lipid levels in methionine- and choline-deficient (MCD) mice, it demonstrated a protective effect against MCD diet-induced liver damage. CME reduced histological markers, reduced alanine transaminase (ALT) and aspartame transaminase (AST) levels, and modulated key NASH-related genes, including C/EBPα , PPARγ , Fas , and aP2 . In addition, CME was found to restore hormone-sensitive lipase ( HSL ) and adipose triglyceride lipase ( ATGL ) activity, both crucial for fat catabolism, and reduced the levels of pro-inflammatory cytokines. Furthermore, CME demonstrated the potential to mitigate oxidative stress by maintaining or enhancing the activation and expression of nuclear factor erythroid 2-related factor 2 ( Nrf2 ) and superoxide dismutase ( SOD ), both pivotal players in antioxidant defense mechanisms. These findings underscore the promising therapeutic potential of CME in ameliorating liver damage, inflammation, and oxidative stress associated with NASH.
Keyphrases
- oxidative stress
- high performance liquid chromatography
- nuclear factor
- dna damage
- diabetic rats
- ischemia reperfusion injury
- induced apoptosis
- mass spectrometry
- adipose tissue
- tandem mass spectrometry
- poor prognosis
- fatty acid
- wild type
- ms ms
- type diabetes
- toll like receptor
- transcription factor
- nitric oxide
- binding protein
- amino acid
- immune response
- metabolic syndrome
- endoplasmic reticulum stress
- liquid chromatography
- long non coding rna
- high speed