Aloe juvenna Brandham & S.Carter as α-Amylase Inhibitor and Hypoglycaemic Agent with Anti-inflammatory Properties for Diabetes Management.
Mona Abd El-Mouty RaslanIman AbdelKhalek AbdelKhalek KassemNeveen Sabry GhalyMay Aly El-ManawatyFarouk Rasmy MelekMarian NabilPublished in: Chemistry & biodiversity (2024)
Despite Aloe's traditional use, Aloe juvenna Brandham & S.Carter is poorly characterized. Other Aloes are known for their antidiabetic activity. This study describes the antidiabetic potentials and phytoconstituents of the A. juvenna leaves methanolic extract (AJME). Twenty-six phytoconstituents of AJME were described using HPLC/MS-MS. Lupeol and vitexin were isolated using column chromatography. The antidiabetic activity of AJME was investigated using an in vivo high-fat diet/streptozotocin-induced diabetic rat model and in vitro α-glucosidase and α-amylase inhibitory activity assays. AJME demonstrated its α-amylase inhibitory activity (IC 50 =313±39.9 ppm) with no effect on α-glucosidase. In vivo, AJME dose-dependently improved hyperglycaemia in a high-fat diet/streptozotocin-induced diabetic rat model. Notably, the higher dose (1600 mg/kg) of AJME significantly downregulated serum interleukin-6, tumor necrosis factor-α, and matrix metalloproteinase-1 genes, suggesting its anti-inflammatory effect. These findings indicate AJME's potential as a significant antidiabetic agent through its α-amylase inhibition, hypoglycaemic, and anti-inflammatory properties.
Keyphrases
- high fat diet
- anti inflammatory
- ms ms
- insulin resistance
- adipose tissue
- diabetic rats
- type diabetes
- high glucose
- mass spectrometry
- oxidative stress
- high performance liquid chromatography
- liquid chromatography
- tandem mass spectrometry
- cardiovascular disease
- solid phase extraction
- wound healing
- simultaneous determination
- high speed
- drug induced
- skeletal muscle
- metabolic syndrome
- liquid chromatography tandem mass spectrometry
- atomic force microscopy
- risk assessment
- ultra high performance liquid chromatography
- stress induced
- diabetic nephropathy
- genome wide analysis