Bioactivity of Falkenbergia rufolanosa Methanolic Extract: Assessment of Its Effect on Methyl-Thiophanate Induced Bone and Blood Disorders.
Amal FekiIntissar KammounMalek ElerouiRim KallelFatma MegdicheLiwa HarizTahia BoudawaraChoumous KallelHatem KallelJean Marc PujoIbtissem Ben AmaraPublished in: Pharmaceuticals (Basel, Switzerland) (2023)
This study aimed to evaluate the potentiality of a mineral and antioxidant-rich methanolic extract of the red marine alga Falkenbergia rufolanosa (FRE) against methyl-thiophanate (MT)-induced toxicity in adult rats. The animals were allocated into four groups: controls, MT (300 mg/kg), MT + FRE, and FRE-treated group for 7 days. Our results demonstrated severe mineral perturbations due to MT treatment, especially in calcium and phosphorus levels in plasma, urine, and bone. Similarly, the hematological analysis revealed increased red blood cells, platelets, and white blood cells associated with striking genotoxicity. Interestingly, a significant rise in lipid peroxidation and advanced oxidation protein products level in erythrocytes and bone were noted. Meanwhile, a depletion of the antioxidant status in both tissues occurred. These biochemical alterations were in harmony with DNA degradation and histological variation in bone and blood. In the other trend, data showed that treatment with alga improved MT-induced hematotoxicity, genotoxicity, and oxidative stress in the blood and bone. Osteo-mineral metabolism and bone histo-architecture were also noted. In conclusion, these findings demonstrated that the red alga Falkenbergia rufolanosa is a potent source of antioxidant and antibacterial agents, as revealed by the in vitro analysis.
Keyphrases
- oxidative stress
- diabetic rats
- bone mineral density
- anti inflammatory
- soft tissue
- bone loss
- induced apoptosis
- bone regeneration
- high glucose
- red blood cell
- ischemia reperfusion injury
- postmenopausal women
- dna damage
- endothelial cells
- body composition
- early onset
- gene expression
- hydrogen peroxide
- single cell
- single molecule
- nitric oxide
- artificial intelligence
- electronic health record
- young adults
- cell death
- fatty acid