Aphanizomenon flos-aquae (AFA) Extract Prevents Neurodegeneration in the HFD Mouse Model by Modulating Astrocytes and Microglia Activation.
Giacoma GalizziIrene DeiddaAntonella AmatoPasquale CalviSimona TerzoLuca CaruanaStefano ScoglioFlavia MulèMarta Di CarloPublished in: International journal of molecular sciences (2023)
Obesity and related metabolic dysfunctions are associated with neurodegenerative diseases, such as Alzheimer's disease. Aphanizomenon flos-aquae (AFA) is a cyanobacterium considered a suitable supplement for its nutritional profile and beneficial properties. The potential neuroprotective effect of an AFA extract, commercialized as KlamExtra ® , including the two AFA extracts Klamin ® and AphaMax ® , in High-Fat Diet (HFD)-fed mice was explored. Three groups of mice were provided with a standard diet (Lean), HFD or HFD supplemented with AFA extract (HFD + AFA) for 28 weeks. Metabolic parameters, brain insulin resistance, expression of apoptosis biomarkers, modulation of astrocytes and microglia activation markers, and Aβ deposition were analyzed and compared in the brains of different groups. AFA extract treatment attenuated HFD-induced neurodegeneration by reducing insulin resistance and loss of neurons. AFA supplementation improved the expression of synaptic proteins and reduced the HFD-induced astrocytes and microglia activation, and Aβ plaques accumulation. Together, these outcomes indicate that regular intake of AFA extract could benefit the metabolic and neuronal dysfunction caused by HFD, decreasing neuroinflammation and promoting Aβ plaques clearance.
Keyphrases
- high fat diet
- insulin resistance
- high fat diet induced
- oxidative stress
- adipose tissue
- metabolic syndrome
- skeletal muscle
- diabetic rats
- type diabetes
- mouse model
- polycystic ovary syndrome
- inflammatory response
- poor prognosis
- cerebral ischemia
- anti inflammatory
- neuropathic pain
- high glucose
- weight loss
- traumatic brain injury
- cell death
- risk assessment
- multiple sclerosis
- brain injury
- lps induced
- climate change
- combination therapy
- spinal cord injury
- bone mineral density
- endothelial cells
- functional connectivity