Healthy Properties of a New Formulation of Pomegranate-Peel Extract in Mice Suffering from Experimental Autoimmune Encephalomyelitis.
Giulia VallarinoAnnalisa SalisElena LucariniFederica TurriniGuendalina OliveroAlessandra RoggeriGianluca DamonteRaffaella BoggiaDi Cesare Mannelli LorenzoCarla GhelardiniAnna PittalugaPublished in: Molecules (Basel, Switzerland) (2022)
A new formulation of a pomegranate-peel extract (PEm) obtained by PUAE (Pulsed Ultrasound-Assisted Extraction) and titrated in both ellagic acid (EA) and punicalagin is proposed, characterized and then analyzed for potential health properties in mice suffering from the experimental autoimmune encephalomyelitis (EAE). PEm effects were compared to those elicited by a formulation containing EA (EAm). Control and EAE mice were chronically administered EAm and Pem dissolved in the drinking water, starting from the day 10 post-immunization (d.p.i.), with a "therapeutic" protocol to deliver daily 50 mg/kg of EA. Treated EAE mice did not limit their daily access to the beverage, nor did they show changes in body weight, but they displayed a significant amelioration of "in vivo" clinical symptoms. "Ex vivo" histochemical analysis showed that spinal-cord demyelination and inflammation in PEm and EAm-treated EAE mice at 23 ± 1 d.p.i. were comparable to those in the untreated EAE animals, while microglia activation (measured as Ionized Calcium Binding Adaptor 1, Iba1 staining) and astrocytosis (quantified as glial fibrillar acid protein, GFAP immunopositivity) significantly recovered, particularly in the gray matter. EAm and PEm displayed comparable efficiencies in controlling the spinal pathological cellular hallmarks in EAE mice, and this would support their delivery as dietary supplementation in patients suffering from multiple sclerosis (MS).
Keyphrases
- high fat diet induced
- multiple sclerosis
- spinal cord
- body weight
- drug delivery
- oxidative stress
- randomized controlled trial
- neuropathic pain
- public health
- insulin resistance
- newly diagnosed
- spinal cord injury
- inflammatory response
- wild type
- mental health
- metabolic syndrome
- ms ms
- chronic kidney disease
- binding protein
- small molecule
- amino acid
- protein protein