Protective effects of Colomast®, A New Formulation of Adelmidrol and Sodium Hyaluronate, in A Mouse Model of Acute Restraint Stress.
Ramona D'amicoRosalba SiracusaRoberta FuscoMarika CordaroTiziana GenoveseAlessio Filippo PeritoreEnrico GugliandoloRosalia CrupiDaniela ImpellizzeriSalvatore CuzzocreaRosanna Di PaolaPublished in: International journal of molecular sciences (2020)
Stress is generally defined as a homeostatic disruption from actual or implied threats and alters the homeostatic balance of different body organs, such as gastrointestinal function and the hypothalamic-pituitary-adrenal axis (HPA), inducing the release of glucocorticoid hormones. Stress is also known to be a risk factor for the development of depression and anxiety. However, until today there are no suitable therapies for treating of stress. The aim of this study was to explore the protective effect of Colomast®, a new preparation containing Adelmidrol, an enhancer of physiological of palmitoylethanolamide (PEA), and sodium hyaluronate in an animal model of immobilization stress. Acute restraint stress (ARS) was induced in mice by fixation for 2 h of the four extremities with an adhesive tape and Colomast® (20 mg/kg) was administered by oral gavage 30 min before the immobilization. Colomast® pre-treatment was able to decrease histopathological changes in the gastrointestinal tract, cytokines expression, neutrophil infiltration, mast cell activation, oxidative stress, as well as modulate nuclear factor NF-kB and apoptosis pathways after ARS induction. Moreover, Colomast® was able to restore tight junction in both ileum and hippocampus and cortex. Additionally, we demonstrated that Colomast® ameliorated depression and anxiety-related behaviours, and modulate inflammatory and apoptosis pathways also in brain after ARS induction. In conclusion, our results suggest Colomast® to be a potential approach to ARS.
Keyphrases
- oxidative stress
- stress induced
- nuclear factor
- mouse model
- diabetic rats
- liver failure
- endoplasmic reticulum stress
- drug induced
- binding protein
- type diabetes
- cell cycle arrest
- minimally invasive
- blood brain barrier
- functional connectivity
- multiple sclerosis
- poor prognosis
- resting state
- respiratory failure
- heat stress
- metabolic syndrome
- pi k akt
- extracorporeal membrane oxygenation
- cell proliferation
- risk assessment
- brain injury
- combination therapy
- cognitive impairment
- climate change
- immune response
- mass spectrometry
- aortic dissection
- subarachnoid hemorrhage
- acute respiratory distress syndrome
- solid phase extraction
- magnetic nanoparticles
- soft tissue
- prefrontal cortex