The search for new therapeutic approaches to Alzheimer disease (AD) is a major goal in medicine and society, also due to the impressive economic and social costs of this disease. In this scenario, biotechnologies play an important role. Here, it is demonstrated that the Radio Electric Asymmetric Conveyer (REAC), an innovative technology platform for neuro- and bio-modulation, used according to the neuro-regenerative protocol (RGN-N), significantly increases astroglial reaction around the amyloid plaques in an AD mouse model, as evaluated by GFAP-immunoreactivity, and reduces microglia-associated neuroinflammation markers, as evaluated by Iba1-immunoreactivity and mRNA expression level of inflammatory cytokines TREM. IL1beta, iNOS and MRC1 were not affected neither by the genotype or by REAC RGN-N treatment. Also observed was an increase in locomotion in treated animals. The study was performed in 24-month-old male Tg2576 mice and age-matching wild-type animals, tested for Y-maze, contextual fear conditioning and locomotion immediately after the end of a specific REAC treatment administered for 15 hours/day for 15 days. These results demonstrated that REAC RGN-N treatment modifies pathological neuroinflammation, and mitigates part of the complex motor behaviour alterations observed in very old Tg2576 mice.

REAC technology modifies pathological neuroinflammation and motor behaviour in an Alzheimer's disease mouse model / Lorenzini, Luca; Giuliani, Alessandro; Sivilia, Sandra; Baldassarro, VITO ANTONIO; FERNANDEZ CANALES, MARIA DE LAS MERCEDES; Lotti Margotti, M.; Giardino, Luciana; Fontani, V.; Rinaldi, S.; Calza', Laura. - In: SCIENTIFIC REPORTS. - ISSN 2045-2322. - ELETTRONICO. - 6:(2016), pp. 35719.1-35719.10. [10.1038/srep35719]

REAC technology modifies pathological neuroinflammation and motor behaviour in an Alzheimer's disease mouse model.

LORENZINI, LUCA;GIULIANI, ALESSANDRO;SIVILIA, SANDRA;BALDASSARRO, VITO ANTONIO;FERNANDEZ CANALES, MARIA DE LAS MERCEDES;GIARDINO, LUCIANA;CALZA', LAURA
2016

Abstract

The search for new therapeutic approaches to Alzheimer disease (AD) is a major goal in medicine and society, also due to the impressive economic and social costs of this disease. In this scenario, biotechnologies play an important role. Here, it is demonstrated that the Radio Electric Asymmetric Conveyer (REAC), an innovative technology platform for neuro- and bio-modulation, used according to the neuro-regenerative protocol (RGN-N), significantly increases astroglial reaction around the amyloid plaques in an AD mouse model, as evaluated by GFAP-immunoreactivity, and reduces microglia-associated neuroinflammation markers, as evaluated by Iba1-immunoreactivity and mRNA expression level of inflammatory cytokines TREM. IL1beta, iNOS and MRC1 were not affected neither by the genotype or by REAC RGN-N treatment. Also observed was an increase in locomotion in treated animals. The study was performed in 24-month-old male Tg2576 mice and age-matching wild-type animals, tested for Y-maze, contextual fear conditioning and locomotion immediately after the end of a specific REAC treatment administered for 15 hours/day for 15 days. These results demonstrated that REAC RGN-N treatment modifies pathological neuroinflammation, and mitigates part of the complex motor behaviour alterations observed in very old Tg2576 mice.
2016
REAC technology modifies pathological neuroinflammation and motor behaviour in an Alzheimer's disease mouse model / Lorenzini, Luca; Giuliani, Alessandro; Sivilia, Sandra; Baldassarro, VITO ANTONIO; FERNANDEZ CANALES, MARIA DE LAS MERCEDES; Lotti Margotti, M.; Giardino, Luciana; Fontani, V.; Rinaldi, S.; Calza', Laura. - In: SCIENTIFIC REPORTS. - ISSN 2045-2322. - ELETTRONICO. - 6:(2016), pp. 35719.1-35719.10. [10.1038/srep35719]
Lorenzini, Luca; Giuliani, Alessandro; Sivilia, Sandra; Baldassarro, VITO ANTONIO; FERNANDEZ CANALES, MARIA DE LAS MERCEDES; Lotti Margotti, M.; Giardino, Luciana; Fontani, V.; Rinaldi, S.; Calza', Laura
File in questo prodotto:
File Dimensione Formato  
Scientific Reports.pdf

accesso aperto

Tipo: Versione (PDF) editoriale
Licenza: Licenza per Accesso Aperto. Creative Commons Attribuzione (CCBY)
Dimensione 1.11 MB
Formato Adobe PDF
1.11 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/596715
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 13
  • ???jsp.display-item.citation.isi??? 14
social impact