Affiliations 

  • 1 Department of Pharmacological and Biomolecular Sciences (DiSFeB), Università degli Studi di Milano, Via Balzaretti, 9-20133 Milan, Italy. saba.khalilpour@unimi.it
  • 2 Department of Medical Pharmacology and Physiology, University of Missouri, Columbia, MO 65212, USA. gb3nc@mail.missouri.edu
  • 3 EMAN Biodiscoveries Sdn. Bhd., Suite 126, Level 1, EUREKA Complex, University of Science Malaysia (USM), Minden Gelugor 11800, Penang, Malaysia. fouad@emanbio.com
  • 4 School of Pharmaceutical Sciences, University of Science Malaysia, Minden Gelugor 11800, Penang, Malaysia. edw.mohamed_oday@uoanbar.edu.iq
  • 5 School of Pharmaceutical Sciences, University of Science Malaysia, Minden Gelugor 11800, Penang, Malaysia. jaegan_87@hotmail.com
  • 6 EMAN Biodiscoveries Sdn. Bhd., Suite 126, Level 1, EUREKA Complex, University of Science Malaysia (USM), Minden Gelugor 11800, Penang, Malaysia. tabana@ualberta.ca
  • 7 EMAN Biodiscoveries Sdn. Bhd., Suite 126, Level 1, EUREKA Complex, University of Science Malaysia (USM), Minden Gelugor 11800, Penang, Malaysia. khadeer@emanbio.com
  • 8 Department of Mechanical and Materials Engineering, University of Nebraska-Lincoln, Lincol, NE 68508, USA. atamayol@unl.edu
  • 9 EMAN Biodiscoveries Sdn. Bhd., Suite 126, Level 1, EUREKA Complex, University of Science Malaysia (USM), Minden Gelugor 11800, Penang, Malaysia. aminmalikshah@usm.my
  • 10 Department of Pharmacological and Biomolecular Sciences (DiSFeB), Università degli Studi di Milano, Via Balzaretti, 9-20133 Milan, Italy. enrico.sangiovanni@unimi.it
  • 11 Department of Pharmacological and Biomolecular Sciences (DiSFeB), Università degli Studi di Milano, Via Balzaretti, 9-20133 Milan, Italy. mario.dellagli@unimi.it
  • 12 EMAN Biodiscoveries Sdn. Bhd., Suite 126, Level 1, EUREKA Complex, University of Science Malaysia (USM), Minden Gelugor 11800, Penang, Malaysia. aman.shah@qiup.edu.my
Biomedicines, 2018 Apr 23;6(2).
PMID: 29690612 DOI: 10.3390/biomedicines6020048

Abstract

Modulating oxidative stresses and inflammation can potentially prevent or alleviate the pathological conditions of diseases associated with the nervous system, including ischemic optic neuropathy. In this study we evaluated the anti-neuroinflammatory and neuroprotective activities of Rhus coriaria (R. coriaria) extract in vivo. The half maximal inhibitory concentration (IC50) for DPPH, ABTS and β⁻carotene were 6.79 ± 0.009 µg/mL, 10.94 ± 0.09 µg/mL, and 6.25 ± 0.06 µg/mL, respectively. Retinal ischemia was induced by optic nerve crush injury in albino Balb/c mice. The anti-inflammatory activity of ethanolic extract of R. coriaria (ERC) and linoleic acid (LA) on ocular ischemia was monitored using Fluorescence Molecular Tomography (FMT). Following optic nerve crush injury, the mice treated with 400 mg/kg of ERC and LA exhibited an 84.87% and 86.71% reduction of fluorescent signal (cathepsin activity) respectively. The results of this study provide strong scientific evidence for the neuroprotective activity of the ERC, identifying LA as one of the main components responsible for the effect. ERC may be useful and worthy of further development for its adjunctive utilization in the treatment of optic neuropathy.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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