PMID- 34204966 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20210710 IS - 2076-3921 (Print) IS - 2076-3921 (Electronic) IS - 2076-3921 (Linking) VI - 10 IP - 6 DP - 2021 Jun 3 TI - Protective Effects of Oroxylin A on Retinal Ganglion Cells in Experimental Model of Anterior Ischemic Optic Neuropathy. LID - 10.3390/antiox10060902 [doi] LID - 902 AB - Nonarteritic anterior ischemic optic neuropathy (NAION) is the most common cause of acute vision loss in older people, and there is no effective therapy. The effect of the systemic or local application of steroids for NAION patients remains controversial. Oroxylin A (OA) (5,7-dihydroxy-6-methoxyflavone) is a bioactive flavonoid extracted from Scutellariae baicalensis Georgi. with various beneficial effects, including anti-inflammatory and neuroprotective effects. A previous study showed that OA promotes retinal ganglion cell (RGC) survival after optic nerve (ON) crush injury. The purpose of this research was to further explore the potential actions of OA in ischemic injury in an experimental anterior ischemic optic neuropathy (rAION) rat model induced by photothrombosis. Our results show that OA efficiently attenuated ischemic injury in rats by reducing optic disc edema, the apoptotic death of retinal ganglion cells, and the infiltration of inflammatory cells. Moreover, OA significantly ameliorated the pathologic changes of demyelination, modulated microglial polarization, and preserved visual function after rAION induction. OA activated nuclear factor E2 related factor (Nrf2) signaling and its downstream antioxidant enzymes NAD(P)H:quinone oxidoreductase (NQO-1) and heme oxygenase 1 (HO-1) in the retina. We demonstrated that OA activates Nrf2 signaling, protecting retinal ganglion cells from ischemic injury, in the rAION model and could potentially be used as a therapeutic approach in ischemic optic neuropathy. FAU - Chien, Jia-Ying AU - Chien JY AUID- ORCID: 0000-0002-3438-9435 AD - Institute of Medical Sciences, Tzu Chi University, Hualien 970, Taiwan. FAU - Lin, Shu-Fang AU - Lin SF AD - Institute of Clinical Medicine, National Yang Ming Chiao Tung University, Taipei 112, Taiwan. FAU - Chou, Yu-Yau AU - Chou YY AUID- ORCID: 0000-0001-9030-2173 AD - Department of Molecular Biology and Human Genetics, Tzu Chi University, Hualien 970, Taiwan. FAU - Huang, Chi-Ying F AU - Huang CF AUID- ORCID: 0000-0003-4898-4937 AD - Institute of Clinical Medicine, National Yang Ming Chiao Tung University, Taipei 112, Taiwan. AD - Institute of Biopharmaceutical Sciences, National Yang Ming Chiao Tung University, Taipei 112, Taiwan. FAU - Huang, Shun-Ping AU - Huang SP AD - Institute of Medical Sciences, Tzu Chi University, Hualien 970, Taiwan. AD - Department of Molecular Biology and Human Genetics, Tzu Chi University, Hualien 970, Taiwan. AD - Department of Ophthalmology, Taichung Tzu Chi Hospital, Taichung 472, Taiwan. LA - eng GR - 105-2628-B-320-002-MY3/Ministry of Science and Technology of TAIWAN/ PT - Journal Article DEP - 20210603 PL - Switzerland TA - Antioxidants (Basel) JT - Antioxidants (Basel, Switzerland) JID - 101668981 PMC - PMC8226497 OTO - NOTNLM OT - Nrf2 OT - Oroxylin A OT - ischemic optic neuropathy OT - microglia OT - optical coherence tomography (OCT) OT - oxidative stress OT - retinal ganglion cell OT - visual evoked potential (VEP) COIS- The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results. EDAT- 2021/07/03 06:00 MHDA- 2021/07/03 06:01 PMCR- 2021/06/03 CRDT- 2021/07/02 01:22 PHST- 2021/05/11 00:00 [received] PHST- 2021/05/28 00:00 [revised] PHST- 2021/05/31 00:00 [accepted] PHST- 2021/07/02 01:22 [entrez] PHST- 2021/07/03 06:00 [pubmed] PHST- 2021/07/03 06:01 [medline] PHST- 2021/06/03 00:00 [pmc-release] AID - antiox10060902 [pii] AID - antioxidants-10-00902 [pii] AID - 10.3390/antiox10060902 [doi] PST - epublish SO - Antioxidants (Basel). 2021 Jun 3;10(6):902. doi: 10.3390/antiox10060902.