PMID- 34462642 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20210901 IS - 1741-427X (Print) IS - 1741-4288 (Electronic) IS - 1741-427X (Linking) VI - 2021 DP - 2021 TI - The RIG-I Signal Pathway Mediated Panax notoginseng Saponin Anti-Inflammatory Effect in Ischemia Stroke. PG - 8878428 LID - 10.1155/2021/8878428 [doi] LID - 8878428 AB - Panax notoginseng saponins (PNS), the main bioactive constituents of a traditional Chinese herb Panax notoginseng, were commonly used for ischemic stroke in China. However, the associated cellular and molecular mechanisms of PNS have not been well examined. This study aimed to decipher the underlying molecular target of PNS in the treatment of cerebral ischemia. The oxygen-glucose-deprived (OGD) model of rat brain microvascular endothelial cells (BMECs) was used in this study. The alteration of gene expression in rat BMECs after PNS treatment was measured by microarray and indicated that there were 38 signaling pathways regulated by PNS. Among them, RIG-I receptor and related signaling molecules TNF receptor-associated factor 2 (Traf2) and nuclear factor-kappa B (NF-kappaB) were significantly suppressed by PNS, which was verified again in OGD-induced BMECs measured by FQ-PCR and western blotting and in middle cerebral artery occlusion (MCAO) rats measured by immunohistochemistry. The levels of TNF-alpha, IL-8, and the downstream cytokines regulated by RIG-I receptor pathway were also decreased by PNS. Meanwhile, the neurological evaluation, hematoxylin and eosin (HE) staining, and Evans blue staining were conducted to evaluate the effect of PNS in MCAO rats. Results showed PNS significantly improved functional outcome and cerebral vascular leakage. Flow cytometry showed the number of the inflammatory cells infiltrated in brain tissue was decreased in PNS treatment. Our results identified that RIG-I signaling pathway mediated anti-inflammatory properties of PNS in cerebral ischemia, which provided the novel insights of PNS application in clinics. CI - Copyright (c) 2021 Chujun Zhang et al. FAU - Zhang, Chujun AU - Zhang C AD - School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China. AD - Nanchang Hongdu Hospital of Traditional Chinese Medicine, Nanchang, China. FAU - Zhang, Sai AU - Zhang S AD - School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China. FAU - Wang, Lanxiang AU - Wang L AD - Department of Traditional Chinese Medicine, The 8th Medical Center of Chinese PLA General Hospital, Beijing, China. FAU - Kang, Soyeon AU - Kang S AD - School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China. FAU - Ma, Jiabao AU - Ma J AD - School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China. FAU - Liu, Shihao AU - Liu S AD - Department of Cell and Developmental Biology, School of Molecular and Cellular Biology, University of Illinois at Urbana-Champaign, USA. FAU - Hu, Yanhong AU - Hu Y AD - School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China. FAU - Zhang, Fan AU - Zhang F AD - School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China. FAU - Sun, Tianshi AU - Sun T AD - School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China. FAU - Dong, Yixin AU - Dong Y AD - School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China. FAU - Li, Tenghui AU - Li T AD - School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China. FAU - Li, Weihong AU - Li W AUID- ORCID: 0000-0002-8047-8201 AD - School of Nursing, Beijing University of Chinese Medicine, Beijing, China. FAU - Du, Qinghong AU - Du Q AUID- ORCID: 0000-0002-3753-5995 AD - School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China. AD - Institute of Tibetan Medicine, University of Tibetan Medicine, Lhasa, China. LA - eng PT - Journal Article DEP - 20210820 PL - United States TA - Evid Based Complement Alternat Med JT - Evidence-based complementary and alternative medicine : eCAM JID - 101215021 PMC - PMC8403041 COIS- The authors declare no conflicts of interest. EDAT- 2021/09/01 06:00 MHDA- 2021/09/01 06:01 PMCR- 2021/08/20 CRDT- 2021/08/31 06:39 PHST- 2020/09/07 00:00 [received] PHST- 2021/02/09 00:00 [revised] PHST- 2021/08/07 00:00 [accepted] PHST- 2021/08/31 06:39 [entrez] PHST- 2021/09/01 06:00 [pubmed] PHST- 2021/09/01 06:01 [medline] PHST- 2021/08/20 00:00 [pmc-release] AID - 10.1155/2021/8878428 [doi] PST - epublish SO - Evid Based Complement Alternat Med. 2021 Aug 20;2021:8878428. doi: 10.1155/2021/8878428. eCollection 2021.