Notoginsenoside R1-loaded mesoporous silica nanoparticles targeting the site of injury through inflammatory cells improves heart repair after myocardial infarction

• Published in: Redox biology Vol. 54; p. 102384
• Main Authors: Li, Han, Zhu, Jing, Xu, Yan-wu, Mou, Fang-fang, Shan, Xiao-li, Wang, Qiang-li, Liu, Bao-nian, Ning, Ke, Liu, Jia-jia, Wang, Ya-chao, Mi, Jin-xia, Wei, Xiaohui, Shao, Shui-jin, Cui, Guo-hong, Lu, Rong, Guo, Hai-dong
• Format: Journal Article
• Language: English
• Published: Elsevier 01-08-2022
• Subjects: Hippo signaling pathway; MAPK signaling pathway; Mesoporous silica nanoparticles; Myocardial infarction; Notoginsenoside R1; PI3K/AKT signaling pathway; Research Paper
• ISSN: 2213-2317; 2213-2317
• DOI: 10.1016/j.redox.2022.102384

Notoginsenoside R1 (NGR1) is the main monomeric component extracted from the dried roots and rhizomes of Panax notoginseng, and exerts pharmacological action against myocardial infarction (MI). Owing to the differences in compound distribution, absorption, and metabolism
in vivo
, exploring a more effective drug delivery system with a high therapeutic targeting effect is crucial. In the early stages of MI, CD11b-expressing monocytes and neutrophils accumulate at infarct sites. Thus, we designed a mesoporous silica nanoparticle-conjugated CD11b antibody with loaded NGR1 (MSN-NGR1-CD11b antibody), which allowed NGR1 precise targeted delivery to the heart in a noninvasively manner. By increasing targeting to the injured myocardium, intravenous injection of MSN-NGR1-CD11b antibody nanoparticle in MI mice improved cardiac function and angiogenesis, reduced cell apoptosis, and regulate macrophage phenotype and inflammatory factors and chemokines. In order to further explore the mechanism of NGR1 protecting myocardium, cell oxidative stress model and oxygen-glucose deprivation (OGD) model were established. NGR1 protected H9C2 cells and primary cardiomyocytes against oxidative injury induced by H
2
O
2
and OGD treatment. Further network pharmacology and molecular docking analyses suggested that the AKT, MAPK and Hippo signaling pathways were involved in the regulation of NGR1 in myocardial protection. Indeed, NGR1 could elevate the levels of
p
-Akt and
p
-ERK, and promote the nuclear translocation of YAP. Furthermore, LY294002 (AKT inhibitor), U0126 (ERK1/2 inhibitor) and Verteporfin (YAP inhibitor) administration in H9C2 cells indicated the involvement of AKT, MAPK and Hippo signaling pathways in NGR1 effects. Meanwhile, MSN-NGR1-CD11b antibody nanoparticles enhanced the activation of AKT and MAPK signaling pathways and the nuclear translocation of YAP at the infarcted site. Our research demonstrated that MSN-NGR1-CD11b antibody nanoparticle injection after MI enhanced the targeting of NGR1 to the infarcted myocardium and improved cardiac function. More importantly, our pioneering research provides a new strategy for targeting drug delivery systems to the ischemic niche.
NGR1 protected H9C2 cells and primary cardiomyocytes against oxidative injury induced by H
2
O
2
and OGD treatment. MSN-NGR1-CD11b antibody nanoparticle injection after MI enhanced the targeting of NGR1 to the infarcted myocardium and improved cardiac function by activating PIK3/AKT, MAPK/ERK and YAP signaling pathways.
Image 1
•
CD11b antibody modification enhanced the target of Mesoporous silica nanoparticles to injured myocardium.
•
NGR1 promoted the survival of H9C2 against oxidative stress injury through PIK3/AKT, MAPK/ERK and YAP signaling pathways.
•
NGR1 protected neonatal and adult cardiomyocytes from H
2
O
2
and OGD induced oxidative stress damage.
•
MSN-NGR1-CD11b antibody nanoparticles improved heart function by activating PIK3/AKT, MAPK/ERK and YAP signaling pathways.
•
MSN-NGR1-CD11b antibody nanoparticles induced M2 polarization of macrophages and regulated the inflammatory factors.