The GPR4 antagonist NE-52-QQ57 increases survival, mitigates the hyperinflammatory response and reduces viral load in SARS-CoV-2-infected K18-hACE2 transgenic mice
COVID-19 (Coronavirus disease 19) is caused by infection with SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) in the respiratory system and other organ systems. Tissue injuries resulting from viral infection and host hyperinflammatory responses may lead to moderate to severe pneumonia,...
Saved in:
| Main Authors: | Xin-Jun Wu, Karen A. Oppelt, Ming Fan, Mona A. Marie, Madison M. Swyers, Ashley J. Williams, Isabelle M. Lemasson, Rachel L. Roper, Paul Bolin, Li V. Yang |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2025-07-01
|
| Series: | Frontiers in Pharmacology |
| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fphar.2025.1549296/full |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Comparison of transgenic and adenovirus hACE2 mouse models for SARS-CoV-2 infection
by: Raveen Rathnasinghe, et al.
Published: (2020-01-01) -
The oncogenic roles of GPR176 in ovarian cancer: a molecular target for aggressiveness and gene therapy
by: Ning Yang, et al.
Published: (2024-12-01) -
GPR-TSBiNet: An Information Gradient Enrichment Model for GPR B-Scan Small Target Detection
by: Chongqin Wang, et al.
Published: (2025-04-01) -
The magnetic permeability signature in high-frequency electromagnetic data modeling: a case study for GPR approximation
by: Alejandra I. Sánchez, et al.
Published: (2025-08-01) -
Ogerin induced activation of Gpr68 alters tendon healing
by: Andrew Rodenhouse, et al.
Published: (2025-05-01)