Efficacy of Clinically Used PARP Inhibitors in a Murine Model of Acute Lung Injury

• Published in: Cells (Basel, Switzerland) Vol. 11; no. 23; p. 3789
• Main Authors: Martins, Vanessa, Santos, Sidneia S, Rodrigues, Larissa de O C P, Salomao, Reinaldo, Liaudet, Lucas, Szabo, Csaba
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 26-11-2022; MDPI
• Subjects: Acute Lung Injury - drug therapy; Animal models; Animals; Apoptosis; Caspase-3; Cell culture; cell death; cytokines; Disease Models, Animal; DNA damage; Dosage and administration; Drug therapy; Enzyme inhibitors; Epithelial cells; Extravasation; Humans; Inflammasomes; Inflammation; Inflammation Mediators - pharmacology; Laboratory animals; Lavage; Lung; Lung diseases; Lungs; Mice; Monocytes; Necrosis; NF-κB protein; olaparib; Patient outcomes; Poly(ADP-ribose); Poly(ADP-ribose) polymerase; Poly(ADP-ribose) Polymerase Inhibitors - pharmacology; Poly(ADP-ribose) Polymerase Inhibitors - therapeutic use; Ribose; Switzerland; United States > US; Basel Switzerland; cytokines; cell death; inflammation; olaparib
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells11233789

Poly(ADP-ribose) polymerase 1 (PARP1), as a potential target for the experimental therapy of acute lung injury (ALI), was identified over 20 years ago. However, clinical translation of this concept was not possible due to the lack of clinically useful PARP inhibitors. With the clinical introduction of several novel, ultrapotent PARP inhibitors, the concept of PARP inhibitor repurposing has re-emerged. Here, we evaluated the effect of 5 clinical-stage PARP inhibitors in oxidatively stressed cultured human epithelial cells and monocytes in vitro and demonstrated that all inhibitors (1-30 µM) provide a comparable degree of cytoprotection. Subsequent in vivo studies using a murine model of ALI compared the efficacy of olaparib and rucaparib. Both inhibitors (1-10 mg/kg) provided beneficial effects against lung extravasation and pro-inflammatory mediator production-both in pre- and post-treatment paradigms. The underlying mechanisms include protection against cell dysfunction/necrosis, inhibition of NF-kB and caspase 3 activation, suppression of the NLRP3 inflammasome, and the modulation of pro-inflammatory mediators. Importantly, the efficacy of PARP inhibitors was demonstrated without any potentiation of DNA damage, at least as assessed by the TUNEL method. These results support the concept that clinically approved PARP inhibitors may be repurposable for the experimental therapy of ALI.