Abstract |
Pulmonary fibrosis is an irreversible lung disorder with predictable decline in lung function leading to respiratory insufficiency. Incidence of pulmonary fibrosis has been apparently increasing worldwide. Though aetiology of this disease remains unclear, potential roles of infection, disordered cell biology, genetic influence etc. have been proposed. Pirfenidone and nintedanib are the only two US FDA approved drugs to treat pulmonary fibrosis. Autophagy is a catabolic intracellular pathway that plays a crucial role in maintaining cellular homeostasis, which is involved in many disorders including fibrotic diseases. The present study investigated the role of Nimbolide, an important active constituent of Neem in TGF-β1 induced in vitro and bleomycin induced in vivo model of pulmonary fibrosis, with a slight emphasis on regulation of fibrosis related autophagy. Protein expression studies showed significant reduction in mesenchymal, fibrotic markers and a substantial up regulation of epithelial markers upon treatment with Nimbolide. Nimbolide regulated autophagy signaling by dampening LC-3 and p-62 expression and increasing Beclin 1 expression as evidenced by immunohistochemistry and confocal microscopy. Our study demonstrates Nimbolide as a potent anti-fibrotic agent and its ability to regulate fibrosis associated autophagy.
|
Authors | M Prashanth Goud, Swarna Bale, Gauthami Pulivendala, Chandraiah Godugu |
Journal | International immunopharmacology
(Int Immunopharmacol)
Vol. 75
Pg. 105755
(Oct 2019)
ISSN: 1878-1705 [Electronic] Netherlands |
PMID | 31377591
(Publication Type: Journal Article)
|
Copyright | Copyright © 2019 Elsevier B.V. All rights reserved. |
Chemical References |
- Limonins
- Transforming Growth Factor beta1
- Bleomycin
- nimbolide
- Nitric Oxide
- L-Lactate Dehydrogenase
- Hydroxyproline
|
Topics |
- Animals
- Autophagy
(drug effects)
- Bleomycin
- Bronchoalveolar Lavage Fluid
(chemistry)
- Cell Line
- Cell Movement
(drug effects)
- Cell Survival
(drug effects)
- Epithelial-Mesenchymal Transition
(drug effects)
- Humans
- Hydroxyproline
(metabolism)
- L-Lactate Dehydrogenase
(metabolism)
- Limonins
(pharmacology, therapeutic use)
- Male
- Mice
- Nitric Oxide
(metabolism)
- Pulmonary Fibrosis
(chemically induced, drug therapy, pathology)
- Transforming Growth Factor beta1
|