{"title":"The Inefficiency of Low-concentration Curcumin Intervention in Ameliorating\nChronic-stage Pulmonary Fibrosis","authors":"F. Muneesa M, Y. Bhandary","doi":"10.2174/1573407219666230810094839","DOIUrl":null,"url":null,"abstract":"\n\nCurcumin, a polyphenol compound, is reported to exhibit ameliorative\neffects in acute lung injury and different organ fibrosis models. We have previously demonstrated\nthat curcumin, at a dose of 75 mg/kg, could modulate inflammatory mediators and fibrinolytic system proteins in the inflammatory stage as well as fibroproliferative stage in a mouse model of bleomycin (BLM) induced pulmonary fibrosis. In this study, we investigated the efficacy of the same\ndose of curcumin in resolving the established fibrotic stage in a mouse model of BLM-induced\npulmonary fibrosis.\n\n\n\nWe prepared the fibrosis model by intranasal administration of BLM (2 mg/kg). Curcumin intervention was performed by intraperitoneal injection on 16th to 20th days post BLM exposure. The control group was administered with normal saline. The mice were sacrificed on the 21st\nday post BLM exposure.\n\n\n\nHistological analysis of the lung tissue samples indicated that curcumin (75 mg/kg) could\nnot reverse the fibrotic features induced by BLM. We also performed RT-PCR and western blot to\nexamine the molecular changes induced by BLM and curcumin. It was observed that curcumin\ncould neither reduce the expressions of fibrotic markers nor restore the normal expressions of proteins in the fibrinolytic system.\n\n\n\nOur data suggest that a low dose of curcumin is not effective in ameliorating the fibrotic stage of BLM-induced pulmonary fibrosis. An increased dose or a formulation that increases\nthe bioavailability of curcumin could probably exhibit promising effects against pulmonary fibrosis\nin the future.\n","PeriodicalId":10772,"journal":{"name":"Current Bioactive Compounds","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Bioactive Compounds","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1573407219666230810094839","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 0
Abstract
Curcumin, a polyphenol compound, is reported to exhibit ameliorative
effects in acute lung injury and different organ fibrosis models. We have previously demonstrated
that curcumin, at a dose of 75 mg/kg, could modulate inflammatory mediators and fibrinolytic system proteins in the inflammatory stage as well as fibroproliferative stage in a mouse model of bleomycin (BLM) induced pulmonary fibrosis. In this study, we investigated the efficacy of the same
dose of curcumin in resolving the established fibrotic stage in a mouse model of BLM-induced
pulmonary fibrosis.
We prepared the fibrosis model by intranasal administration of BLM (2 mg/kg). Curcumin intervention was performed by intraperitoneal injection on 16th to 20th days post BLM exposure. The control group was administered with normal saline. The mice were sacrificed on the 21st
day post BLM exposure.
Histological analysis of the lung tissue samples indicated that curcumin (75 mg/kg) could
not reverse the fibrotic features induced by BLM. We also performed RT-PCR and western blot to
examine the molecular changes induced by BLM and curcumin. It was observed that curcumin
could neither reduce the expressions of fibrotic markers nor restore the normal expressions of proteins in the fibrinolytic system.
Our data suggest that a low dose of curcumin is not effective in ameliorating the fibrotic stage of BLM-induced pulmonary fibrosis. An increased dose or a formulation that increases
the bioavailability of curcumin could probably exhibit promising effects against pulmonary fibrosis
in the future.
Current Bioactive CompoundsPharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.90
自引率
0.00%
发文量
112
期刊介绍:
The journal aims to provide comprehensive review articles on new bioactive compounds with proven activities in various biological screenings and pharmacological models with a special emphasis on stereoeselective synthesis. The aim is to provide a valuable information source of bioactive compounds synthesized or isolated, which can be used for further development of pharmaceuticals by industry and academia. The journal should prove to be essential reading for pharmacologists, natural product chemists and medicinal chemists who wish to be kept informed and up-to-date with the most important developments on new bioactive compounds of natural or synthetic origin, including their stereoeselective synthesis.