FOLLOWUS
1. Pharmacy College, Jinan University,Guangzhou,China
2. State Key Laboratory of New-Tech for Chinese Medicine Pharmaceutical Process,Jiangsu Province,Lianyungang,China
纸质出版日期:2014,
网络出版日期:2014-6-10,
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Tang, Lp., Xiao, W., Li, Yf. et al. Anti-inflammatory effects of Reduning Injection (热毒宁注射液) on lipopolysaccharide-induced acute lung injury of rats., Chin. J. Integr. Med. 20, 591–599 (2014). https://doi.org/10.1007/s11655-014-1758-x
Lu-ping Tang, Wei Xiao, Yi-fang Li, et al. Anti-inflammatory effects of Reduning Injection (热毒宁注射液) on lipopolysaccharide-induced acute lung injury of rats[J]. Chinese Journal of Integrative Medicine, 2014,20(8):591-599.
Tang, Lp., Xiao, W., Li, Yf. et al. Anti-inflammatory effects of Reduning Injection (热毒宁注射液) on lipopolysaccharide-induced acute lung injury of rats., Chin. J. Integr. Med. 20, 591–599 (2014). https://doi.org/10.1007/s11655-014-1758-x DOI:
Lu-ping Tang, Wei Xiao, Yi-fang Li, et al. Anti-inflammatory effects of Reduning Injection (热毒宁注射液) on lipopolysaccharide-induced acute lung injury of rats[J]. Chinese Journal of Integrative Medicine, 2014,20(8):591-599. DOI: 10.1007/s11655-014-1758-x.
To evaluate the protective effects of Reduning Injection (热毒宁注射液
RDN)
a patent Chinese medicine
on lipopolysaccharide (LPS)-induced acute lung injury (ALI) in rats and its underlying mechanisms of action. Sixty male Sprague-Dawley rats were randomly divided into 6 groups
including normal control
model
dexamethasone (DEX
5 mg/kg)
RDN-H (720 mg/kg)
RDN-M (360 mg/kg) and RDN-L (180 mg/kg) groups
with 10 rats in each group. Rats were challenged with intravenous injection of LPS 1 h after intraperitoneal treatment with RDN or DEX. At 6 h after LPS challenge
lung tissues and bronchoalveolar lavage fluid (BALF) were collected
and the number of inflammatory cells was determined. The right lungs were collected for histopathologic examination
measurement of gene and protein expressions
superoxide dismutase (SOD) and myeloperoxidase (MPO) activities. In vivo pretreatment of RDN (360
720 mg/kg) significantly reduced the weight of wet to dry (W/D) ratio of lung
protein content in BALF
and led to remarkable attenuation of LPS-induced histopathological changes in the lungs. Meanwhile
RDN enormously decreased BALF total inflammatory cells
especially neutrophil and macrophage cell numbers. Moreover
RDN increased SOD activity
inhibited MPO activity
alleviated LPS-induced tumor neurosis factor-α (TNF-α) and inducible nitric oxide synthase (iNOS) expression in lung tissues. Furthermore
RDN (720 mg/kg) efficiently weakened nuclear factorkappa B (NF-κB) gene and protein expression. Anti-inflammatory effects of RDN was demonstrated to be preventing pulmonary neutrophil infiltration
lowering MPO activity
TNF-α and iNOS gene expression by inhibiting NF-κB activity in LPS-induced ALI.
To evaluate the protective effects of Reduning Injection (热毒宁注射液
RDN)
a patent Chinese medicine
on lipopolysaccharide (LPS)-induced acute lung injury (ALI) in rats and its underlying mechanisms of action. Sixty male Sprague-Dawley rats were randomly divided into 6 groups
including normal control
model
dexamethasone (DEX
5 mg/kg)
RDN-H (720 mg/kg)
RDN-M (360 mg/kg) and RDN-L (180 mg/kg) groups
with 10 rats in each group. Rats were challenged with intravenous injection of LPS 1 h after intraperitoneal treatment with RDN or DEX. At 6 h after LPS challenge
lung tissues and bronchoalveolar lavage fluid (BALF) were collected
and the number of inflammatory cells was determined. The right lungs were collected for histopathologic examination
measurement of gene and protein expressions
superoxide dismutase (SOD) and myeloperoxidase (MPO) activities. In vivo pretreatment of RDN (360
720 mg/kg) significantly reduced the weight of wet to dry (W/D) ratio of lung
protein content in BALF
and led to remarkable attenuation of LPS-induced histopathological changes in the lungs. Meanwhile
RDN enormously decreased BALF total inflammatory cells
especially neutrophil and macrophage cell numbers. Moreover
RDN increased SOD activity
inhibited MPO activity
alleviated LPS-induced tumor neurosis factor-α (TNF-α) and inducible nitric oxide synthase (iNOS) expression in lung tissues. Furthermore
RDN (720 mg/kg) efficiently weakened nuclear factorkappa B (NF-κB) gene and protein expression. Anti-inflammatory effects of RDN was demonstrated to be preventing pulmonary neutrophil infiltration
lowering MPO activity
TNF-α and iNOS gene expression by inhibiting NF-κB activity in LPS-induced ALI.
Acute Lung Injurylipopolysaccharideneutrophilschemokinenuclear factor-kappa BReduning InjectionChinese Patent Medicine
Acute Lung Injurylipopolysaccharideneutrophilschemokinenuclear factor-kappa BReduning InjectionChinese Patent Medicine
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