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Protective effects of Pudilan Tablets against osteoarthritis in mice induced by monosodium iodoacetate
by
Feng, Shibin
, Han, Rongchun
, Zhou, Chenyu
, Fang, Zhizheng
, Lei, Shujun
, Li, Xiangyu
, Tong, Xiaohui
in
631/154/436
/ 631/45/127/1213
/ 631/45/127/1220
/ AKT protein
/ Animal models
/ Animals
/ Anti-inflammatory agents
/ Anti-Inflammatory Agents - pharmacology
/ Arthritis
/ Cartilage diseases
/ Cartilage, Articular - metabolism
/ Cholecystokinin
/ Cytokines
/ Disease Models, Animal
/ Drugs, Chinese Herbal - pharmacology
/ Gene expression
/ Herbal medicine
/ Humanities and Social Sciences
/ IL-1β
/ Indomethacin
/ Inflammation
/ Interleukin 6
/ Interleukin-6 - metabolism
/ Iodoacetic Acid - toxicity
/ Joint diseases
/ Lipopolysaccharides
/ Mice
/ multidisciplinary
/ Osteoarthritis
/ Osteoarthritis - chemically induced
/ Osteoarthritis - drug therapy
/ Osteoarthritis - metabolism
/ RAW 264.7 Cells
/ Science
/ Science (multidisciplinary)
/ Signal transduction
/ Tablets
/ Traditional Chinese medicine
/ Tumor Necrosis Factor-alpha - metabolism
/ Tumor necrosis factor-α
2023
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Protective effects of Pudilan Tablets against osteoarthritis in mice induced by monosodium iodoacetate
by
Feng, Shibin
, Han, Rongchun
, Zhou, Chenyu
, Fang, Zhizheng
, Lei, Shujun
, Li, Xiangyu
, Tong, Xiaohui
in
631/154/436
/ 631/45/127/1213
/ 631/45/127/1220
/ AKT protein
/ Animal models
/ Animals
/ Anti-inflammatory agents
/ Anti-Inflammatory Agents - pharmacology
/ Arthritis
/ Cartilage diseases
/ Cartilage, Articular - metabolism
/ Cholecystokinin
/ Cytokines
/ Disease Models, Animal
/ Drugs, Chinese Herbal - pharmacology
/ Gene expression
/ Herbal medicine
/ Humanities and Social Sciences
/ IL-1β
/ Indomethacin
/ Inflammation
/ Interleukin 6
/ Interleukin-6 - metabolism
/ Iodoacetic Acid - toxicity
/ Joint diseases
/ Lipopolysaccharides
/ Mice
/ multidisciplinary
/ Osteoarthritis
/ Osteoarthritis - chemically induced
/ Osteoarthritis - drug therapy
/ Osteoarthritis - metabolism
/ RAW 264.7 Cells
/ Science
/ Science (multidisciplinary)
/ Signal transduction
/ Tablets
/ Traditional Chinese medicine
/ Tumor Necrosis Factor-alpha - metabolism
/ Tumor necrosis factor-α
2023
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Protective effects of Pudilan Tablets against osteoarthritis in mice induced by monosodium iodoacetate
by
Feng, Shibin
, Han, Rongchun
, Zhou, Chenyu
, Fang, Zhizheng
, Lei, Shujun
, Li, Xiangyu
, Tong, Xiaohui
in
631/154/436
/ 631/45/127/1213
/ 631/45/127/1220
/ AKT protein
/ Animal models
/ Animals
/ Anti-inflammatory agents
/ Anti-Inflammatory Agents - pharmacology
/ Arthritis
/ Cartilage diseases
/ Cartilage, Articular - metabolism
/ Cholecystokinin
/ Cytokines
/ Disease Models, Animal
/ Drugs, Chinese Herbal - pharmacology
/ Gene expression
/ Herbal medicine
/ Humanities and Social Sciences
/ IL-1β
/ Indomethacin
/ Inflammation
/ Interleukin 6
/ Interleukin-6 - metabolism
/ Iodoacetic Acid - toxicity
/ Joint diseases
/ Lipopolysaccharides
/ Mice
/ multidisciplinary
/ Osteoarthritis
/ Osteoarthritis - chemically induced
/ Osteoarthritis - drug therapy
/ Osteoarthritis - metabolism
/ RAW 264.7 Cells
/ Science
/ Science (multidisciplinary)
/ Signal transduction
/ Tablets
/ Traditional Chinese medicine
/ Tumor Necrosis Factor-alpha - metabolism
/ Tumor necrosis factor-α
2023
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Protective effects of Pudilan Tablets against osteoarthritis in mice induced by monosodium iodoacetate
Journal Article
Protective effects of Pudilan Tablets against osteoarthritis in mice induced by monosodium iodoacetate
2023
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Overview
Osteoarthritis (OA) is a complicated disorder that is the most prevalent chronic degenerative joint disease nowadays. Pudilan Tablets (PDL) is a prominent traditional Chinese medicine formula used in clinical settings to treat chronic inflammatory illnesses. However, there is currently minimal fundamental research on PDL in the therapy of joint diseases. As a result, this study looked at the anti-inflammatory and anti-OA properties of PDL in vitro and in vivo, as well as the mechanism of PDL in the treatment of OA. We investigated the anti-OA properties of PDL in OA mice that were generated by monosodium iodoacetate (MIA). All animals were administered PDL (2 g/kg or 4 g/kg) or the positive control drug, indomethacin (150 mg/kg), once daily for a total of 28 days starting on the day of MIA injection. The CCK-8 assay was used to test the vitality of PDL-treated RAW264.7 cells in vitro. RAW264.7 cells that had been activated with lipopolysaccharide (LPS) were used to assess the anti-inflammatory properties of PDL. In the MIA-induced OA model mice, PDL reduced pain, decreased OA-induced cartilage damages and degradation, decreased production of pro-inflammatory cytokines in serum, and suppressed
IL-1β
,
IL-6
, and
TNF-α
mRNA expression levels in tibiofemoral joint. In RAW264.7 cells, PDL treatment prevented LPS-induced activation of the ERK/Akt signaling pathway and significantly decreased the levels of inflammatory cytokines, such as IL-1β, IL-6, and TNF-α. In conclusion, these results suggest that PDL is involved in combating the development and progression of OA, exerts a powerful anti-inflammatory effect on the knee joint, and may be a promising candidate for the treatment of OA.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ Animals
/ Anti-Inflammatory Agents - pharmacology
/ Cartilage, Articular - metabolism
/ Drugs, Chinese Herbal - pharmacology
/ Humanities and Social Sciences
/ IL-1β
/ Mice
/ Osteoarthritis - chemically induced
/ Osteoarthritis - drug therapy
/ Science
/ Tablets
/ Traditional Chinese medicine
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