celecoxib has been researched along with Cirrhosis, Liver in 17 studies
Excerpt | Relevance | Reference |
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" This investigation consists of a double-blind, randomized, placebo-controlled trial aimed at comparing the effects of the selective COX-2 inhibitor celecoxib (200 mg every 12 hours for a total of 5 doses) on platelet and renal function and the renal response to furosemide (40 mg intravenously) with those of naproxen (500 mg every 12 hours for a total of 5 doses) and placebo in 28 patients with cirrhosis and ascites." | 9.11 | Effects of celecoxib and naproxen on renal function in nonazotemic patients with cirrhosis and ascites. ( Arroyo, V; Clària, J; Escolar, G; Ginès, P; Jiménez, W; Kent, JD; López-Parra, M; Ruiz-Del-Arbol, L; Vucelic, B, 2005) |
"Liver cirrhosis was induced by thioacetamide (TAA)." | 8.02 | Celecoxib ameliorates liver cirrhosis via reducing inflammation and oxidative stress along spleen-liver axis in rats. ( Gan, C; Gao, J; Huang, Z; Jia, X; Jiang, J; Liu, R; Ma, X; Su, W; Tai, Y; Tang, C; Tang, S; Wu, H; Ye, Y; Zhang, L; Zhao, C, 2021) |
"We evaluated the effects of concurrent use of methotrexate and celecoxib on silent liver and kidney damages in rheumatoid arthritis (RA) patients." | 7.80 | Concurrent use of methotrexate and celecoxib increases risk of silent liver fibrosis in rheumatoid arthritis patients with subclinical reduced kidney function. ( Lee, SK; Lee, SW; Park, JS; Park, MC; Park, YB, 2014) |
" We report in this study that a clinically available COX-2 inhibitor, celecoxib, exacerbates porcine serum (PS)-induced hepatic fibrosis and induces hepatocellular necrosis in an experimental liver fibrosis model." | 7.75 | Celecoxib exacerbates hepatic fibrosis and induces hepatocellular necrosis in rats treated with porcine serum. ( Li, X; Liu, H; Wei, W, 2009) |
" This investigation consists of a double-blind, randomized, placebo-controlled trial aimed at comparing the effects of the selective COX-2 inhibitor celecoxib (200 mg every 12 hours for a total of 5 doses) on platelet and renal function and the renal response to furosemide (40 mg intravenously) with those of naproxen (500 mg every 12 hours for a total of 5 doses) and placebo in 28 patients with cirrhosis and ascites." | 5.11 | Effects of celecoxib and naproxen on renal function in nonazotemic patients with cirrhosis and ascites. ( Arroyo, V; Clària, J; Escolar, G; Ginès, P; Jiménez, W; Kent, JD; López-Parra, M; Ruiz-Del-Arbol, L; Vucelic, B, 2005) |
"Liver cirrhosis was induced by thioacetamide (TAA)." | 4.02 | Celecoxib ameliorates liver cirrhosis via reducing inflammation and oxidative stress along spleen-liver axis in rats. ( Gan, C; Gao, J; Huang, Z; Jia, X; Jiang, J; Liu, R; Ma, X; Su, W; Tai, Y; Tang, C; Tang, S; Wu, H; Ye, Y; Zhang, L; Zhao, C, 2021) |
"We evaluated the effects of concurrent use of methotrexate and celecoxib on silent liver and kidney damages in rheumatoid arthritis (RA) patients." | 3.80 | Concurrent use of methotrexate and celecoxib increases risk of silent liver fibrosis in rheumatoid arthritis patients with subclinical reduced kidney function. ( Lee, SK; Lee, SW; Park, JS; Park, MC; Park, YB, 2014) |
" We report in this study that a clinically available COX-2 inhibitor, celecoxib, exacerbates porcine serum (PS)-induced hepatic fibrosis and induces hepatocellular necrosis in an experimental liver fibrosis model." | 3.75 | Celecoxib exacerbates hepatic fibrosis and induces hepatocellular necrosis in rats treated with porcine serum. ( Li, X; Liu, H; Wei, W, 2009) |
"B cells can promote liver fibrosis, but the mechanism of B cell infiltration and therapy against culprit B cells are lacking." | 1.91 | Disruption of cholangiocyte-B cell crosstalk by blocking the CXCL12-CXCR4 axis alleviates liver fibrosis. ( Dai, W; Gao, J; Huang, Z; Tang, C; Tong, H; Yang, W; Zhang, L; Zhao, C, 2023) |
"The animal models of liver fibrosis induced with TAA were established in rats and in intestinal epithelial-specific COX-2 knockout mice." | 1.62 | Inhibition of cyclooxygenase-2 enhanced intestinal epithelial homeostasis via suppressing β-catenin signalling pathway in experimental liver fibrosis. ( Gao, J; Ma, X; Tai, Y; Tang, C; Tang, S; Tong, H; Zhang, L; Zhao, C, 2021) |
"Celecoxib has been explored as a possible treatment of liver fibrosis with contradictory results, depending on the model." | 1.48 | Celecoxib Does Not Protect against Fibrosis and Inflammation in a Carbon Tetrachloride-Induced Model of Liver Injury. ( Hammock, BD; Harris, TR; Hwang, SH; Imai, DM; Kodani, S; Rand, AA; Yang, J, 2018) |
"As a result, liver fibrosis induced by TAA was significantly alleviated in the celecoxib group." | 1.43 | Inhibition of cyclooxygenase-2 alleviates liver cirrhosis via improvement of the dysfunctional gut-liver axis in rats. ( Gao, JH; Huang, ZY; Liu, R; Tai, Y; Tang, CW; Tang, SH; Tang, YM; Tong, H; Wang, CH; Wen, SL; Yan, ZP; Yang, JH; Yang, WJ; Ye, C, 2016) |
" Long-term administration of celecoxib, a selective cyclooxygenase-2 (COX-2) inhibitor, can ameliorate hepatic fibrosis." | 1.40 | Celecoxib attenuates hepatic cirrhosis through inhibition of epithelial-to-mesenchymal transition of hepatocytes. ( Gao, JH; Huang, ZY; Liu, ZX; Lu, YY; Tang, CW; Tong, H; Wen, SL; Yang, WJ, 2014) |
"Celecoxib treatment greatly reduced the tortuous hepatic portal venules." | 1.39 | Celecoxib ameliorates portal hypertension of the cirrhotic rats through the dual inhibitory effects on the intrahepatic fibrosis and angiogenesis. ( Gao, JH; Huang, ZY; Liu, ZX; Lu, YY; Tang, CW; Tong, H; Wen, SL; Yang, WJ, 2013) |
" The objective of this study was to evaluate the risk of upper GI adverse events associated with celecoxib and oral and parenteral non-selective NSAIDs in cirrhotic patients." | 1.38 | Non-steroidal anti-inflammatory drugs use and risk of upper gastrointestinal adverse events in cirrhotic patients. ( Chang, CH; Chen, HC; Lai, MS; Lee, YC; Lin, JW; Lin, MS, 2012) |
"Glycogen was decreased by CCl(4), while celecoxib partially prevented and reversed this effect." | 1.36 | Antifibrotic and fibrolytic properties of celecoxib in liver damage induced by carbon tetrachloride in the rat. ( Castro-Sánchez, L; Chávez, E; Moreno, MG; Muriel, P; Salazar, EP; Segovia, J; Shibayama, M; Tsutsumi, V; Vergara, P, 2010) |
"Celecoxib was used in the treatment of inflammation in patients with cirrhosis." | 1.35 | The anti-inflammatory effect of celecoxib does not prevent liver fibrosis in bile duct-ligated rats. ( Chan, HL; Cheung, KF; Chu, ES; Go, MY; Hui, AY; Sung, JJ; Wu, CW; Yu, J, 2009) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 5 (29.41) | 29.6817 |
2010's | 8 (47.06) | 24.3611 |
2020's | 4 (23.53) | 2.80 |
Authors | Studies |
---|---|
Zhang, L | 3 |
Zhao, C | 4 |
Dai, W | 1 |
Tong, H | 5 |
Yang, W | 1 |
Huang, Z | 2 |
Tang, C | 3 |
Gao, J | 3 |
Su, W | 2 |
Tai, Y | 4 |
Tang, SH | 2 |
Ye, YT | 1 |
Gao, JH | 4 |
Tuo, BG | 1 |
Tang, CW | 4 |
Tang, S | 2 |
Jiang, J | 1 |
Ma, X | 2 |
Ye, Y | 1 |
Gan, C | 1 |
Jia, X | 1 |
Liu, R | 2 |
Wu, H | 1 |
Chang, CC | 1 |
Lee, WS | 1 |
Hsieh, HG | 1 |
Chuang, CL | 1 |
Huang, HC | 1 |
Lee, FY | 1 |
Lee, SD | 1 |
Harris, TR | 1 |
Kodani, S | 1 |
Rand, AA | 1 |
Yang, J | 1 |
Imai, DM | 1 |
Hwang, SH | 1 |
Hammock, BD | 1 |
Wen, SL | 3 |
Yang, WJ | 3 |
Lu, YY | 2 |
Huang, ZY | 3 |
Liu, ZX | 2 |
Park, JS | 1 |
Park, MC | 1 |
Park, YB | 1 |
Lee, SK | 1 |
Lee, SW | 1 |
Wang, CH | 1 |
Yan, ZP | 1 |
Ye, C | 1 |
Tang, YM | 1 |
Yang, JH | 1 |
Liu, H | 1 |
Wei, W | 1 |
Li, X | 1 |
Chávez, E | 1 |
Segovia, J | 1 |
Shibayama, M | 1 |
Tsutsumi, V | 1 |
Vergara, P | 1 |
Castro-Sánchez, L | 1 |
Salazar, EP | 1 |
Moreno, MG | 1 |
Muriel, P | 1 |
Lee, YC | 1 |
Chang, CH | 1 |
Lin, JW | 1 |
Chen, HC | 1 |
Lin, MS | 1 |
Lai, MS | 1 |
Guevara, M | 1 |
Abecasis, R | 1 |
Terg, R | 1 |
Clària, J | 1 |
Kent, JD | 1 |
López-Parra, M | 1 |
Escolar, G | 1 |
Ruiz-Del-Arbol, L | 1 |
Ginès, P | 1 |
Jiménez, W | 1 |
Vucelic, B | 1 |
Arroyo, V | 1 |
Campbell, MS | 1 |
Makar, GA | 1 |
Yu, J | 1 |
Hui, AY | 1 |
Chu, ES | 1 |
Go, MY | 1 |
Cheung, KF | 1 |
Wu, CW | 1 |
Chan, HL | 1 |
Sung, JJ | 1 |
2 trials available for celecoxib and Cirrhosis, Liver
Article | Year |
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Effect of celecoxib on renal function in cirrhotic patients with ascites. A pilot study.
Topics: Adult; Aged; Celecoxib; Cyclooxygenase Inhibitors; Female; Humans; Kidney; Kidney Function Tests; Li | 2004 |
Effects of celecoxib and naproxen on renal function in nonazotemic patients with cirrhosis and ascites.
Topics: Ascites; Celecoxib; Dinoprostone; Double-Blind Method; Female; Furosemide; Glomerular Filtration Rat | 2005 |
15 other studies available for celecoxib and Cirrhosis, Liver
Article | Year |
---|---|
Disruption of cholangiocyte-B cell crosstalk by blocking the CXCL12-CXCR4 axis alleviates liver fibrosis.
Topics: Animals; Celecoxib; Cell Proliferation; Chemokine CXCL12; Cyclooxygenase 2; Epithelial Cells; Humans | 2023 |
Celecoxib attenuates hepatocyte apoptosis by inhibiting endoplasmic reticulum stress in thioacetamide-induced cirrhotic rats.
Topics: Animals; Apoptosis; Celecoxib; Endoplasmic Reticulum Stress; Endoribonucleases; Hepatocytes; Liver C | 2020 |
Celecoxib ameliorates liver cirrhosis via reducing inflammation and oxidative stress along spleen-liver axis in rats.
Topics: Animals; Apoptosis; Celecoxib; China; Cyclooxygenase 2 Inhibitors; Disease Models, Animal; Hepatic S | 2021 |
Inhibition of cyclooxygenase-2 enhanced intestinal epithelial homeostasis via suppressing β-catenin signalling pathway in experimental liver fibrosis.
Topics: Animals; beta Catenin; Celecoxib; Cell Line; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Disease | 2021 |
Selective cyclooxygenase inhibition by SC-560 improves hepatopulmonary syndrome in cirrhotic rats.
Topics: Animals; Celecoxib; Cyclooxygenase 1; Cyclooxygenase Inhibitors; Disease Models, Animal; Down-Regula | 2017 |
Celecoxib Does Not Protect against Fibrosis and Inflammation in a Carbon Tetrachloride-Induced Model of Liver Injury.
Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Carbon Tetrachloride; Celecoxib; Collagen; Cycloox | 2018 |
Celecoxib ameliorates portal hypertension of the cirrhotic rats through the dual inhibitory effects on the intrahepatic fibrosis and angiogenesis.
Topics: Angiogenesis Inhibitors; Animals; Celecoxib; Disease Models, Animal; Hypertension, Portal; Kidney; L | 2013 |
Celecoxib attenuates hepatic cirrhosis through inhibition of epithelial-to-mesenchymal transition of hepatocytes.
Topics: Animals; Celecoxib; Cyclooxygenase 2 Inhibitors; Disease Models, Animal; Down-Regulation; Epithelial | 2014 |
Concurrent use of methotrexate and celecoxib increases risk of silent liver fibrosis in rheumatoid arthritis patients with subclinical reduced kidney function.
Topics: Adult; Aged; Antirheumatic Agents; Arthritis, Rheumatoid; Celecoxib; Cross-Sectional Studies; Cycloo | 2014 |
Inhibition of cyclooxygenase-2 alleviates liver cirrhosis via improvement of the dysfunctional gut-liver axis in rats.
Topics: Animals; Caco-2 Cells; Cadherins; Celecoxib; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Dinopros | 2016 |
Celecoxib exacerbates hepatic fibrosis and induces hepatocellular necrosis in rats treated with porcine serum.
Topics: Animals; Body Weight; Celecoxib; Chemical and Drug Induced Liver Injury; Cyclooxygenase 2 Inhibitors | 2009 |
Antifibrotic and fibrolytic properties of celecoxib in liver damage induced by carbon tetrachloride in the rat.
Topics: Alanine Transaminase; Animals; Anti-Inflammatory Agents; Antioxidants; Aspartate Aminotransferases; | 2010 |
Non-steroidal anti-inflammatory drugs use and risk of upper gastrointestinal adverse events in cirrhotic patients.
Topics: Adult; Aged; Aged, 80 and over; Anti-Inflammatory Agents, Non-Steroidal; Celecoxib; Comorbidity; Cyc | 2012 |
Safety of short-term administration of celecoxib in decompensated cirrhosis.
Topics: Anti-Inflammatory Agents, Non-Steroidal; Celecoxib; Humans; Kidney Diseases; Liver Cirrhosis; Naprox | 2005 |
The anti-inflammatory effect of celecoxib does not prevent liver fibrosis in bile duct-ligated rats.
Topics: Alanine Transaminase; Animals; Anti-Inflammatory Agents, Non-Steroidal; Bile Ducts; Celecoxib; Inter | 2009 |