Page last updated: 2024-10-22

aristolochic acid i and Disease Models, Animal

aristolochic acid i has been researched along with Disease Models, Animal in 50 studies

aristolochic acid I: phospholipase A inhibitor
aristolochic acid A : An aristolochic acid that is phenanthrene-1-carboxylic acid that is substituted by a methylenedioxy group at the 3,4 positions, by a methoxy group at position 8, and by a nitro group at position 10. It is the most abundant of the aristolochic acids and is found in almost all Aristolochia (birthworts or pipevines) species. It has been tried in a number of treatments for inflammatory disorders, mainly in Chinese and folk medicine. However, there is concern over their use as aristolochic acid is both carcinogenic and nephrotoxic.

Disease Models, Animal: Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases.

Research Excerpts

ExcerptRelevanceReference
"This study was designed to investigate the roles of aristolochic acid I (AA-I) and hypokalemia in acute aristolochic acid nephropathy (AAN)."7.88Effects of aristolochic acid I and/or hypokalemia on tubular damage in C57BL/6 rat with aristolochic acid nephropathy. ( Han, SW; Kim, J; Kim, WY; Park, MH; Yi, JH, 2018)
"To investigate the therapeutic effects of endothelin receptor antagonist (bosentan) and angiotensin II type 1 receptor antagonist (valsartan) on renal interstitial fibrosis of rats with chronic aristolochic acid nephropathy (CAAN)."7.73[The therapeutic effects of bosentan and valsartan on renal interstitial fibrosis of chronic aristolochic acid nephropathy]. ( Chen, YP; Dong, HR; Qiu, CB; Zhang, C, 2005)
"Generally, renal aging is accompanied by renal fibrosis, which is the final common pathway of chronic kidney diseases."5.62Aristolochic Acid Induces Renal Fibrosis and Senescence in Mice. ( Abe, E; Atobe, Y; Azushima, K; Funakoshi, K; Kanaoka, T; Kinguchi, S; Suzuki, T; Taguchi, S; Tamura, K; Tanaka, S; Tsukamoto, S; Uneda, K; Urate, S; Wakui, H; Yamaji, T; Yamashita, A, 2021)
"Bortezomib (BZM) is a proteasome inhibitor used for the treatment of multiple myeloma (MM)."5.46The proteasome inhibitor bortezomib attenuates renal fibrosis in mice via the suppression of TGF-β1. ( Chiga, M; Isobe, K; Mandai, S; Mori, T; Nomura, N; Rai, T; Sohara, E; Uchida, S; Yui, N; Zeniya, M, 2017)
"Bardoxolone methyl (BARD) is an antioxidant modulator that acts through induction of the nuclear factor erythroid 2-related factor 2 (Nrf2) signaling pathway."5.40Bardoxolone methyl (BARD) ameliorates aristolochic acid (AA)-induced acute kidney injury through Nrf2 pathway. ( Chen, W; Fan, J; Feng, X; Liu, X; Wang, J; Wu, J; Yang, X; Yu, X; Zeng, Y, 2014)
" We used the Fucci mouse in conjunction with FlowSight to identify a discrete polyploid population in proximal tubules after aristolochic acid injury."3.91Novel kidney dissociation protocol and image-based flow cytometry facilitate improved analysis of injured proximal tubules. ( Alford, CE; Flaherty, DK; Gewin, LS; Ivanova, A; Lau, KS; Manolopoulou, M; Matlock, BK; Nlandu-Khodo, S; Phillips-Mignemi, M; Simmons, AJ, 2019)
"This study was designed to investigate the roles of aristolochic acid I (AA-I) and hypokalemia in acute aristolochic acid nephropathy (AAN)."3.88Effects of aristolochic acid I and/or hypokalemia on tubular damage in C57BL/6 rat with aristolochic acid nephropathy. ( Han, SW; Kim, J; Kim, WY; Park, MH; Yi, JH, 2018)
"To investigate the therapeutic effects of endothelin receptor antagonist (bosentan) and angiotensin II type 1 receptor antagonist (valsartan) on renal interstitial fibrosis of rats with chronic aristolochic acid nephropathy (CAAN)."3.73[The therapeutic effects of bosentan and valsartan on renal interstitial fibrosis of chronic aristolochic acid nephropathy]. ( Chen, YP; Dong, HR; Qiu, CB; Zhang, C, 2005)
"Generally, renal aging is accompanied by renal fibrosis, which is the final common pathway of chronic kidney diseases."1.62Aristolochic Acid Induces Renal Fibrosis and Senescence in Mice. ( Abe, E; Atobe, Y; Azushima, K; Funakoshi, K; Kanaoka, T; Kinguchi, S; Suzuki, T; Taguchi, S; Tamura, K; Tanaka, S; Tsukamoto, S; Uneda, K; Urate, S; Wakui, H; Yamaji, T; Yamashita, A, 2021)
"Renal fibrosis is a progressive pathological process that eventually leads to end-stage renal failure with limited therapeutic options."1.56Human umbilical cord mesenchymal stem cell attenuates renal fibrosis via TGF-β/Smad signaling pathways in vivo and in vitro. ( He, D; Hu, D; Lin, T; Liu, B; Liu, X; Long, C; Shen, L; Wei, G; Xiang, H; Xu, T; Yu, Y; Zhang, D; Zhang, Y; Zhou, Y, 2020)
"Bortezomib (BZM) is a proteasome inhibitor used for the treatment of multiple myeloma (MM)."1.46The proteasome inhibitor bortezomib attenuates renal fibrosis in mice via the suppression of TGF-β1. ( Chiga, M; Isobe, K; Mandai, S; Mori, T; Nomura, N; Rai, T; Sohara, E; Uchida, S; Yui, N; Zeniya, M, 2017)
"Bardoxolone methyl (BARD) is an antioxidant modulator that acts through induction of the nuclear factor erythroid 2-related factor 2 (Nrf2) signaling pathway."1.40Bardoxolone methyl (BARD) ameliorates aristolochic acid (AA)-induced acute kidney injury through Nrf2 pathway. ( Chen, W; Fan, J; Feng, X; Liu, X; Wang, J; Wu, J; Yang, X; Yu, X; Zeng, Y, 2014)
"Treatment with probenecid prevented increased plasma creatinine and tubulointerstitial injuries, and reduced both the extent and the severity of ultrastructural lesions induced by aristolochic acid, such as the loss of brush border, mitochondrial edema, and the disappearance of mitochondrial crests."1.38Probenecid prevents acute tubular necrosis in a mouse model of aristolochic acid nephropathy. ( Antoine, MH; Arlt, VM; Baudoux, TE; De Prez, EG; Goujon, JM; Nortier, JL; Pozdzik, AA; Quellard, N, 2012)
" In the present study, the effects of a chronic intake of AA given as a single drug was evaluated through renal histology and function in rabbits."1.31Chronic aristolochic acid toxicity in rabbits: a model of Chinese herbs nephropathy? ( Bernard, AM; Cosyns, JP; Dehoux, JP; Goebbels, RM; Guiot, Y; Robert, A; van Ypersele de Strihou, C, 2001)

Research

Studies (50)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (2.00)18.2507
2000's8 (16.00)29.6817
2010's27 (54.00)24.3611
2020's14 (28.00)2.80

Authors

AuthorsStudies
Abrams, RPM1
Yasgar, A1
Teramoto, T1
Lee, MH1
Dorjsuren, D1
Eastman, RT1
Malik, N1
Zakharov, AV1
Li, W1
Bachani, M1
Brimacombe, K1
Steiner, JP1
Hall, MD1
Balasubramanian, A1
Jadhav, A1
Padmanabhan, R1
Simeonov, A1
Nath, A1
Jiang, W1
Xu, C1
Xu, S1
Su, W1
Du, C1
Dong, J1
Feng, R1
Huang, C1
Li, J1
Ma, T1
Urate, S3
Wakui, H3
Azushima, K2
Yamaji, T3
Suzuki, T3
Abe, E3
Tanaka, S3
Taguchi, S2
Tsukamoto, S2
Kinguchi, S3
Uneda, K1
Kanaoka, T1
Atobe, Y1
Funakoshi, K1
Yamashita, A2
Tamura, K3
Kamimura, D1
Sasaki, K1
Terker, AS1
Tang, J1
Cao, S1
Arroyo, JP1
Niu, A1
Wang, S1
Fan, X1
Zhang, Y2
Bennett, SR1
Zhang, MZ1
Harris, RC2
Ren, J1
Rudemiller, NP1
Wen, Y1
Lu, X1
Privratsky, JR1
Crowley, SD1
Chen, SM4
Lin, CE2
Chen, HH1
Cheng, YF1
Cheng, HW1
Imai, K1
Chang, JF1
Hsieh, CY1
Lu, KC1
Chen, YW1
Liang, SS1
Lin, CC1
Hung, CF1
Liou, JC1
Wu, MS1
Yu, Y1
Hu, D1
Zhou, Y1
Xiang, H1
Liu, B1
Shen, L1
Long, C1
Liu, X3
Lin, T1
He, D1
Xu, T1
Zhang, D1
Wei, G1
Zhu, Z1
Xu, X2
Wang, F1
Song, Y2
Zhu, Y1
Quan, W1
Zhang, X3
Bi, C1
He, H1
Li, S1
Li, X1
Ishii, T1
Kumagae, T1
Kobayashi, R1
Haruhara, K1
Nakamura, T1
Kobayashi, S1
Lin, PY1
Yang, WC1
Huang, YS1
Lin, TY1
Chen, CM1
Chen, HS1
Lee, JA2
Lin, F1
Liu, Y1
Tang, L1
Chen, B2
Ren, Y1
Yang, X3
Li, L1
Tao, S1
Guo, F1
Liu, J1
Huang, R1
Tan, Z1
Zeng, X1
Ma, L1
Fu, P3
Succar, L1
Pianta, TJ1
Davidson, T1
Pickering, JW1
Endre, ZH1
Zeniya, M1
Mori, T1
Yui, N1
Nomura, N1
Mandai, S1
Isobe, K1
Chiga, M1
Sohara, E1
Rai, T1
Uchida, S1
Honarpisheh, M1
Foresto-Neto, O1
Steiger, S1
Kraft, F1
Koehler, P1
von Rauchhaupt, E1
Potempa, J1
Adamowicz, K1
Koziel, J1
Lech, M1
Shao, IH1
Chang, YH1
Pang, ST1
Manolopoulou, M1
Matlock, BK1
Nlandu-Khodo, S2
Simmons, AJ1
Lau, KS1
Phillips-Mignemi, M1
Ivanova, A1
Alford, CE1
Flaherty, DK1
Gewin, LS1
Donadei, C1
Angeletti, A1
Cantarelli, C1
D'Agati, VD1
La Manna, G1
Fiaccadori, E1
Horwitz, JK1
Xiong, H1
Guglielmo, C1
Hartzell, S1
Madsen, JC1
Maggiore, U1
Heeger, PS1
Cravedi, P1
Novitskaya, T1
McDermott, L1
Zhang, KX1
Chiba, T1
Paueksakon, P1
Hukriede, NA1
de Caestecker, MP1
Wu, J2
Fan, J2
Chen, W1
Wang, J2
Zeng, Y1
Feng, X2
Yu, X2
Neelisetty, S1
Alford, C1
Reynolds, K1
Woodbury, L1
Yang, H1
Fogo, AB1
Hao, CM1
Zent, R1
Gewin, L1
Samarakoon, R1
Helo, S1
Dobberfuhl, AD1
Khakoo, NS1
Falke, L1
Overstreet, JM1
Goldschmeding, R1
Higgins, PJ1
Dai, XY1
Zhou, L2
Huang, XR2
Lan, HY2
Zhao, YY2
Wang, HL1
Cheng, XL1
Wei, F1
Bai, X2
Lin, RC1
Vaziri, ND2
Lu, H1
Hong, W1
Liang, Y1
Bai, Y1
Chen, H1
Cao, G1
Chen, DQ1
Wang, M1
Zhang, ZH1
Mao, JR1
Yi, JH1
Han, SW1
Kim, WY1
Kim, J1
Park, MH1
Wen, YJ1
Qu, L1
Li, XM1
Liu, F1
Lai, KN1
Hamano, Y1
Aoki, T1
Shirai, R1
Hatano, M1
Kimura, R1
Ogawa, M2
Yokosuka, O1
Ueda, S2
Fragiadaki, M1
Witherden, AS1
Kaneko, T1
Sonnylal, S1
Pusey, CD1
Bou-Gharios, G1
Mason, RM1
Li, YC1
Tsai, SH1
Chang, YM1
Huang, TC1
Huang, YP1
Chang, CT1
Li, C1
Liang, A1
Gao, S1
Hui, L1
Liu, T1
Cao, C1
Zhao, Y1
Hao, R1
Yi, Y1
Guo, J1
Baudoux, TE1
Pozdzik, AA2
Arlt, VM3
De Prez, EG2
Antoine, MH1
Quellard, N1
Goujon, JM1
Nortier, JL3
Sabbisetti, VS1
Ito, K1
Wang, C1
Yang, L1
Mefferd, SC1
Bonventre, JV1
Debelle, F1
Nortier, J1
De Prez, E1
Vienne, A1
Salmon, I1
Phillips, DH2
Deschodt-Lanckman, M1
Vanherweghem, JL3
Lebeau, C1
Debelle, FD1
Pozdzik, A1
Deschodt-Lanckman, MM2
Zhang, C1
Chen, YP1
Dong, HR1
Qiu, CB1
Salmon, IJ1
Husson, CP1
Decaestecker, C1
Rogier, E1
Bourgeade, MF1
Lloret, S1
Moreno, JJ1
Cosyns, JP1
Dehoux, JP1
Guiot, Y1
Goebbels, RM1
Robert, A1
Bernard, AM1
van Ypersele de Strihou, C1
Zheng, F1
Huang, Q1
Chitme, HR1
Malipatil, M1
Chandrashekhar, VM1
Prashant, PM1
Li, M1
Ling, KH1
Lam, H1
Shaw, PC1
Cheng, L1
Techen, N1
Khan, LA1
Chang, YS1
But, PP1
Battu, GR1
Parimi, R1
Chandra Shekar, KB1
Kwak, DH1
Lee, JH1
Kim, T1
Ahn, HS1
Cho, WK1
Ha, H1
Hwang, YH1
Ma, JY1
Sato, N1
Takahashi, D1
Tsuchiya, R1
Mukoyama, T1
Yamagata, S1
Yoshida, M1
Kondo, S1
Satoh, N1

Reviews

1 review available for aristolochic acid i and Disease Models, Animal

ArticleYear
Recent advances in upper tract urothelial carcinomas: From bench to clinics.
    International journal of urology : official journal of the Japanese Urological Association, 2019, Volume: 26, Issue:2

    Topics: Animals; Antineoplastic Agents; Aristolochic Acids; Arsenic; Carcinogens; Carcinoma, Transitional Ce

2019

Other Studies

49 other studies available for aristolochic acid i and Disease Models, Animal

ArticleYear
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
    Proceedings of the National Academy of Sciences of the United States of America, 2020, 12-08, Volume: 117, Issue:49

    Topics: Animals; Antiviral Agents; Artificial Intelligence; Chlorocebus aethiops; Disease Models, Animal; Dr

2020
Macrophage-derived, LRG1-enriched extracellular vesicles exacerbate aristolochic acid nephropathy in a TGFβR1-dependent manner.
    Cell biology and toxicology, 2022, Volume: 38, Issue:4

    Topics: Animals; Aristolochic Acids; Disease Models, Animal; Extracellular Vesicles; Glycoproteins; Humans;

2022
Aristolochic Acid Induces Renal Fibrosis and Senescence in Mice.
    International journal of molecular sciences, 2021, Nov-18, Volume: 22, Issue:22

    Topics: Aging; Animals; Aristolochic Acids; beta-Galactosidase; Collagen; Cyclin-Dependent Kinase Inhibitor

2021
Effects of tumor necrosis factor-α inhibition on kidney fibrosis and inflammation in a mouse model of aristolochic acid nephropathy.
    Scientific reports, 2021, 12-08, Volume: 11, Issue:1

    Topics: Albuminuria; Animals; Aristolochic Acids; Collagen; Disease Models, Animal; Etanercept; Fibrosis; In

2021
Macrophage interferon regulatory factor 4 deletion ameliorates aristolochic acid nephropathy via reduced migration and increased apoptosis.
    JCI insight, 2022, 02-22, Volume: 7, Issue:4

    Topics: Animals; Apoptosis; Aristolochic Acids; Cells, Cultured; Disease Models, Animal; DNA; DNA Mutational

2022
The transcription factor Twist1 in the distal nephron but not in macrophages propagates aristolochic acid nephropathy.
    Kidney international, 2020, Volume: 97, Issue:1

    Topics: Animals; Apoptosis; Aristolochic Acids; Coculture Techniques; Disease Models, Animal; Epithelial Cel

2020
Effect of prednisolone on glyoxalase 1 in an inbred mouse model of aristolochic acid nephropathy using a proteomics method with fluorogenic derivatization-liquid chromatography-tandem mass spectrometry.
    PloS one, 2020, Volume: 15, Issue:1

    Topics: Animals; Aristolochic Acids; Chromatography, High Pressure Liquid; Disease Models, Animal; Female; F

2020
Therapeutic Targeting of Aristolochic Acid Induced Uremic Toxin Retention, SMAD 2/3 and JNK/ERK Pathways in Tubulointerstitial Fibrosis: Nephroprotective Role of Propolis in Chronic Kidney Disease.
    Toxins, 2020, 06-02, Volume: 12, Issue:6

    Topics: Animals; Aristolochic Acids; Cresols; Disease Models, Animal; Epithelial-Mesenchymal Transition; Ext

2020
Human umbilical cord mesenchymal stem cell attenuates renal fibrosis via TGF-β/Smad signaling pathways in vivo and in vitro.
    European journal of pharmacology, 2020, Sep-15, Volume: 883

    Topics: Animals; Aristolochic Acids; Cell Line; Coculture Techniques; Disease Models, Animal; Epithelial-Mes

2020
Integrative microRNA and mRNA expression profiling in acute aristolochic acid nephropathy in mice.
    Molecular medicine reports, 2020, Volume: 22, Issue:4

    Topics: Animals; Aristolochic Acids; Disease Models, Animal; Gene Expression Profiling; Gene Expression Regu

2020
Tissue xanthine oxidoreductase activity in a mouse model of aristolochic acid nephropathy.
    FEBS open bio, 2021, Volume: 11, Issue:2

    Topics: Animals; Aristolochic Acids; Disease Models, Animal; Fibrosis; Humans; Kidney Tubules; Male; Mice; R

2021
Evaluation of the nephrotoxicity and safety of low-dose aristolochic acid, extending to the use of Xixin (Asurum), by determination of methylglyoxal and d-lactate.
    Journal of ethnopharmacology, 2021, May-23, Volume: 272

    Topics: Animals; Aristolochic Acids; Collagen; Disease Models, Animal; Drugs, Chinese Herbal; Female; Fibros

2021
Rapamycin protects against aristolochic acid nephropathy in mice by potentiating mammalian target of rapamycin‑mediated autophagy.
    Molecular medicine reports, 2021, Volume: 24, Issue:1

    Topics: Animals; Apoptosis; Aristolochic Acids; Autophagy; Cell Line; Disease Models, Animal; Humans; Kidney

2021
Genetic and pharmacological inhibition of fatty acid-binding protein 4 alleviated inflammation and early fibrosis after toxin induced kidney injury.
    International immunopharmacology, 2021, Volume: 96

    Topics: Acute Kidney Injury; Animals; Aristolochic Acids; Biphenyl Compounds; Carcinogens; Disease Models, A

2021
Subclinical chronic kidney disease modifies the diagnosis of experimental acute kidney injury.
    Kidney international, 2017, Volume: 92, Issue:3

    Topics: Acute Kidney Injury; Adenine; Animals; Aristolochic Acids; Biomarkers; Cell Adhesion Molecules; Chem

2017
The proteasome inhibitor bortezomib attenuates renal fibrosis in mice via the suppression of TGF-β1.
    Scientific reports, 2017, 10-12, Volume: 7, Issue:1

    Topics: Animals; Aristolochic Acids; Bortezomib; Disease Models, Animal; Fibrosis; Kidney; Kidney Diseases;

2017
Aristolochic acid I determine the phenotype and activation of macrophages in acute and chronic kidney disease.
    Scientific reports, 2018, 08-15, Volume: 8, Issue:1

    Topics: Acute Kidney Injury; Animals; Aristolochic Acids; Cisplatin; Disease Models, Animal; Female; Fibrosi

2018
Novel kidney dissociation protocol and image-based flow cytometry facilitate improved analysis of injured proximal tubules.
    American journal of physiology. Renal physiology, 2019, 05-01, Volume: 316, Issue:5

    Topics: Acute Kidney Injury; Animals; Aristolochic Acids; Biomarkers; Cell Cycle; Cell Separation; Disease M

2019
Erythropoietin inhibits SGK1-dependent TH17 induction and TH17-dependent kidney disease.
    JCI insight, 2019, 04-23, Volume: 5

    Topics: Animals; Aristolochic Acids; Cells, Cultured; Disease Models, Animal; Epoetin Alfa; Erythropoietin;

2019
A PTBA small molecule enhances recovery and reduces postinjury fibrosis after aristolochic acid-induced kidney injury.
    American journal of physiology. Renal physiology, 2014, Mar-01, Volume: 306, Issue:5

    Topics: Acute Kidney Injury; Animals; Aristolochic Acids; Butyrates; Disease Models, Animal; Fibrosis; Histo

2014
Bardoxolone methyl (BARD) ameliorates aristolochic acid (AA)-induced acute kidney injury through Nrf2 pathway.
    Toxicology, 2014, Apr-06, Volume: 318

    Topics: Acute Kidney Injury; Animals; Aristolochic Acids; Cryoprotective Agents; Disease Models, Animal; Hem

2014
Renal fibrosis is not reduced by blocking transforming growth factor-β signaling in matrix-producing interstitial cells.
    Kidney international, 2015, Volume: 88, Issue:3

    Topics: Actins; Animals; Aristolochic Acids; Cells, Cultured; Collagen Type I; Disease Models, Animal; Extra

2015
Loss of tumour suppressor PTEN expression in renal injury initiates SMAD3- and p53-dependent fibrotic responses.
    The Journal of pathology, 2015, Volume: 236, Issue:4

    Topics: Animals; Apoptosis; Aristolochic Acids; Cell Cycle Checkpoints; Cell Line; Cell Proliferation; Disea

2015
Smad7 protects against chronic aristolochic acid nephropathy in mice.
    Oncotarget, 2015, May-20, Volume: 6, Issue:14

    Topics: Animals; Aristolochic Acids; Blotting, Western; Disease Models, Animal; Drugs, Chinese Herbal; Gene

2015
Metabolomics analysis reveals the association between lipid abnormalities and oxidative stress, inflammation, fibrosis, and Nrf2 dysfunction in aristolochic acid-induced nephropathy.
    Scientific reports, 2015, Aug-07, Volume: 5

    Topics: Animals; Aristolochic Acids; Disease Models, Animal; Fibrosis; Inflammation; Kidney; Lipids; Male; M

2015
Possible role of mitochondrial injury in Caulis Aristolochia manshuriensis-induced chronic aristolochic acid nephropathy.
    Drug and chemical toxicology, 2017, Volume: 40, Issue:1

    Topics: Animals; Apoptosis; Aristolochia; Aristolochic Acids; Biomarkers; Disease Models, Animal; Dose-Respo

2017
Transforming growth factor-β1 stimulates hedgehog signaling to promote epithelial-mesenchymal transition after kidney injury.
    The FEBS journal, 2016, Volume: 283, Issue:20

    Topics: Animals; Aristolochic Acids; Cell Line; Disease Models, Animal; Disease Progression; Epithelial-Mese

2016
Metabolomics insights into activated redox signaling and lipid metabolism dysfunction in chronic kidney disease progression.
    Redox biology, 2016, Volume: 10

    Topics: Adenine; Animals; Aristolochic Acids; Biomarkers; Disease Models, Animal; Disease Progression; Early

2016
Effects of aristolochic acid I and/or hypokalemia on tubular damage in C57BL/6 rat with aristolochic acid nephropathy.
    The Korean journal of internal medicine, 2018, Volume: 33, Issue:4

    Topics: Animals; Aristolochic Acids; Disease Models, Animal; Hypokalemia; Kidney Diseases; Kidney Tubules; M

2018
Ischemic injury underlies the pathogenesis of aristolochic acid-induced acute kidney injury.
    Translational research : the journal of laboratory and clinical medicine, 2008, Volume: 152, Issue:1

    Topics: Acute Disease; Animals; Aristolochia; Aristolochic Acids; Blotting, Western; Cell Nucleus; Creatinin

2008
Activation of p53 promotes renal injury in acute aristolochic acid nephropathy.
    Journal of the American Society of Nephrology : JASN, 2010, Volume: 21, Issue:1

    Topics: Animals; Apoptosis; Aristolochic Acids; Benzothiazoles; Cells, Cultured; Disease Models, Animal; Dos

2010
Low-dose darbepoetin alpha attenuates progression of a mouse model of aristolochic acid nephropathy through early tubular protection.
    Nephron. Experimental nephrology, 2010, Volume: 114, Issue:2

    Topics: Animals; Apoptosis; Aristolochic Acids; Cell Proliferation; Darbepoetin alfa; Disease Models, Animal

2010
Interstitial fibrosis is associated with increased COL1A2 transcription in AA-injured renal tubular epithelial cells in vivo.
    Matrix biology : journal of the International Society for Matrix Biology, 2011, Volume: 30, Issue:7-8

    Topics: Animals; Aristolochic Acids; Biomarkers; Blood Urea Nitrogen; Cadherins; Collagen Type I; Connective

2011
Aristolochic acid-induced accumulation of methylglyoxal and Nε-(carboxymethyl)lysine: an important and novel pathway in the pathogenic mechanism for aristolochic acid nephropathy.
    Biochemical and biophysical research communications, 2012, Jul-13, Volume: 423, Issue:4

    Topics: Animals; Aristolochic Acids; Creatine; Disease Models, Animal; Female; Kidney; Lysine; Mice; Mice, I

2012
[Development of gastric precancerous lesion animal model].
    Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 2012, Volume: 37, Issue:1

    Topics: Animals; Aristolochia; Aristolochic Acids; Disease Models, Animal; Drugs, Chinese Herbal; Humans; Ma

2012
Probenecid prevents acute tubular necrosis in a mouse model of aristolochic acid nephropathy.
    Kidney international, 2012, Volume: 82, Issue:10

    Topics: Animals; Aristolochic Acids; Atrophy; Biomarkers; Cell Proliferation; Cell Survival; Creatinine; Cyt

2012
Novel assays for detection of urinary KIM-1 in mouse models of kidney injury.
    Toxicological sciences : an official journal of the Society of Toxicology, 2013, Volume: 131, Issue:1

    Topics: Animals; Aristolochic Acids; Biological Assay; Biomarkers; Disease Models, Animal; Hepatitis A Virus

2013
Effects of dexfenfluramine on aristolochic acid nephrotoxicity in a rat model for Chinese-herb nephropathy.
    Archives of toxicology, 2003, Volume: 77, Issue:4

    Topics: Animals; Aristolochic Acids; Autoradiography; Body Weight; Creatinine; Dexfenfluramine; Disease Mode

2003
Early proximal tubule injury in experimental aristolochic acid nephropathy: functional and histological studies.
    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2005, Volume: 20, Issue:11

    Topics: Acetylglucosaminidase; Albumins; Animals; Aristolochic Acids; Biomarkers; Carcinogens; Chromatograph

2005
[The therapeutic effects of bosentan and valsartan on renal interstitial fibrosis of chronic aristolochic acid nephropathy].
    Zhonghua yi xue za zhi, 2005, Sep-28, Volume: 85, Issue:37

    Topics: Animals; Aristolochic Acids; Bosentan; Collagen Type I; Connective Tissue Growth Factor; Disease Mod

2005
Patterns of interstitial inflammation during the evolution of renal injury in experimental aristolochic acid nephropathy.
    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2008, Volume: 23, Issue:8

    Topics: Animals; Aristolochic Acids; Disease Models, Animal; Fibrosis; Kidney; Kidney Failure, Chronic; Macr

2008
Effect of nonapeptide fragments of uteroglobin and lipocortin I on oedema and mast cell degranulation.
    European journal of pharmacology, 1994, Nov-03, Volume: 264, Issue:3

    Topics: Animals; Annexin A1; Aristolochic Acids; Carrageenan; Cell Degranulation; Chlorpheniramine; Dexameth

1994
Chronic aristolochic acid toxicity in rabbits: a model of Chinese herbs nephropathy?
    Kidney international, 2001, Volume: 59, Issue:6

    Topics: Animals; Aristolochic Acids; Disease Models, Animal; Drugs, Chinese Herbal; Enzyme Inhibitors; Femal

2001
[Establishment of model of aristolochic acid-induced chronic renal interstitial fibrosis in rats].
    Zhonghua yi xue za zhi, 2001, Sep-25, Volume: 81, Issue:18

    Topics: Animals; Aristolochic Acids; Blood Urea Nitrogen; Body Weight; Carcinogens; Chronic Disease; Creatin

2001
Antiallergic activity of Aristolochia bracteolata Lank in animal model.
    Indian journal of experimental biology, 2010, Volume: 48, Issue:1

    Topics: Anaphylaxis; Animals; Anti-Allergic Agents; Aristolochia; Dermatitis; Disease Models, Animal; Female

2010
Cardiocrinum seeds as a replacement for Aristolochia fruits in treating cough.
    Journal of ethnopharmacology, 2010, Jul-20, Volume: 130, Issue:2

    Topics: Animals; Antitussive Agents; Aristolochia; Base Sequence; Citric Acid; Cough; Disease Models, Animal

2010
In vivo and in vitro pharmacological activity of Aristolochia tagala (syn: Aristolochia acuminata) root extracts.
    Pharmaceutical biology, 2011, Volume: 49, Issue:11

    Topics: Acetates; Alkanes; Animals; Anti-Inflammatory Agents; Aristolochia; Calcimycin; Calcium Ionophores;

2011
Aristolochia manshuriensis Kom inhibits adipocyte differentiation by regulation of ERK1/2 and Akt pathway.
    PloS one, 2012, Volume: 7, Issue:11

    Topics: 3T3-L1 Cells; Adipocytes; Adipogenesis; Animals; Aristolochia; Cell Differentiation; Cell Survival;

2012
Acute nephrotoxicity of aristolochic acids in mice.
    The Journal of pharmacy and pharmacology, 2004, Volume: 56, Issue:2

    Topics: Acute Disease; Administration, Oral; Animals; Aristolochia; Aristolochic Acids; Blood Urea Nitrogen;

2004