Paricalcitol (BioDeep_00000638152)

Main id: BioDeep_00000006667

 


代谢物信息卡片


(1R,3R,7E)-17beta-[(2R,3E,5S)-6-hydroxy-5,6-dimethylhept-3-en-2-yl]-9,10-secoestra-5,7-diene-1,3-diol

化学式: C27H44O3 (416.329)
中文名称: 帕立骨化醇
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1CC/C(=C\C=C2\C[C@H](C[C@H](O)C\2)O)/[C@]2([H])CC[C@]([H])([C@@H](/C=C/[C@H](C)C(O)(C)C)C)[C@]21C
InChI: InChI=1S/C27H44O3/c1-18(8-9-19(2)26(3,4)30)24-12-13-25-21(7-6-14-27(24,25)5)11-10-20-15-22(28)17-23(29)16-20/h8-11,18-19,22-25,28-30H,6-7,12-17H2,1-5H3/b9-8+,21-11+/t18-,19+,22-,23-,24-,25+,27-/m1/s1

描述信息

H - Systemic hormonal preparations, excl. sex hormones and insulins > H05 - Calcium homeostasis > H05B - Anti-parathyroid agents
D018977 - Micronutrients > D014815 - Vitamins > D004872 - Ergocalciferols

同义名列表

5 个代谢物同义名

Paricalcitol; (1R,3R,7E)-17beta-[(2R,3E,5S)-6-hydroxy-5,6-dimethylhept-3-en-2-yl]-9,10-secoestra-5,7-diene-1,3-diol; 19-Nor-1alpha,25-dihydroxyvitamin D2; ST 27:2;O3; Paricalcitol



数据库引用编号

12 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

0 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 10 ACE, ALB, APOE, BGLAP, CASP3, CTNNB1, EGFR, FGF23, VDR, VEGFA
Peripheral membrane protein 1 GORASP1
Endosome membrane 1 EGFR
Endoplasmic reticulum membrane 1 EGFR
Nucleus 7 ALB, APOE, CASP3, CTNNB1, EGFR, VDR, VEGFA
cytosol 4 ALB, CASP3, CTNNB1, VDR
dendrite 2 APOE, BGLAP
centrosome 2 ALB, CTNNB1
nucleoplasm 3 CASP3, CTNNB1, VDR
RNA polymerase II transcription regulator complex 1 VDR
Cell membrane 4 ACE, CTNNB1, EGFR, TNF
Cytoplasmic side 1 GORASP1
lamellipodium 1 CTNNB1
ruffle membrane 1 EGFR
Early endosome membrane 1 EGFR
Golgi apparatus membrane 1 GORASP1
Synapse 1 CTNNB1
cell cortex 1 CTNNB1
cell junction 2 CTNNB1, EGFR
cell surface 3 EGFR, TNF, VEGFA
glutamatergic synapse 4 APOE, CASP3, CTNNB1, EGFR
Golgi apparatus 4 ALB, APOE, GORASP1, VEGFA
Golgi membrane 3 EGFR, GORASP1, INS
neuronal cell body 3 APOE, CASP3, TNF
presynaptic membrane 1 CTNNB1
Lysosome 1 ACE
endosome 2 ACE, EGFR
plasma membrane 7 ACE, APOE, CTNNB1, EGFR, KL, REN, TNF
Membrane 7 ACE, APOE, CTNNB1, EGFR, KL, REN, VEGFA
apical plasma membrane 2 EGFR, KL
basolateral plasma membrane 2 CTNNB1, EGFR
extracellular exosome 5 ACE, ALB, APOE, CTNNB1, KL
endoplasmic reticulum 3 ALB, APOE, VEGFA
extracellular space 16 ACE, ALB, APOE, BGLAP, CCL2, CRP, EGFR, FGF23, IL10, IL6, INS, KL, PTH, REN, TNF, VEGFA
perinuclear region of cytoplasm 2 CTNNB1, EGFR
Schaffer collateral - CA1 synapse 1 CTNNB1
adherens junction 2 CTNNB1, VEGFA
apicolateral plasma membrane 1 CTNNB1
bicellular tight junction 1 CTNNB1
protein-containing complex 3 ALB, CTNNB1, EGFR
postsynaptic density 1 CASP3
Single-pass type I membrane protein 3 ACE, EGFR, KL
Secreted 12 ACE, ALB, APOE, BGLAP, CCL2, CRP, FGF23, IL10, IL6, INS, REN, VEGFA
extracellular region 15 ACE, ALB, APOE, BGLAP, CCL2, CRP, FGF23, IL10, IL6, INS, KL, PTH, REN, TNF, VEGFA
[Isoform 2]: Secreted 1 KL
anchoring junction 1 ALB
transcription regulator complex 1 CTNNB1
nuclear membrane 1 EGFR
external side of plasma membrane 2 ACE, TNF
Endosome, multivesicular body 1 APOE
Extracellular vesicle 1 APOE
Secreted, extracellular space, extracellular matrix 2 APOE, VEGFA
chylomicron 1 APOE
high-density lipoprotein particle 1 APOE
low-density lipoprotein particle 1 APOE
multivesicular body 1 APOE
very-low-density lipoprotein particle 1 APOE
perikaryon 1 BGLAP
Z disc 1 CTNNB1
beta-catenin destruction complex 1 CTNNB1
Wnt signalosome 1 CTNNB1
Early endosome 1 APOE
apical part of cell 2 CTNNB1, REN
cell-cell junction 1 CTNNB1
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
vesicle 1 BGLAP
postsynaptic membrane 1 CTNNB1
Apical cell membrane 1 KL
Membrane raft 2 EGFR, TNF
Cytoplasm, cytoskeleton 1 CTNNB1
focal adhesion 2 CTNNB1, EGFR
cis-Golgi network 1 GORASP1
Cell junction, adherens junction 1 CTNNB1
flotillin complex 1 CTNNB1
extracellular matrix 2 APOE, VEGFA
intracellular vesicle 1 EGFR
collagen-containing extracellular matrix 1 APOE
secretory granule 1 VEGFA
fascia adherens 1 CTNNB1
lateral plasma membrane 1 CTNNB1
receptor complex 2 EGFR, VDR
ciliary basal body 1 ALB
chromatin 1 VDR
phagocytic cup 1 TNF
cell periphery 1 CTNNB1
Cytoplasm, cytoskeleton, cilium basal body 1 CTNNB1
centriole 1 ALB
Secreted, extracellular space 1 APOE
brush border membrane 1 ACE
spindle pole 2 ALB, CTNNB1
blood microparticle 2 ALB, APOE
sperm midpiece 1 ACE
postsynaptic density, intracellular component 1 CTNNB1
microvillus membrane 1 CTNNB1
Endomembrane system 1 CTNNB1
endosome lumen 1 INS
Melanosome 1 APOE
euchromatin 1 CTNNB1
basal plasma membrane 2 ACE, EGFR
synaptic membrane 1 EGFR
secretory granule lumen 1 INS
Golgi lumen 3 BGLAP, FGF23, INS
endoplasmic reticulum lumen 6 ALB, APOE, BGLAP, FGF23, IL6, INS
platelet alpha granule lumen 2 ALB, VEGFA
transport vesicle 1 INS
beta-catenin-TCF complex 1 CTNNB1
Endoplasmic reticulum-Golgi intermediate compartment membrane 2 GORASP1, INS
Golgi apparatus, cis-Golgi network membrane 1 GORASP1
presynaptic active zone cytoplasmic component 1 CTNNB1
clathrin-coated endocytic vesicle membrane 2 APOE, EGFR
synaptic cleft 1 APOE
protein-DNA complex 1 CTNNB1
death-inducing signaling complex 1 CASP3
[Isoform 1]: Cell membrane 1 KL
catenin complex 1 CTNNB1
discoidal high-density lipoprotein particle 1 APOE
multivesicular body, internal vesicle lumen 1 EGFR
Shc-EGFR complex 1 EGFR
endocytic vesicle lumen 1 APOE
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
chylomicron remnant 1 APOE
intermediate-density lipoprotein particle 1 APOE
lipoprotein particle 1 APOE
multivesicular body, internal vesicle 1 APOE
interleukin-6 receptor complex 1 IL6
[Angiotensin-converting enzyme, soluble form]: Secreted 1 ACE
[Isoform Testis-specific]: Cell membrane 1 ACE
[N-VEGF]: Cytoplasm 1 VEGFA
[VEGFA]: Secreted 1 VEGFA
[Isoform L-VEGF189]: Endoplasmic reticulum 1 VEGFA
[Isoform VEGF121]: Secreted 1 VEGFA
[Isoform VEGF165]: Secreted 1 VEGFA
VEGF-A complex 1 VEGFA
beta-catenin-TCF7L2 complex 1 CTNNB1
beta-catenin-ICAT complex 1 CTNNB1
Scrib-APC-beta-catenin complex 1 CTNNB1
ciliary transition fiber 1 ALB
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF
[Klotho peptide]: Secreted 1 KL


文献列表

  • Abdulrahman Mujalli, Wesam F Farrash, Ahmad A Obaid, Anmar A Khan, Riyad A Almaimani, Shakir Idris, Mohamed E Elzubier, Elshiekh Babiker A Khidir, Akhmed Aslam, Faisal Minshawi, Mohammad A Alobaidy, Adel B Alharbi, Hussain A Almasmoum, Mazen Ghaith, Khalid Alqethami, Bassem Refaat. Improved Glycaemic Control and Nephroprotective Effects of Empagliflozin and Paricalcitol Co-Therapy in Mice with Type 2 Diabetes Mellitus. International journal of molecular sciences. 2023 Dec; 24(24):. doi: 10.3390/ijms242417380. [PMID: 38139208]
  • Mohamed El-Boshy, Aiman Alsaegh, Ahmed H Qasem, Ramya A Sindi, Abdelghany H Abdelghany, Hossam Gadalla, Doha Reda, Firas Azzeh, Shakir Idris, Jawwad Ahmad, Bassem Refaat. Enhanced renoprotective actions of Paricalcitol and omega-3 fatty acids co-therapy against diabetic nephropathy in rat. Journal of advanced research. 2022 05; 38(?):119-129. doi: 10.1016/j.jare.2021.08.010. [PMID: 35572411]
  • Hina L Nizami, Parmeshwar B Katare, Pankaj Prabhakar, Ramu Adela, Soumalya Sarkar, Sudheer Arava, Praloy Chakraborty, Subir K Maulik, Sanjay K Banerjee. Paricalcitol Attenuates Metabolic Syndrome-Associated Heart Failure through Enhanced Mitochondrial Fusion. Oxidative medicine and cellular longevity. 2022; 2022(?):5554290. doi: 10.1155/2022/5554290. [PMID: 35726330]
  • Niansong Wang, Yuting Xie, Gengru Jiang. Efficacy and safety of intravenous paricalcitol treatment in Chinese hemodialysis patients: a real-world database analysis. Annals of palliative medicine. 2022 Jan; 11(1):225-239. doi: 10.21037/apm-21-3966. [PMID: 35144414]
  • Farhad Koohpeyma, Gholamhossein Ranjbar Omrani, Ali Zamani, Forough Saki. Effects of Paricalcitol on Body Composition in Vitamin D-Deficient Rats. Iranian journal of medical sciences. 2021 11; 46(6):468-474. doi: 10.30476/ijms.2020.85368.1503. [PMID: 34840387]
  • Jing Huang, Qi An, Bo-Miao Ju, Jing Zhang, Ping Fan, Lan He, Lei Wang. Role of vitamin D/VDR nuclear translocation in down-regulation of NF-κB/NLRP3/caspase-1 axis in lupus nephritis. International immunopharmacology. 2021 Nov; 100(?):108131. doi: 10.1016/j.intimp.2021.108131. [PMID: 34536747]
  • Bin Wang, Jing-Yi Qian, Tao-Tao Tang, Li-Lu Lin, Nan Yu, Hong-Lei Guo, Wei-Jie Ni, Ling-Li Lv, Yi Wen, Zuo-Lin Li, Min Wu, Jing-Yuan Cao, Bi-Cheng Liu. VDR/Atg3 Axis Regulates Slit Diaphragm to Tight Junction Transition via p62-Mediated Autophagy Pathway in Diabetic Nephropathy. Diabetes. 2021 11; 70(11):2639-2651. doi: 10.2337/db21-0205. [PMID: 34376476]
  • Raquel Martínez-Pulleiro, María García-Murias, Manuel Fidalgo-Díaz, Miguel Ángel García-González. Molecular Basis, Diagnostic Challenges and Therapeutic Approaches of Alport Syndrome: A Primer for Clinicians. International journal of molecular sciences. 2021 Oct; 22(20):. doi: 10.3390/ijms222011063. [PMID: 34681722]
  • Yue Qu, Yuche Wu, Hong Jiang. Research progress in the pharmacological actions of the multiple effects and selectivity of the vitamin D analogue paricalcitol: a narrative review. Annals of palliative medicine. 2021 10; 10(10):11177-11190. doi: 10.21037/apm-21-2249. [PMID: 34763476]
  • Jeong-Hoon Lim, Ju-Min Yook, Se-Hyun Oh, Soo-Jee Jeon, Hee Won Noh, Hee-Yeon Jung, Ji-Young Choi, Jang-Hee Cho, Chan-Duck Kim, Yong-Lim Kim, Sun-Hee Park. Paricalcitol Improves Hypoxia-Induced and TGF-β1-Induced Injury in Kidney Pericytes. International journal of molecular sciences. 2021 Sep; 22(18):. doi: 10.3390/ijms22189751. [PMID: 34575914]
  • María Dolores Arenas Jimenez, Emilio González-Parra, Marta Riera, Abraham Rincón Bello, Ana López-Herradón, Higini Cao, Sara Hurtado, Silvia Collado, Laura Ribera, Francesc Barbosa, Fabiola Dapena, Vicent Torregrosa, José-Jesús Broseta, Carlos Soto Montañez, Juan F Navarro-González, Rosa Ramos, Jordi Bover, Xavier Nogués-Solan, Marta Crespo, Adriana S Dusso, Julio Pascual. Mortality in Hemodialysis Patients with COVID-19, the Effect of Paricalcitol or Calcimimetics. Nutrients. 2021 Jul; 13(8):. doi: 10.3390/nu13082559. [PMID: 34444716]
  • Hasan Haci Yeter, Berfu Korucu, Elif Burcu Bali, Ulver Derici. Association between calcitriol and paricalcitol with oxidative stress in patients with hemodialysis. International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition. 2021 Jun; 91(3-4):335-342. doi: 10.1024/0300-9831/a000641. [PMID: 32065560]
  • Laura Martínez-Arias, Sara Panizo, Cristina Alonso-Montes, Julia Martín-Vírgala, Beatriz Martín-Carro, Sara Fernández-Villabrille, Carmen García Gil-Albert, Carmen Palomo-Antequera, José Luis Fernández-Martín, María Piedad Ruiz-Torres, Adriana S Dusso, Natalia Carrillo-López, Jorge B Cannata-Andía, Manuel Naves-Díaz. Effects of calcitriol and paricalcitol on renal fibrosis in CKD. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 2021 04; 36(5):793-803. doi: 10.1093/ndt/gfaa373. [PMID: 33416889]
  • Fadime Demir, Mustafa Demir, Hatice Aygun. Evaluation of the protective effect of paricalcitol and vitamin D3 at doxorubicin nephrotoxicity in rats with 99mTechnetium-dimercaptosuccinic acid renal scintigraphy and biochemical methods. Human & experimental toxicology. 2021 Feb; 40(2):274-283. doi: 10.1177/0960327120950010. [PMID: 32812453]
  • Siqing Jiang, Hao Zhang, Xin Li, Bin Yi, Lihua Huang, Zhaoxin Hu, Aimei Li, Jie Du, Yanchun Li, Wei Zhang. Vitamin D/VDR attenuate cisplatin-induced AKI by down-regulating NLRP3/Caspase-1/GSDMD pyroptosis pathway. The Journal of steroid biochemistry and molecular biology. 2021 02; 206(?):105789. doi: 10.1016/j.jsbmb.2020.105789. [PMID: 33259938]
  • Zhuolin Zhang, Lele Cai, Hong Wu, Xinglu Xu, Wenqing Fang, Xuan He, Xiao Wang, Xin Li. Paricalcitol versus Calcitriol + Cinacalcet for the Treatment of Secondary Hyperparathyroidism in Chronic Kidney Disease in China: A Cost-Effectiveness Analysis. Frontiers in public health. 2021; 9(?):712027. doi: 10.3389/fpubh.2021.712027. [PMID: 34368073]
  • Ronald M Evans, Scott M Lippman. Shining Light on the COVID-19 Pandemic: A Vitamin D Receptor Checkpoint in Defense of Unregulated Wound Healing. Cell metabolism. 2020 11; 32(5):704-709. doi: 10.1016/j.cmet.2020.09.007. [PMID: 32941797]
  • Sandra Rayego-Mateos, Jose Luis Morgado-Pascual, José Manuel Valdivielso, Ana Belén Sanz, Enrique Bosch-Panadero, Raúl R Rodrigues-Díez, Jesús Egido, Alberto Ortiz, Emilio González-Parra, Marta Ruiz-Ortega. TRAF3 Modulation: Novel Mechanism for the Anti-inflammatory Effects of the Vitamin D Receptor Agonist Paricalcitol in Renal Disease. Journal of the American Society of Nephrology : JASN. 2020 09; 31(9):2026-2042. doi: 10.1681/asn.2019111206. [PMID: 32631974]
  • Hasan Sözel, Sadi Köksoy, Sebahat Ozdem, Fatih Yılmaz, Feyza Bora, F Fevzi Ersoy. Lymphocyte and monocyte vitamin D receptor expression during paricalcitol or calcitriol treatments in patients with stage 5 chronic kidney disease. International urology and nephrology. 2020 Aug; 52(8):1563-1570. doi: 10.1007/s11255-020-02475-1. [PMID: 32405698]
  • Hatice Aygun, Nursah Basol, Serdar Savas Gul. Cardioprotective Effect of Paricalcitol on Amitriptyline-Induced Cardiotoxicity in Rats: Comparison of [99mTc]PYP Cardiac Scintigraphy with Electrocardiographic and Biochemical Findings. Cardiovascular toxicology. 2020 08; 20(4):427-436. doi: 10.1007/s12012-020-09569-3. [PMID: 32219715]
  • Carlo Massimetti, Antonio Bellasi, Sandro Feriozzi. [Cholecalciferol supplementation improves secondary hyperparathyroidism control in hemodialysis patients]. Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia. 2020 Jun; 37(3):. doi: . [PMID: 32530156]
  • Dangfeng Zhang, Lin Qiao, Ting Fu. Paricalcitol improves experimental autoimmune encephalomyelitis (EAE) by suppressing inflammation via NF-κB signaling. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2020 May; 125(?):109528. doi: 10.1016/j.biopha.2019.109528. [PMID: 32106388]
  • Ravi I Thadhani, Sophia Rosen, Norma J Ofsthun, Len A Usvyat, Lorien S Dalrymple, Franklin W Maddux, Jeffrey L Hymes. Conversion from Intravenous Vitamin D Analogs to Oral Calcitriol in Patients Receiving Maintenance Hemodialysis. Clinical journal of the American Society of Nephrology : CJASN. 2020 03; 15(3):384-391. doi: 10.2215/cjn.07960719. [PMID: 32111702]
  • Laura Salanova Villanueva, Yohana Gil Giraldo, Begoña Santos Sánchez-Rey, Abelardo Aguilera Peralta. Paricalcitol regulatory effect on inflammatory, fibrotic and anticalcificating parameters in renal patiente. Far beyond mineral bone disease regulation. Nefrologia. 2020 Mar; 40(2):171-179. doi: 10.1016/j.nefro.2019.08.001. [PMID: 31740151]
  • Kamyar Kalantar-Zadeh, Christopher S Hollenbeak, Roy Arguello, Sophie Snyder, Akhtar Ashfaq. The cost-effectiveness of extended-release calcifediol versus paricalcitol for the treatment of secondary hyperparathyroidism in stage 3-4 CKD. Journal of medical economics. 2020 Mar; 23(3):308-315. doi: 10.1080/13696998.2019.1693385. [PMID: 31726882]
  • Graziella D'Arrigo, Patrizia Pizzini, Sebastiano Cutrupi, Rocco Tripepi, Giovanni Tripepi, Francesca Mallamaci, Carmine Zoccali. FGF23 and the PTH response to paricalcitol in chronic kidney disease. European journal of clinical investigation. 2020 Feb; 50(2):e13196. doi: 10.1111/eci.13196. [PMID: 31863599]
  • Zhaoxin Hu, Hao Zhang, Bin Yi, Shikun Yang, Jun Liu, Jing Hu, Jianwen Wang, Ke Cao, Wei Zhang. VDR activation attenuate cisplatin induced AKI by inhibiting ferroptosis. Cell death & disease. 2020 01; 11(1):73. doi: 10.1038/s41419-020-2256-z. [PMID: 31996668]
  • Xinghua Geng, Ermin Shi, Shiwei Wang, Yuzhi Song. A comparative analysis of the efficacy and safety of paricalcitol versus other vitamin D receptor activators in patients undergoing hemodialysis: A systematic review and meta-analysis of 15 randomized controlled trials. PloS one. 2020; 15(5):e0233705. doi: 10.1371/journal.pone.0233705. [PMID: 32470067]
  • Eunjin Bae, Jin Hyun Kim, Myeong Hee Jung, Si Jung Jang, Tae Won Lee, Sehyun Jung, Seunghye Lee, Ha Nee Jang, Se-Ho Chang, Dong Jun Park. Paricalcitol Attenuates Contrast-Induced Acute Kidney Injury by Regulating Mitophagy and Senescence. Oxidative medicine and cellular longevity. 2020; 2020(?):7627934. doi: 10.1155/2020/7627934. [PMID: 33299530]
  • Hege Kampen Pihlstrøm, Thor Ueland, Annika E Michelsen, Pål Aukrust, Franscesca Gatti, Clara Hammarström, Monika Kasprzycka, Junbai Wang, Guttorm Haraldsen, Geir Mjøen, Dag Olav Dahle, Karsten Midtvedt, Ivar Anders Eide, Anders Hartmann, Hallvard Holdaas. Exploring the potential effect of paricalcitol on markers of inflammation in de novo renal transplant recipients. PloS one. 2020; 15(12):e0243759. doi: 10.1371/journal.pone.0243759. [PMID: 33326471]
  • Nakhoul Nakhoul, Tina Thawko, Evgeny Farber, Inbal Dahan, Hagar Tadmor, Rola Nakhoul, Anaam Hanut, Ghasan Salameh, Ibrahim Shagrawy, Farid Nakhoul. The Therapeutic Effect of Active Vitamin D Supplementation in Preventing the Progression of Diabetic Nephropathy in a Diabetic Mouse Model. Journal of diabetes research. 2020; 2020(?):7907605. doi: 10.1155/2020/7907605. [PMID: 33294462]
  • Alexandra Schuster, Akram Al-Makki, Brian Shepler. Use of Paricalcitol as Adjunctive Therapy to Renin-Angiotensin-Aldosterone System Inhibition for Diabetic Nephropathy: A Systematic Review of the Literature. Clinical therapeutics. 2019 11; 41(11):2416-2423. doi: 10.1016/j.clinthera.2019.09.009. [PMID: 31601446]
  • Yan Liu, Liu Li, Bin Yi, Zhao-Xin Hu, Ai-Mei Li, Cheng Yang, Li Zheng, Hao Zhang. Activation of vitamin D receptor attenuates high glucose-induced cellular injury partially dependent on CYP2J5 in murine renal tubule epithelial cell. Life sciences. 2019 Oct; 234(?):116755. doi: 10.1016/j.lfs.2019.116755. [PMID: 31415769]
  • Cristian Rodelo-Haad, Elvira Esquivias-Motta, Francisco Amaral-Neiva, Alejandro Martin-Malo, Pedro Aljama, Mariano Rodriguez. Reversing extraosseous calcifications. A case of breast uremic calcific arteriolopathy. The breast journal. 2019 09; 25(5):998-999. doi: 10.1111/tbj.13389. [PMID: 31187553]
  • Kristina Lundwall, Josefin Mörtberg, Fariborz Mobarrez, Stefan H Jacobson, Gun Jörneskog, Jonas Spaak. Changes in microparticle profiles by vitamin D receptor activation in chronic kidney disease - a randomized trial. BMC nephrology. 2019 08; 20(1):290. doi: 10.1186/s12882-019-1445-4. [PMID: 31370809]
  • Hasan Koc, Hasan Hoser, Yalcin Akdag, Cemaliye Kendir, F Fevzi Ersoy. Treatment of secondary hyperparathyroidism with paricalcitol in patients with end-stage renal disease undergoing hemodialysis in Turkey: an observational study. International urology and nephrology. 2019 Jul; 51(7):1261-1270. doi: 10.1007/s11255-019-02175-5. [PMID: 31161518]
  • Ming-Chao He, Zhe Shi, Nan-Nan Sha, Nan Chen, Shi-Yu Peng, Duan-Fang Liao, Man-Sau Wong, Xiao-Li Dong, Yong-Jun Wang, Ti-Fei Yuan, Yan Zhang. Paricalcitol alleviates lipopolysaccharide-induced depressive-like behavior by suppressing hypothalamic microglia activation and neuroinflammation. Biochemical pharmacology. 2019 05; 163(?):1-8. doi: 10.1016/j.bcp.2019.01.021. [PMID: 30703351]
  • Jie Du, Siqing Jiang, Zhaoxin Hu, Shiqi Tang, Yue Sun, Jinrong He, Zhi Li, Bin Yi, Jianwen Wang, Hao Zhang, Yan Chun Li. Vitamin D receptor activation protects against lipopolysaccharide-induced acute kidney injury through suppression of tubular cell apoptosis. American journal of physiology. Renal physiology. 2019 05; 316(5):F1068-F1077. doi: 10.1152/ajprenal.00332.2018. [PMID: 30864841]
  • Graziella D'arrigo, Patrizia Pizzini, Sebastiano Cutrupi, Rocco Tripepi, Giovanni Tripepi, Francesca Mallamaci, Carmine Zoccali. Vitamin D receptor activation raises soluble thrombomodulin levels in chronic kidney disease patients: a double blind, randomized trial. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 2019 05; 34(5):819-824. doi: 10.1093/ndt/gfy085. [PMID: 29668990]
  • Ricardo Villa-Bellosta, Ignacio Mahillo-Fernández, Alberto Ortíz, Emilio González-Parra. Questioning the Safety of Calcidiol in Hemodialysis Patients. Nutrients. 2019 04; 11(5):. doi: 10.3390/nu11050959. [PMID: 31035488]
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