Marinobufagenin
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IUPAC name
3β,5-Dihydroxy-14,15-epoxy-5β,14β-bufa-20,22-dienolide
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Systematic IUPAC name
5-[(1R,2aR,3aS,3bR,5aS,7S,9aR,9bS,11aR)-5b,7-Dihydroxy-9a,11a-dimethylhexadecahydronaphtho[1′,2′:6,7]indeno[1,7a-b]oxiren-1-yl]-2H-pyran-2-one | |
Other names
Marinobufagin, Marinobufagenin
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C24H32O5 | |
Molar mass | 400.515 g·mol−1 |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
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Toxic |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Marinobufagenin (marinobufagin, MBG) is a cardiotonic bufadienolide steroid.[1] It is secreted by the toad species such as Bufo marinus.[1] It also can be found in the plasma and urine of human subjects with myocardial infarction, kidney failure, heart failure, and preeclampsia.[2][3][4][5] MBG is a vasoconstrictor and a sodium–potassium adenosine triphosphatase (Na/K-ATPase) inhibitor with a high affinity for the alpha-1 isoform of the enzyme, the main isoform in the vascular wall and the kidney.[6]
It is produced by adrenal cortex and placenta via CYP27a1 pathway.[7] MBG regulates the monovalent ions balance and cell homeostasis, and by binding to the Na/K-ATPase, it affects cell growth and differentiation, apoptosis, and proliferation.[8] A novel effect of MBG is their ability to induce intracellular signaling, leading to a loss of elasticity and vascular fibrosis.[9]
One of the mechanisms of the pro-fibrotic effect of MBG is the inhibition of the activity of Fli1, a nuclear transcription factor and a negative regulator of collagen 1 synthesis. Fli1 competes with another transcription factor, ETS-1, to maintain a balance between stimulation and repression of the collagen-1 gene. The Na/K ATPase/Src/EGFR complex emerges as a signal cascade, which activates phospholipase C, resulting in the phosphorylation of PKCδ and its translocation to the nucleus. In the nucleus, PKCδ phosphorylates Fli1, which withdraws the Fli1-induced inhibition of the collagen-1 promoter and increases procollagen expression and collagen production.[10]
The antagonism of the pressor and profibrotic effects of MBG by monoclonal anti-MBG antibodies may lead to the prevention of vascular fibrosis in patients with end-stage renal disease and preeclampsia.[11]
References
[edit]- ^ a b Butler, VP Jr.; Morris, JF; Akizawa, T; et al. (1996). "Heterogeneity and lability of endogenous digitalis-like substances in the plasma of the toad, Bufo marinus". American Journal of Physiology. 271 (2): R325 – R332. doi:10.1152/ajpregu.1996.271.2.R325. PMID 8770130.
- ^ Bagrov, AY; Fedorova, OV; Dmitrieva, RI; et al. (1998). "Bufodienolide nature of endogenous inhibitor of Na/K ATPase in the urine from patients with acute myocardial infarction". Hypertension. 31 (5): 1097–1103. doi:10.1161/01.HYP.31.5.1097. PMID 9576120.
- ^ Kolmakova, EV; Haller, ST; Kennedy, DJ; et al. (2011). "Endogenous cardiotonic steroids in chronic renal failure". Nephrology, Dialysis and Transplantation. 26 (9): 2912–2919. doi:10.1093/ndt/gfq772. PMC 3203407.
- ^ Fridman, AI; Matveev, SA; Agalakova, NI; et al. (2002). "Marinobufagenin, an endogenous ligand of alpha-1 Na/K-ATPase, is a marker of congestive heart failure severity". Journal of Hypertension. 20 (6): 1189–1194. doi:10.1097/00004872-200206000-00032. PMID 12023690.
- ^ Nikitina, ER; Mikhailov, AV; Nikandrova, ES; et al. (2011). "In preeclampsia endogenous cardiotonic steroids induce vascular fibrosis and impair relaxation of umbilical arteries". Journal of Hypertension. 29 (4): 769–776. doi:10.1097/HJH.0b013e32834436a7. PMC 3053428. PMID 21330936.
- ^ Bagrov, AY; Shapiro, JI; Fedorova, OV (2009). "Endogenous cardiotonic steroids: physiology, pharmacology and novel therapeutic targets". Pharmacological Reviews. 61 (1): 9–38. doi:10.1124/pr.108.000711. PMC 2763610. PMID 19325075.
- ^ Fedorova, OV; Zernetkina, VI; Shilova, VY; et al. (2015). "Synthesis of an endogenous steroidal Na pump inhibitor marinobufagenin, implicated in human cardiovascular diseases, is initiated by CYP27A1 via bile acid pathway". Circulation: Cardiovascular Genetics. 8 (5): 736–745. doi:10.1161/CIRCGENETICS.115.001217. PMC 4618091. PMID 26374826.
- ^ Fedorova, OV; Shilova, VY; Marshall, CA; et al. (2023). "Silencing of PKG1 gene sensitizes vascular smooth muscle cells to pro-fibrotic effect of marinobufagenin and mimics effect of aging". Journal of the American Heart Association 20. 12 (12): e028768. doi:10.1161/JAHA.122.028768. PMC 10356040. PMID 37301747.
- ^ Kennedy, David J.; Vetteth, Sandeep; Periyasamy, Sankaridrug M.; Kanj, Mohamed; Fedorova, Larisa; Khouri, Samer; Kahaleh, M. Bashar; Xie, Zijian; Malhotra, Deepak; Kolodkin, Nikolai I.; Lakatta, Edward G.; Fedorova, Olga V.; Bagrov, Alexei Y.; Shapiro, Joseph I. (2006). "Central Role for the Cardiotonic Steroid Marinobufagenin in the Pathogenesis of Experimental Uremic Cardiomyopathy". Hypertension. 47 (3): 488–495. doi:10.1161/01.hyp.0000202594.82271.92. PMID 16446397.
- ^ Fedorova, Olga V.; Emelianov, Igor V.; Bagrov, Konstantin A.; Grigorova, Yulia N.; Wei, Wen; Juhasz, Ondrej; Frolova, Elena V.; Marshall, Courtney A.; Lakatta, Edward G.; Konradi, Alexandra O.; Bagrov, Alexei Y. (2015). "Marinobufagenin-induced vascular fibrosis is a likely target for mineralocorticoid antagonists". Journal of Hypertension. 33 (8): 1602–1610. doi:10.1097/HJH.0000000000000591. PMC 4547457. PMID 26136067.
- ^ Agalakova, Natalia I.; Mikhailova, Elena V.; Ershov, Ivan A.; Nadei, Olga V.; Pyankov, Arseny A.; Galagoudza, Michael M.; Adair, C. David; Romanova, Irina V.; Bagrov, Alexei Y. (2024). "Antibody to Endogenous Cardiotonic Steroid Reverses Vascular Fibrosis and Restores Vasorelaxation in Chronic Kidney Disease". International Journal of Molecular Sciences. 25 (16): 8896. doi:10.3390/ijms25168896. PMC 11354990. PMID 39201581.