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Review
. 2020 Jul;40(4):1147-1177.
doi: 10.1002/med.21650. Epub 2019 Dec 9.

Carbon monoxide: An emerging therapy for acute kidney injury

Affiliations
Review

Carbon monoxide: An emerging therapy for acute kidney injury

Xiaoxiao Yang et al. Med Res Rev. 2020 Jul.

Abstract

Treating acute kidney injury (AKI) represents an important unmet medical need both in terms of the seriousness of this medical problem and the number of patients. There is also a large untapped market opportunity in treating AKI. Over the years, there has been much effort in search of therapeutics with minimal success. However, over the same time period, new understanding of the underlying pathobiology and molecular mechanisms of kidney injury have undoubtedly helped the search for new therapeutics. Along this line, carbon monoxide (CO) has emerged as a promising therapeutic agent because of its demonstrated cytoprotective, and immunomodulatory effects. CO has also been shown to sensitize cancer, but not normal cells, to chemotherapy. This is particularly important in treating cisplatin-induced AKI, a common clinical problem that develops in patients receiving cisplatin therapies for a number of different solid organ malignancies. This review will examine and make the case that CO be developed into a therapeutic agent against AKI.

Keywords: CO-releasing molecules; acute kidney injury; carbon monoxide; nephrotoxicity; organic CO prodrugs.

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Figures

Figure 1.
Figure 1.
Compounds known to induce AKI.
Figure 2.
Figure 2.
Formation of cysteine S-cisplatin conjugates. (Summarized based on related reports and reviews,)
Figure 3.
Figure 3.
Metabolic activation of AA and formation of DNA adducts.
Figure 4.
Figure 4.
The general design and representative compounds of the organic CO prodrugs.
Figure 5.
Figure 5.
Other reported organic CO donors.

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References

    1. Chawla LS, Bellomo R, Bihorac A, Goldstein SL, Siew ED, Bagshaw SM, Bittleman D, Cruz D, Endre Z, Fitzgerald RL, Forni L, Kane-Gill SL, Hoste E, Koyner J, Liu KD, Macedo E, Mehta R, Murray P, Nadim M, Ostermann M, Palevsky PM, Pannu N, Rosner M, Wald R, Zarbock A, Ronco C, Kellum JA. Acute kidney disease and renal recovery: consensus report of the Acute Disease Quality Initiative (ADQI) 16 Workgroup. Nat Rev Nephrol. 2017;13:241–257. - PubMed
    1. Rewa O, Bagshaw SM. Acute kidney injury-epidemiology, outcomes and economics. Nature reviews Nephrology. 2014;10:193–207. - PubMed
    1. Hoste EAJ, Kellum JA, Selby NM, Zarbock A, Palevsky PM, Bagshaw SM, Goldstein SL, Cerda J, Chawla LS. Global epidemiology and outcomes of acute kidney injury. Nat Rev Nephrol. 2018;14:607–625. - PubMed
    1. Bellomo R, Kellum JA, Ronco C. Acute kidney injury. Lancet (London, England). 2012;380:756–766. - PubMed
    1. Billings FTt, Shaw AD. Clinical trial endpoints in acute kidney injury. Nephron Clin Pract. 2014;127:89–93. - PMC - PubMed

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