tetano
Editor, Senior Moderator
Nitric Oxide
. 2022 Jan 12;120:16-25.
doi: 10.1016/j.niox.2022.01.002. Online ahead of print.
Renal consequences of the novel coronavirus disease 2019 (COVID-19) and hydrogen sulfide as a potential therapy
George J Dugbartey[SUP] 1 [/SUP], Karl K Alornyo[SUP] 2 [/SUP], Bright O Ohene[SUP] 2 [/SUP], Vincent Boima[SUP] 3 [/SUP], Sampson Antwi[SUP] 4 [/SUP], Alp Sener[SUP] 5 [/SUP]
Affiliations
Abstract
The novel coronavirus disease 2019 (COVID-19), caused by SARS-CoV-2, is a global pandemic which is primarily considered a respiratory illness. However, emerging reports show that the virus exhibits both pulmonary and extra-pulmonary manifestations in humans, with the kidney as a major extra-pulmonary target due to its abundant expression of angiotensin-converting enzyme 2 and transmembrane protease serine 2, which facilitate entry of the virus into cells. Acute kidney injury has become prevalent in COVID-19 patients without prior any history of kidney dysfunction. In addition, the virus also worsens kidney conditions and increases mortality of COVID-19 patients with pre-existing chronic kidney disease, renal cancer, diabetic nephropathy, end-stage kidney disease as well as dialysis and kidney transplant patients. In the search for antiviral agents for the treatment of COVID-19, hydrogen sulfide (H[SUB]2[/SUB]S), the third established member of gasotransmitter family, is emerging as a potential candidate, possessing important therapeutic properties including antiviral, anti-inflammatory, anti-thrombotic and antioxidant properties. A recent clinical study revealed higher serum H[SUB]2[/SUB]S levels in survivors of COVID-19 pneumonia with reduced interleukin-6 levels compared to fatal cases. In this review, we summarize the global impact of COVID-19 on kidney conditions and discuss the emerging role of H[SUB]2[/SUB]S as a potential COVID-19 therapy.
Keywords: Angiotensin-converting enzyme 2 (ACE2); Coronavirus disease 2019 (COVID-19); H(2)S donors; Hydrogen sulfide (H(2)S); Kidney; SARS-CoV-2.
. 2022 Jan 12;120:16-25.
doi: 10.1016/j.niox.2022.01.002. Online ahead of print.
Renal consequences of the novel coronavirus disease 2019 (COVID-19) and hydrogen sulfide as a potential therapy
George J Dugbartey[SUP] 1 [/SUP], Karl K Alornyo[SUP] 2 [/SUP], Bright O Ohene[SUP] 2 [/SUP], Vincent Boima[SUP] 3 [/SUP], Sampson Antwi[SUP] 4 [/SUP], Alp Sener[SUP] 5 [/SUP]
Affiliations
- PMID: 35032641
- PMCID: PMC8755416
- DOI: 10.1016/j.niox.2022.01.002
Abstract
The novel coronavirus disease 2019 (COVID-19), caused by SARS-CoV-2, is a global pandemic which is primarily considered a respiratory illness. However, emerging reports show that the virus exhibits both pulmonary and extra-pulmonary manifestations in humans, with the kidney as a major extra-pulmonary target due to its abundant expression of angiotensin-converting enzyme 2 and transmembrane protease serine 2, which facilitate entry of the virus into cells. Acute kidney injury has become prevalent in COVID-19 patients without prior any history of kidney dysfunction. In addition, the virus also worsens kidney conditions and increases mortality of COVID-19 patients with pre-existing chronic kidney disease, renal cancer, diabetic nephropathy, end-stage kidney disease as well as dialysis and kidney transplant patients. In the search for antiviral agents for the treatment of COVID-19, hydrogen sulfide (H[SUB]2[/SUB]S), the third established member of gasotransmitter family, is emerging as a potential candidate, possessing important therapeutic properties including antiviral, anti-inflammatory, anti-thrombotic and antioxidant properties. A recent clinical study revealed higher serum H[SUB]2[/SUB]S levels in survivors of COVID-19 pneumonia with reduced interleukin-6 levels compared to fatal cases. In this review, we summarize the global impact of COVID-19 on kidney conditions and discuss the emerging role of H[SUB]2[/SUB]S as a potential COVID-19 therapy.
Keywords: Angiotensin-converting enzyme 2 (ACE2); Coronavirus disease 2019 (COVID-19); H(2)S donors; Hydrogen sulfide (H(2)S); Kidney; SARS-CoV-2.