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Mitochondrial Dysfunction in Cardiorenal Syndrome 3: Renocardiac Effect of Vitamin C
Raquel Silva Neres-Santos1, Carolina Victoria Cruz Junho1, Karine Panico1
1Laboratory of Cardiovascular Immunology, Center of Natural and Human Sciences (CCNH), Federal University of ABC, Santo André 09210-580, Brazil.
Insights
Vitamin C protects kidneys and offers benefits to the heart in a cardiorenal syndrome model. This antioxidant may prevent damage caused by kidney or heart insults.
Area of Science:
- Cardiorenal medicine
- Mitochondrial pathophysiology
- Antioxidant research
Background:
- Cardiorenal syndrome (CRS) involves kidney-heart interactions, with Type 3 CRS (CRS3) featuring acute kidney injury preceding cardiac issues.
- Mitochondrial dysfunction and oxidative stress are key in CRS3.
- Vitamin C, a known antioxidant, shows protective effects on cardiac, renal, and vascular tissues.
Purpose of the Study:
- To investigate vitamin C's protective effects on kidneys and heart in an in vivo CRS3 model.
- To evaluate vitamin C's impact on renal function, mitochondrial activity, and oxidative stress markers post-ischemia-reperfusion (IR).
Main Methods:
- Unilateral renal ischemia and reperfusion (IR) in mice, with and without vitamin C treatment.
- Assessment of kidney and heart tissues, including morphometry, serum markers (urea, creatinine), respirometry, NO levels, and gene expression (mitochondrial dynamics, NOS).
Main Results:
- IR led to reduced kidney weight, impaired renal function, decreased mitochondrial oxygen consumption, elevated NO, and altered Mfn2 expression.
- Cardiac function showed reduced oxygen consumption and NO levels post-IR.
- Vitamin C treatment preserved kidney function, reduced NO, modulated NOS expression, and improved oxygen consumption in both organs.
Conclusions:
- Vitamin C demonstrates protective effects on kidneys and beneficial impacts on the heart following IR injury.
- Vitamin C may serve as a preventive strategy against cardiorenal insults in CRS3.
Abstract:
Cardiorenal syndrome (CRS) is a pathological link between the kidneys and heart, in which an insult in a kidney or heart leads the other organ to incur damage. CRS is classified into five subtypes, and type 3 (CRS3) is characterized by acute kidney injury as a precursor to subsequent cardiovascular changes. Mitochondrial dysfunction and oxidative and nitrosative stress have been reported in the pathophysiology of CRS3. It is known that vitamin C, an antioxidant, has proven protective capacity for cardiac, renal, and vascular endothelial tissues. Therefore, the present study aimed to assess whether vitamin C provides protection to heart and the kidneys in an in vivo CRS3 model. The unilateral renal ischemia and reperfusion (IR) protocol was performed for 60 min in the left kidney of adult mice, with and without vitamin C treatment, immediately after IR or 15 days after IR. Kidneys and hearts were subsequently collected, and the following analyses were conducted: renal morphometric evaluation, serum urea and creatinine levels, high-resolution respirometry, amperometry technique for NO measurement, gene expression of mitochondrial dynamic markers, and NOS. The analyses showed that the left kidney weight was reduced, urea and creatinine levels were increased, mitochondrial oxygen consumption was reduced, NO levels were elevated, and Mfn2 expression was reduced after 15 days of IR compared to the sham group. Oxygen consumption and NO levels in the heart were also reduced. The treatment with vitamin C preserved the left kidney weight, restored renal function, reduced NO levels, decreased iNOS expression, elevated constitutive NOS isoforms, and improved oxygen consumption. In the heart, oxygen consumption and NO levels were improved after vitamin C treatment, whereas the three NOS isoforms were overexpressed. These data indicate that vitamin C provides protection to the kidneys and some beneficial effects to the heart after IR, indicating it may be a preventive approach against cardiorenal insults.
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