Biochemistry & Physiology: Open Access
Open Access

Oxidative stress; Cardiovascular diseases; Aging; Mitochondrial dysfunction; Endothelial dysfunction; Inflammation; Lipid peroxidation

Introduction

Cardiovascular diseases remain the leading cause of morbidity and mortality globally. Aging is a primary risk factor for CVDs, with the incidence increasing significantly in older populations [1]. Oxidative stress is a critical factor that accelerates the aging process and the development of CVDs. This review provides an in-depth analysis of the role of oxidative stress in age-related CVDs, highlighting the underlying biochemical mechanisms and potential therapeutic approaches [2,3].

Oxidative stress: an overview

Oxidative stress occurs when there is an imbalance between ROS production and antioxidant defenses. ROS, including superoxide anions, hydrogen peroxide, and hydroxyl radicals, are byproducts of normal cellular metabolism [4]. While low levels of ROS play roles in cell signaling and homeostasis, excessive ROS can damage cellular components, including lipids, proteins, and DNA, leading to pathological conditions.

Mechanisms of oxidative stress in cardiovascular aging

Mitochondrial dysfunction

Mitochondria are the primary source of ROS in cells. With aging, mitochondrial function declines, leading to increased ROS production [5]. Mitochondrial DNA (mtDNA) is particularly susceptible to oxidative damage, which can impair the electron transport chain and further enhance ROS generation.

Endothelial dysfunction

The endothelium regulates vascular tone and homeostasis. Oxidative stress impairs endothelial function by reducing the bioavailability of nitric oxide (NO), a potent vasodilator [6]. Reduced NO levels contribute to vascular stiffness and hypertension, common in aging populations.

Inflammation

Chronic low-grade inflammation, often termed inflammaging, is prevalent in older adults.

ROS can activate pro-inflammatory signaling pathways, leading to increased production of inflammatory cytokines, which further exacerbate oxidative stress and vascular damage.

Lipid peroxidation

Oxidative stress induces lipid peroxidation, generating reactive lipid species that can modify proteins and nucleic acids [7]. These modifications contribute to the pathogenesis of atherosclerosis by promoting plaque formation and instability.

Age-related cardiovascular diseases and oxidative stress

Atherosclerosis

Atherosclerosis is characterized by the accumulation of lipid-laden plaques in arterial walls. Oxidative stress accelerates atherogenesis by promoting the oxidation of low-density lipoprotein (LDL) and endothelial dysfunction.

Hypertension

Hypertension, or high blood pressure, is prevalent in aging populations and is a major risk factor for CVDs. Oxidative stress reduces NO availability and promotes vasoconstriction, contributing to increased blood pressure.

Heart failure

Heart failure occurs when the heart is unable to pump blood efficiently, leading to inadequate tissue perfusion. Oxidative stress contributes to myocardial dysfunction through direct damage to cardiomyocytes and by promoting fibrosis [8].

Therapeutic interventions

Antioxidants

Antioxidants such as vitamins C and E, polyphenols, and coenzyme Q10 can neutralize ROS and reduce oxidative damage. Clinical trials investigating the efficacy of antioxidants in CVDs have yielded mixed results, highlighting the need for targeted therapies.

Mitochondrial-targeted therapies

Compounds like MitoQ and SkQ1 specifically target mitochondrial ROS, offering potential benefits in mitigating mitochondrial dysfunction [9].

Lifestyle interventions

Diet, exercise, and smoking cessation can reduce oxidative stress and improve cardiovascular health.

Diets rich in antioxidants, such as the Mediterranean diet, have been associated with reduced CVD risk.

Pharmacological agents

Statins, commonly used for lowering cholesterol, also exhibit antioxidant properties.

Angiotensin-converting enzyme (ACE) inhibitors and angiotensin II receptor blockers (ARBs) reduce oxidative stress by modulating the renin-angiotensin system [10].

Discussion

The role of oxidative stress in age-related cardiovascular diseases (CVDs) is multifaceted and complex. This discussion delves into the implications of the findings presented in this review, the challenges in targeting oxidative stress, and future directions for research and clinical practice.

Implications of oxidative stress in cardiovascular aging

The evidence underscores that oxidative stress is a critical mediator in the development and progression of various agerelated CVDs. Mitochondrial dysfunction, endothelial dysfunction, chronic inflammation, and lipid peroxidation are key mechanisms through which oxidative stress exerts its detrimental effects on the cardiovascular system.

Mitochondrial dysfunction and cardiovascular aging

Mitochondrial dysfunction leads to excessive ROS production, contributing to cellular and tissue damage in the cardiovascular system. The accumulation of oxidative damage in mitochondrial DNA and proteins disrupts normal cellular function and promotes cell death, exacerbating heart failure and other CVDs.

Endothelial dysfunction

The reduction in NO bioavailability due to oxidative stress is a significant factor in vascular aging. NO is essential for maintaining vascular tone and preventing thrombosis. Its reduction leads to hypertension and atherosclerosis, highlighting the importance of targeting endothelial function in therapeutic strategies.

Inflammation and oxidative stress

The interplay between oxidative stress and inflammation creates a vicious cycle that perpetuates vascular damage. ROS can activate pro-inflammatory pathways, leading to chronic inflammation, which in turn increases oxidative stress. This cycle is particularly evident in atherosclerosis, where inflammatory cells and cytokines contribute to plaque instability.

Lipid peroxidation

The oxidative modification of lipids, particularly LDL, is a hallmark of atherosclerosis. Oxidized LDL is taken up by macrophages, forming foam cells and promoting plaque formation. Targeting lipid peroxidation processes could be a viable approach to mitigate atherosclerosis progression.

Challenges in targeting oxidative stress

Despite the clear role of oxidative stress in CVDs, clinical trials using antioxidants have produced mixed results. This inconsistency may stem from several factors:

Timing and dosage

The timing of antioxidant administration is crucial. Antioxidants may be more effective in the early stages of CVDs rather than in advanced stages where irreversible damage has occurred. Additionally, optimal dosages need to be determined to avoid potential pro-oxidant effects at high concentrations.

Specificity

Broad-spectrum antioxidants may not be as effective as targeted therapies. Mitochondria-specific antioxidants like MitoQ have shown promise, suggesting that more precise targeting of ROS sources could yield better outcomes.

Biomarkers

Identifying reliable biomarkers for oxidative stress and antioxidant efficacy is essential for personalizing treatment. Current biomarkers may not accurately reflect the oxidative state in different tissues or stages of disease.

Future Directions

To advance the understanding and treatment of oxidative stress in age-related CVDs, several avenues of research should be pursued

Mitochondrial Therapies

Further investigation into mitochondrial-targeted antioxidants and modulators of mitochondrial function is warranted. These therapies have the potential to reduce ROS production at the source and improve cellular energy metabolism.

Gene therapy

Gene therapy approaches to enhance endogenous antioxidant defenses or repair damaged mtDNA could offer long-term solutions for mitigating oxidative stress.

Combination therapies

Combining antioxidants with other pharmacological agents, such as anti-inflammatory drugs or statins, may enhance therapeutic efficacy. Exploring synergistic effects could provide comprehensive protection against oxidative stress and inflammation.

Lifestyle interventions

Continued emphasis on lifestyle modifications, including diet, exercise, and smoking cessation, is critical. Research should focus on optimizing these interventions to maximize their antioxidant potential and cardiovascular benefits.

Personalized medicine

Advances in genomics and metabolomics can facilitate personalized approaches to managing oxidative stress. Understanding individual variations in oxidative stress responses and antioxidant needs can lead to more effective and tailored treatments.

Conclusion

Oxidative stress is a pivotal factor in the pathogenesis of agerelated cardiovascular diseases. While challenges remain in effectively targeting oxidative stress, ongoing research offers hope for developing more precise and effective therapeutic strategies. By addressing the underlying mechanisms and exploring innovative treatments, it is possible to mitigate the impact of oxidative stress on cardiovascular health in aging populations. Future research should continue to unravel the complexities of oxidative stress and translate these insights into clinical practice to improve outcomes for individuals with agerelated CVDs.

References

1. Takahashi S, Mizukami K, Yasuno F, Asada T (2009) Depression associated with dementia with Lewy bodies (DLB) and the effect of somatotherapy.Psychogeriatrics 9: 56-61.

Indexed at, Google Scholar, Crossref

2. leMaire A, Grimaldi M, Roecklin D, Dagnino S, Vivat-Hannah V, et al. (2009)Activation of RXR-PPAR heterodimers by organotin environmental endocrine disruptors. EMBO Rep 10: 367-373.

Indexed at, Google Scholar, Crossref

3. Carter CS, Barch DM (2007) Cognitive neuroscience-based approaches to measuring and improving treatment effects on cognition in schizophrenia: the CNTRICS initiative. Schizophr Bull 33: 1131-1137.

Indexed at, Google Scholar, Crossref

4. Nakanishi T (2008)Endocrine disruption induced by organotin compounds: Organotins function as a powerful agonist for nuclear receptors rather than aromatase inhibitor. J Toxicol Sci 33: 269-276.

Indexed at, Google Scholar, Crossref

5. Brtko J, Dvorak Z (2015)Triorganotin compounds-Ligands for “rexinoid” inducible transcription factors: Biological effects.Toxicol Lett 234: 50-58.

Indexed at, Google Scholar, Crossref

6. Bauer JM, Verlaan S, Bautmans I, Brandt K, Donini LM, et al. (2015) Effects of a vitamin D and leucine-enriched whey protein nutritional supplement on measures of sarcopenia in older adults, the PROVIDE study: a randomized, double-blind, placebo-controlled trial. J Am Med Dir Assoc 16: 740–747.

Indexed at, Google Scholar, Crossref

7. Bodo J, Hunakova L, Kvasnicka P, Jakubikova J, Duraj J (2006)Sensitization for cisplatin-induced apoptosis by isothiocyanate E-4IB leads to signaling pathways alterations.Br J Cancer 95: 1348–1353.

Indexed at, Google Scholar, Crossref

8. Oddie A, Wyllie K (2004) Measurement of urine output by weighing nappies.Archives of Disease in Childhood. Fetal and Neonatal Edition 89: 180-1181.

Indexed at, Google Scholar, Crossref

9. Unger FT, Klasen HA, Tchartchian G, Wilde RL, Witte I, et al. (2009)DNA damage induced by cis- and carboplatin as indicator for in vitro sensitivity of ovarian carcinoma cells. BMC Cancer 9: 359.

Indexed at, Google Scholar, Crossref

10. Dolin RH, Boxwala A (2018) A pharmacogenomics clinical decision support service based on FHIR and CDS Hooks. Methods Inf Med 57: 77-80.

Indexed at, Google Scholar, Crossref