[Neutrophile apoptosis in patients with chronic rheumatic heart disease]

Insights

In chronic rheumatic disease (CRD), neutrophile granulocytes show heightened metabolism but reduced nitric oxide (NO) synthesis and apoptosis. Stimulating NO production may reduce oxidative stress and stabilize CRD.

Area of Science:

  • Immunology
  • Cardiovascular Medicine
  • Rheumatology

Context:

  • Chronic rheumatic disease (CRD) often involves cardiovascular complications.
  • Cardiovascular pathology in CRD includes valvular defects, arterial hypertension (AH), and cardiac arrhythmias.
  • Understanding neutrophile function is crucial in CRD with cardiovascular involvement.

Purpose:

  • To investigate neutrophile granulocyte functioning in patients with CRD and cardiovascular pathology.
  • To assess nitric oxide (NO) production, functional cell activity, and apoptotic readiness in these patients.
  • To explore the role of NO synthesis as a protective mechanism.

Summary:

  • Patients with CRD exhibited intensified oxygen-dependent neutrophile metabolism, increased reserve capacity, but decreased NO synthesis and apoptotic activity.
  • Arterial hypertension correlated with lowered neutrophile nitric oxide production.
  • Paroxysmal cardiac fibrillation showed intensified active oxygen metabolite production, indicating pro-oxidative system hyperactivity and potential myocardial damage.

Impact:

  • Neutrophils in CRD patients were in a primed state with high biocidal potential and reduced apoptotic readiness, indicating high mobilization.
  • Nitric oxide (NO) synthesis acts as a protective autoregulation factor against phagocyte cytotoxic activity.
  • Stimulating granulocyte NO production presents a potential therapeutic strategy to mitigate oxidative stress, reduce leukocyte aggression, and stabilize CRD progression.

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