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Platelet-based Detection of Nitric Oxide in Blood by Measuring VASP Phosphorylation
Published on: January 7, 2019
Decreased platelet nitric oxide synthase activity and plasma nitric oxide metabolites in major depressive disorder
Wendy E Chrapko1, Paul Jurasz, Marek W Radomski
1Department of Psychiatry, University of Alberta, Edmonton, Alberta, Canada.
Insights
Major depression is linked to higher cardiovascular risk due to reduced nitric oxide (NO) production in patients. This study found lower plasma nitric oxide metabolites and platelet endothelial NO synthase activity in those with depression.
Area of Science:
- Cardiovascular Medicine
- Psychiatry
- Biochemistry
Background:
- Major depression (MD) is an independent risk factor for coronary heart disease (CHD).
- The underlying mechanisms linking MD and CHD are not fully understood.
- Nitric oxide (NO) is crucial for cardiovascular regulation, and reduced NO production is linked to cardiovascular risk factors.
Purpose of the Study:
- To investigate the hypothesis that patients with MD exhibit reduced nitric oxide (NO) production by platelets and endothelium compared to healthy controls (HCs).
Main Methods:
- Analyzed plasma nitric oxide metabolite (NOx) levels using chemiluminescence.
- Assessed platelet endothelial NO synthase (eNOS) activity by measuring the conversion of L-[(14)C]arginine to L-[(14)C]citrulline.
- Included 15 subjects with MD and 16 HCs.
Main Results:
- Significantly lower plasma NOx levels were observed in subjects with MD compared to HCs.
- Platelet eNOS activity was also significantly reduced in subjects with MD versus HCs.
Conclusions:
- Decreased nitric oxide (NO) production by the vascular wall and platelets may contribute to the elevated CHD risk in individuals with major depression (MD).
- These findings highlight a potential biochemical link between depression and cardiovascular disease.
Background:
Major depression (MD) has been associated with increased cardiovascular mortality in patients with coronary heart disease (CHD) and has been described as an independent risk factor for the development of CHD in healthy subjects; however, the mechanism of the association between MD and CHD remains to be determined. Nitric oxide (NO) plays a major role in cardiovascular regulation, and decreased NO production has been associated with several cardiovascular risk factors. We hypothesized that in patients with MD, NO production by both platelets and the endothelium would be reduced when compared with healthy control subjects (HCs).
Methods:
Blood samples were obtained from 15 subjects with MD and 16 HCs with no known history of cardiovascular illness. Plasma NO metabolite (NOx) levels were analyzed by chemiluminescence. Platelet endothelial NO synthase (eNOS) activity was examined through the conversion of l-[(14)C]arginine to l-[(14)C]citrulline.
Results:
The levels of both plasma NOx and platelet eNOS activity were significantly lower in subjects with MD compared with HCs.
Conclusions:
These data suggest that decreased NO production by the vascular wall and platelets might contribute to the increased CHD risk observed in patients with MD.
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