Investigating the Ischaemic Phase of Skin NADH Fluorescence Dynamics in Recently Diagnosed Primary Hypertension: A Time Series Analysis

Author:

Pawlak-Chomicka Regina1,Chomicki Wojciech2,Krauze Tomasz3,Uruski Paweł1,Guzik Maria4ORCID,Piskorski Jarosław5ORCID,Tykarski Andrzej1,Guzik Przemysław3ORCID

Affiliation:

1. Department of Hypertensiology, Angiology and Internal Medicine, Poznan University of Medical Sciences, 61-848 Poznan, Poland

2. Department of Physics of Functional Materials, Faculty of Physics, Adam Mickiewicz University, 61-614 Poznan, Poland

3. Department of Cardiology-Intensive Therapy and Internal Medicine, Poznan University of Medical Sciences, 60-355 Poznan, Poland

4. Faculty of Biology, Medicine and Health Sciences, University of Manchester, Manchester M13 9PL, UK

5. Institute of Physics, University of Zielona Gora, 65-516 Zielona Gora, Poland

Abstract

The reduced form of nicotinamide adenine dinucleotide (NADH) is crucial in cellular metabolism. During hypoxia, NADH accumulation results from anaerobic cytoplasmic glycolysis and impaired mitochondrial function. This study aimed to compare the dynamic changes in the 460-nm forearm skin fluorescence, which reflects cellular NADH content, during transient ischaemia between healthy individuals and patients with newly diagnosed, untreated essential hypertension (HA). Sixteen healthy volunteers and sixty-five patients with HA underwent non-invasive measurement of forearm skin NADH content using the Flow Mediated Skin Fluorescence (FMSF) method at rest and during a 100-s transient ischaemia induced by inflation of the brachial cuff. The fluorescent signal was sampled at 25 Hz. All samples were normalised to the end of the ischaemic phase, which is the most stable phase of the whole recording. Slope values of 1 s linear regressions were determined for every 25-sample neighbouring set. The 1-s slopes in the early phase of skin ischaemia, indicating quicker hypoxia-induced NADH accumulation in skin, were significantly higher in patients with HA than in healthy individuals. These findings suggest that some protecting mechanisms postponing the early consequences of early cellular hypoxia and premature NADH accumulation during skin ischaemia are impaired in patients with untreated HA. Further studies are needed to investigate this phenomenon.

Funder

National Center for Research and Development in Poland

European Regional Development Fund under the Smart Growth Operational Program

Publisher

MDPI AG

Subject

General Medicine

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