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Dielectric relaxation of a protein–water system in atherosclerotic artery wall

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Abstract

Measurements of the dielectric properties of healthy and atherosclerotic human artery tissues were made in the frequency range of 100 Hz–100 kHz and temperatures from 22 to 260°C. The temperature dependencies of the dielectric parameters for healthy tissues reveal distinctively the temperature ranges corresponding to the release of water up to 200°C and the decomposition processes of elastin and collagen, above this temperature. The influence of atherosclerosis on the dielectric properties of artery tissues is significant in the whole temperature range. The relative permittivity for atherosclerotic tissues at the same temperature is much lower than for the healthy tissues. This suggests, that the polarization in atherosclerotic tissues due to protons hopping between a smaller number of sites than in healthy tissues, as a results of the thermal degradation of collagen–water. The data obtained above 200°C indicate that the atherosclerosis induces the higher physico-chemical changes in the collagen when compared to elastin.

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References

  1. Auerbach G, Gaill F, Jaenicke R, Schulthess T, Timpl R, Engel J (1994) Pressure dependence of collagen melting. Matrix Biol 14:589–592

    Article  Google Scholar 

  2. Blad B (1998) Impedance spectra of cancerous and normal tissues from a mouse. Bioelectrochem Bioenerg 45:169–172

    Article  Google Scholar 

  3. Brian G, Halloran MD, Valerie A et al (1995) Localization of aortic disease is associated with intrinsic differences in aortic structure. J Surg Res 59:17–22

    Article  Google Scholar 

  4. Buschman HP, Deinu G, Motz JT et al (2001) Raman microspectroscopy of human coronary atherosclerosis: biochemical assessment of cellular and extracellular morphologic structures in situ. Cardiovasc Pathol 10:69–82

    Article  Google Scholar 

  5. Jaroszyk F, Marzec E (1994) The effect of ionizing radiation on the dielectric properties of bovine Achilles tendon collagen in the temperature range of thermal denaturation. J Mater Sci 29:5353–5356

    Article  Google Scholar 

  6. Lee TC, Midura RJ, Hascall VC, Vesely I (2001) The effect of elastin damage on mechanics of the aortic valve. J Biomech 24:201–210

    Google Scholar 

  7. Lillie MA, Gosline JM (2002) The viscoelastic basis for the tensile strength of elastin. Int J Biol Macromol 30:119–127

    Article  Google Scholar 

  8. Manoharan R, Wang Y, Feld MS (1996) Histochemical analysis of biological tissues using Raman spectroscopy. Spectrochimica Acta Part A 52:215–249

    Article  Google Scholar 

  9. Marzec E (1998) A comparison of dielectric relaxation of bone and keratin. Bioelectrochem Bioenerg 46:29–32

    Article  Google Scholar 

  10. Marzec E, Wachal K (1999) The electrical properties of leg skin in normal individuals and in patients with ischemia. Bioelectrochem Bioenerg 49:73–75

    Article  Google Scholar 

  11. Marzec E, Warchoł W (2005) Dielectric properties of a protein–water system in selected animal tissues. Bioelectrochemistry 65:89–94

    Article  Google Scholar 

  12. Miyauchi T, Hirose H, Sasaki E et al (1999) Predictability of dielectric properties for ischemic injury of the skeletal muscle before reperfusion. J Surg Res 86:79–88

    Article  Google Scholar 

  13. Murata K, Motayama T, Kotake C (1986) Collagen types in various layers of the human aorta and their changes with the atherosclerotic process. Atherosclerosis 60:251–262

    Article  Google Scholar 

  14. Pezzin G, Scandola M, Gotte L (1976) The low-temperature mechanical relaxation of elastin. I. The dry protein. Biopolymers 15:283–292

    Article  Google Scholar 

  15. Pietrucha K, Marzec E (2005) Dielectric properties of the collagen–glycosaminogycans scaffolds in the temperature range of thermal decomposition. Biophys Chem 118:51–56

    Article  Google Scholar 

  16. Samouillan V, Lamure A, Maurel E, et at (2000) Characterization of elastin and collagen in aortic bioprostheses. Med Biol Eng Comput 38:226–231

    Article  Google Scholar 

  17. Schaefer M, Gross W, Ackemann J, Gebhard MM (2002) The complex dielectric spectrum of heart tissue during ischemia. Bioelectrochemistry 58:171–180

    Article  Google Scholar 

  18. Schmidt CE, Baier JM (2000) Acellular vascular tissues: natural biomaterials for tissue repair and tissue engineering. Biomaterials 21:2215–2231

    Article  Google Scholar 

  19. Weinberg PD, Winlove CP, Parker KH (1995) The distribution of water in arterial elastin: effects of mechanical stress, osmotic pressure, and temperature. Biopolymers 35:161–169

    Article  Google Scholar 

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Brzeziński, J., Oszkinis, G. & Marzec, E. Dielectric relaxation of a protein–water system in atherosclerotic artery wall. Med Bio Eng Comput 45, 525–529 (2007). https://doi.org/10.1007/s11517-007-0181-2

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  • DOI: https://doi.org/10.1007/s11517-007-0181-2

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