Evaluation of peripheral vasodilative indices in skin tissue of type 1 diabetic rats by use of RGB images

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• 作者：Noriyuki Tanaka ; Izumi Nishidate ; Kazuya Nakano ; Yoshihisa Aizu…
• 关键词：Arterial inflow ; Venous capacitance ; Skin hemodynamics ; RGB image ; Monte Carlo simulation ; Dorsal reversed McFarlane skin flap ; Type 1 diabetic rat
• 刊名：Optical Review
• 出版年：2016
• 出版时间：April 2016
• 年：2016
• 卷：23
• 期：2
• 页码：323-331
• 全文大小：2,078 KB
• 参考文献：1.Endemann, D.H., Schifferin, E.L.: Endothelial dysfunction. J. Am. Soc. Nephrol. 15, 1983–1992 (2004)CrossRef
  2.Hopman, M.T.E., Groothuis, J.T., Flendrie, M., Gerrits, K.H.L., Houtman, S.: Increased vascular resistance in paralyzed legs after spinal cord injury is reversible by training. J. Appl. Physiol. 93, 1966–1972 (2002)CrossRef
  3.Wecht, J.M., De Meersman, R.E., Weir, J.P., Bauman, W.A., Grimm, D.R.: Effects of autonomic disruption and inactivity on venous vascular function. Am. J. Physiol. Hear Circ. Physiol. 278, H515–H520 (2000)
  4.Eze, A.R., Cisek, P.L., Holland, B.S., Comerota, A.J., Verramasuneni, R., Comerota, A.J.: The contributions of arterial and venous volumes to increased cutaneous blood flow during leg compression. Ann. Vasc. Surg. 12, 182–186 (1998)CrossRef
  5.Rossi, M., Lall, K., Standfield, N., Dornhorst, A.: Impaired vasoconstriction of peripheral cutaneous blood flow in type 1 diabetic patients following food ingestion. Diabetic Med. 15, 463–466 (1998)CrossRef
  6.Kohner, E.M., Hamilton, A.M., Saunders, S.J., Sutcliffe, B.A., Bulpitt, C.J.: The retinal blood flow in diabetes. Diabetologia 11, 27–33 (1975)CrossRef
  7.Mogensen, C.E.: Glomerular filtration rate and renal plasma flow in short-term and long-term juvenile diabetes mellitus. Scand. J. Clin. Lab. Invest. 28, 91–100 (1971)CrossRef
  8.Parving, H.H., Viberti, G.C., Keen, H., Christiansen, J.S., Lassen, N.A.: Hemodynamic factors in the genesis of diabetic microangiopathy. Metabolism 32, 943–949 (1983)CrossRef
  9.Hewlett, A.W., van Zwaluwenburg, J.G.: The rate of blood flow in the arm. Heart 1, 87–97 (1909)
  10.Whitney, R.J.: The measurement of volume changes in human limbs. J. Physiol. 121, 1–27 (1953)CrossRef
  11.Lind, L., Sarabi, M., Millgard, J.: Methodological aspects of the evaluation of endothelium-dependent vasodilatation in the human forearm. Clin. Physiol. 18, 81–87 (1998)CrossRef
  12.Cooper, K.E., Edholm, O.G., Mottram, R.F.: The blood flow in skin and muscle of the human forearm. J. Physiol. 128, 258–267 (1955)CrossRef
  13.Hokanson, D.E., Sumner, D.S., Strandness, D.E.: An electrically calibrated plethysmograph for direct measurement of limb blood flow. IEEE Trans. Biomed. Eng. 22, 25–29 (1975)CrossRef
  14.Swampillai, J., Doshi, S., Fraser, A.G., Goodfellow, J., Jones, C.J.H.: Clinical assessment of endothelial function—an update. Br. J. Diabetes Vasc. Dis. 5, 72–76 (2005)CrossRef
  15.Panza, J.A., Quyyumi, A.A., Brush Jr, J.E., Epstein, S.E.: Abnormal endothelium-dependent vascular relaxation in patients with essential hypertension. N. Engl. J. Med. 323, 22–27 (1990)CrossRef
  16.Perticone, F., Ceravolo, R., Pujia, A., Ventura, G., Iacopino, S., Scozzafava, A., Ferraro, A., Chello, M., Mastroroberto, P., Verdecchia, P., Schillaci, G.: Prognostic significance of endothelial dysfunction in hypertensive patients. Circulation 104, 191–196 (2001)CrossRef
  17.Vigilance, J.E., Reid, H.L.: Venodynamic and hemorheological variables in patients with diabetes mellitus. Arch. Med. Res. 36, 490–495 (2005)CrossRef
  18.Newton, D.J., Khan, F., Belch, J.J.F.: Assessment of microvascular endothelial function in human skin. Clin. Sci. 101, 567–572 (2001)CrossRef
  19.Balmain, S., Padmanabhan, N., Ferrell, W.R., Morton, J.J., McMurray, J.J.V.: Differences in arterial compliance, microvascular function and venous capacitance between patients with heart failure and either preserved or reduced left ventricular systolic function. Eur. J. Heart Fail. 9, 865–871 (2007)CrossRef
  20.Dawson, J.B., Barker, D.J., Ellis, D.J., Grassam, E., Cotterill, J.A., Fisher, G.W., Feather, J.W.: A theoretical and experimental study of light absorption and scattering by in vivo skin. Phys. Med. Biol. 25, 695–709 (1980)CrossRef
  21.Feather, J.W., Saffar, M.H., Leslie, G., Dawson, J.B.: A portable scanning reflectance spectrophotometer using visible wavelengths for the rapid measurement of skin pigments. Phys. Med. Biol. 34, 807–820 (1989)CrossRef
  22.Harrison, D.K., Evans, S.D., Abbot, N.C., Beck, J.S., McCollum, P.T.: Spectrophotometric measurements of haemoglobin saturation and concentration in skin during the tuberculin reaction in normal human subjects. Clin. Phys. Physiol. Meas. 13, 349–363 (1992)CrossRef
  23.Newton, D.J., Harrison, D.K., Delaney, C.J., Beck, J.S., McCollum, P.T.: Comparison of macro- and micro-lightguide spectrophotometric measurements of microvascular haemoglobin oxygenation in the tuberculin reaction in normal human skin. Physiol. Meas. 15, 115–128 (1994)CrossRef
  24.Stratonnikov, A.A., Loschenov, V.B.: Evaluation of blood oxygen saturation in vivo from diffuse reflectance spectra. J. Biomed. Opt. 6, 457–467 (2001)ADS CrossRef
  25.Zonios, G., Bykowski, J., Kollias, N.: Skin melanin, hemoglobin, and light scattering properties can be quantitatively assessed in vivo using diffuse reflectance spectroscopy. J. Invest. Dermatol. 117, 1452–1457 (2001)CrossRef
  26.Stamatas, G.N., Kollias, N.: Blood stasis contributions to the perception of skin pigmentation. J. Biomed. Opt. 9, 315–322 (2004)ADS CrossRef
  27.Nishidate, I., Aizu, Y., Mishina, H.: Estimation of melanin and hemoglobin in skin tissue using multiple regression analysis aided by Monte Carlo simulation. J. Biomed. Opt. 9, 700–710 (2004)ADS CrossRef
  28.Bargo, P.R., Prahl, S.A., Goodell, T.T., Sleven, R.A., Koval, G., Blair, G., Jacques, S.L.: In vivo determination of optical properties of normal and tumor tissue with white light reflectance and empirical light transport model during endoscopy. J. Biomed. Opt. 10, 034018-1–034018-15 (2005)ADS CrossRef
  29.Tseng, S.-H., Bargo, P., Durkin, A., Kollias, N.: Chromophore concentrations, absorption and scattering properties of human skin in vivo. Opt. Exp. 17, 14600–14617 (2009)ADS
  30.Sowa, M.G., Payette, J.R., Hewko, M.D., Mantsch, H.H.: Visible-near infrared multispectral imaging of the rat dorsal skin flap. J. Biomed. Opt. 4, 474–481 (1999)ADS CrossRef
  31.Dunn, A.K., Devor, A., Bolay, H., Andermann, M.L., Moskowitz, M.A., Dale, A.M., Boas, D.A.: Simultaneous imaging of total cerebral hemoglobin concentration, oxygenation, and blood flow during functional activation. Opt. Lett. 28, 28–30 (2003)ADS CrossRef
  32.Vogel, A., Chernomordik, V.V., Riley, J.D., Hassan, M., Amyot, F., Dasgeb, B., Demos, S.G., Pursley, R., Little, R.F., Yarchoan, R., Tao, Y., Gandjbakhche, A.H.: Using noninvasive multispectral imaging to quantitatively assess tissue vasculature. J. Biomed. Opt. 12, 051604-1–051604-13 (2007)ADS CrossRef
  33.Tsumura, N., Haneishi, H., Miyake, Y.: Independent-component analysis of skin color image. J. Opt. Soc. Am. A 16, 2169–2176 (1999)ADS CrossRef
  34.O’Doherty, J., Henricson, J., Anderson, C., Leahy, M.J., Nilsson, G.E., Sjöberg, F.: Sub-epidermal imaging using polarized light spectroscopy for assessment of skin microcirculation. Skin Res. Technol. 13, 472–484 (2007)CrossRef
  35.O’Doherty, J., McNamara, P., Clancy, N.T., Enfield, J.G., Leahy, M.J.: Comparison of instrument for investigation of microcirculatory blood flow and red blood cell concentration. J. Biomed. Opt. 14, 034025 (2009)CrossRef
  36.Nishidate, I., Tanaka, N., Kawase, T., Maeda, T., Yuasa, T., Aizu, Y., Yuasa, T., Niizeki, K.: Noninvasive imaging of human skin hemodynamics using a digital red-green-blue camera. J. Biomed. Opt. 16, 086012 (2011)ADS CrossRef
  37.Nishidate, I., Tanaka, N., Kawase, T., Maeda, T., Yuasa, T., Aizu, Y., Yuasa, T., Niizeki, K.: Visualization of peripheral vasodilative indices in human skin by use of red, green, blue images. J. Biomed. Opt. 18, 061220 (2013)ADS CrossRef
  38.Wang, L.-H., Jacques, S.L., Zheng, L.-Q.: MCML-Monte Carlo modeling of photon transport in multi-layered tissues. Comput. Methods Programs Biomed. 47, 131–146 (1995)CrossRef
  39.Jacques, S.L., Glickman, R.D., Schwartz, J.A.: Internal absorption coefficient and threshold for pulsed laser disruption of melanosomes isolated from retinal pigment epithelium. Proc. SPIE 2681, 468–477 (1996)ADS CrossRef
  40.Prahl, S.A.: Tabulated Molar Extinction Coefficient for Hemoglobin in Water. http://​omlc.​ogi.​edu/​spectra/​hemoglobin/​summary.​html (1999)
  41.Jacques, S.L.: Origins of tissue optical properties in the UVA, visible, and NIR region. In: Alfano, R.R., Fujimoto, J.G. (eds.) OSA TOPS on Advances in Optical Imaging and Photon Migration, vol. 2, pp. 364–369. Optical Society of America, Washington (1996)
  42.van Gemert, M.J.C., Jacques, S.L., Sterenborg, H.J.C.M., Star, W.M.: Skin optics. IEEE Trans. Biomed. Eng. 36, 1146–1154 (1989)CrossRef
  43.Groothuis, J.T., van Vliet, L., Kooijman, M., Hopman, M.T.E.: Venous cuff pressures from 30 mmHg to diastolic pressure are recommended to measure arterial inflow by plethysmography. J. Appl. Physiol. 95, 342–347 (2003)CrossRef
  44.Schreuder, M.F., Fodor, M., van Wijk, J.A.E., Delemarre-van de Waal, H.A.: Weekend versus working day: differences in telemetric blood pressure in male Wistar rats. Lab. Anim. 41, 86–91 (2007)CrossRef
  45.Chapman, J.T., Hreash, F., Laycock, J.F., Walter, S.J.: The cardiovascular effects of vasopressin after haemorrhage in anaesthetized rats. J. Physiol. 375, 421–434 (1986)CrossRef
  46.Terata, K., Coppey, L.J., Davidson, E.P., Dunlap, J.A., Gutterman, D.D., Yorek, M.A.: Acetylcholine-induced arteriolar dilation is reduced in streptozotocin-induced diabetic rats with motor nerve dysfunction. Br. J. Pharmacol. 128, 837–843 (1999)CrossRef
  47.Mahmud, F.H., Van Uum, S., Kanji, N., Thiessen-Philbrook, H., Clarson, C.L.: Impaired endothelial function in adolescents with type 1 diabetes mellitus. J. Pediatr. 152, 557–562 (2007)CrossRef
  48.Haller, M.J., Stein, J., Shuster, J., Theriaque, D., Silverstein, J., Schatz, D.A., Earing, M.G., Lerman, A., Mahmud, F.H.: Peripheral artery tonometry demonstrates altered endothelial function in children with type 1 diabetes. Pediatr. Diabetes 8, 193–198 (2007)CrossRef
  49.Chittenden, S.J., Shami, S.K.: Microvascular investigations in diabetes mellitus. Postgrad. Med. J. 69, 419–428 (1993)CrossRef
  
• 作者单位：Noriyuki Tanaka (1)
  Izumi Nishidate (1)
  Kazuya Nakano (2)
  Yoshihisa Aizu (3)
  Kyuichi Niizeki (4)
  
  1. Graduate School of Bio-application and Systems Engineering, Tokyo University of Agriculture and Technology, Koganei, Tokyo, 184-8588, Japan
  2. Faculty of Science, Division II, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku, Tokyo, 162-8601, Japan
  3. Graduate School of Mechanical Systems and Materials Engineering, Muroran Institute of Technology, Muroran, Hokkaido, 050-8588, Japan
  4. Graduate School of Biosystem Engineering, Yamagata University, Yonezawa, Yamagata, 992-8510, Japan
  
• 刊物类别：Physics and Astronomy
• 刊物主题：Physics
  Electromagnetism, Optics and Lasers
  
• 出版者：The Optical Society of Japan, co-published with Springer-Verlag GmbH
• ISSN：1349-9432

文摘

We investigated a method to evaluate the arterial inflow and the venous capacitance in the skin tissue of streptozotocin-induced type 1 diabetic rats from RGB digital color images. The arterial inflow and the venous capacitance in the dorsal reversed McFarlane skin flap are calculated based on the responses of change in the total blood concentration to occlusion of blood flow to and from the flap tissues at a pressure of 50 mmHg. The arterial inflow and the venous capacitance in the skin flap tissue were significantly reduced in type 1 diabetic rat group compared with the non-diabetic rat group. The results of the present study indicate the possibility of using the proposed method for evaluating the peripheral vascular dysfunctions in diabetes mellitus.