Age-related features of the organization of the microcirculatory bed of the bulbar conjunctiva
https://doi.org/10.34215/1609-1175-2020-3-57-61
Abstract
Objective: Analysis of age-related changes of microcirculatory bed of bulbar conjunctiva.
Methods: 46 individuals of both sexes, divided into 5 age groups according to WHO recommendations, were examined. Biomicroscopy of bulbar conjunctiva was performed using a non-mydriatic retinal camera TOPCON TRC-NW8F (Japan); the obtained images were processed with a mea‑ suring device of automated analysis system ImageScope (Leica, Germany).
Results: The average diameter of arterioles, arterioleto-venule ratio (AVR) and specific density of capillaries were the largest, and the diameter of venules was the smallest among the subjects aged 18–44 years. The most sensitive indicators of the state of microcirculatory bed were AVR and the specific density of capillaries, the values of which in the group of 45–59-year-olds were 10–11% lower than in people aged 18–24 and 25–44 years. Differences in other indicators between people aged 18-24 and 45–59 years were not significant. Between the groups of 60–74 and 75–86-year-old participants of the study, pronounced differences (about 18%) were found only in the specific density of capillaries: compared with 18–24 and 45–59-year-olds, this indicator decreased by almost 1.5 times, AVR – only by a third, and changes in the average diameter of arterioles and venules did not exceed 9–12%. Elderly people more often demonstrated arteriolar spasm, their uneven caliber, avascular fields and other disorders of the structure of the micro‑ circulatory bed.
Conclusions: As the body ages, in the microcirculatory bed of the bulbar conjunctiva, the number of atypical vascular formations increases, the diameter of the arterioles decreases, the AVR and the specific density of capillaries decrease, the diameter of the venules increases.
About the Authors
V. M. ChertokRussian Federation
MD, PhD, professor, head of the Department of Human Anatomy,
2, Ostryakova Ave., Vladivostok, 690002
V. A. Nevzorova
Russian Federation
MD, PhD, professor, head of the Institute of Intrinic Medicine and Instrumental diagnostics,
2, Ostryakova Ave., Vladivostok, 690002
A. K. Savchenko
Russian Federation
student,
2, Ostryakova Ave., Vladivostok, 690002
O. V. Miroshnichenko
Russian Federation
MD, PhD,
10 Ajax Bay, Russky Island, Vladivostok, 690922
A. V. Laryushkina
Russian Federation
MD, PhD, associate professor,
2, Ostryakova Ave., Vladivostok, 690002
References
1. Kozlov VI. Capillarosсopy in clinical practice. Moscow: Prakticheskaya Medicina; 2015:232 (In Russ).
2. Bogoyavlenskaya OV, Oslopov VN. Study of the state of the microcirculation system in arterial hypertension. Practical Medicine. 2010;5(44):116–8 (In Russ).
3. Safonova TN, Lutsevich EE, Kintukhina NP. Microcirculatory changes in bulbar conjunctiva in various diseases. The Russian Annals of Ophthalmology. 2016;132(2):90–5 (In Russ).
4. Chertok VM, Chertok AG. Regulatory capacity of the brain capillaries. Pacific Medical Journal. 2016;2:72–81 (In Russ).]
5. Chertok VM, Kotsyuba AE. Age-associated characteristics of vasomotor regulation of the pia mater arteries in rats. Bull Exp Biol Med. 2010;149(3):364–8.
6. Vereshchaka VV. Features of eye microcirculation in healthy people of different ages. Fiziol Zh. 2007;53(6):60–6.
7. Kotsyuba AE, Chertok VM, Chertok AG. Age-specific characteristics of CO-mediated reaction of the pial arteries of various diameters in rats. Bull Exp Biol Med. 2017;162(5):658–63.
8. Fedorovich AA. The functional state of regulatory mechanisms of the microcirculatory blood flow in normal conditions and in arterial hypertension according to laser Doppler flowmetry. Regional Blood Circulation and Microcirculation. 2010;1:49–60 (In Russ).
9. Kuleva NV, Fedorov DA, Krasovskaya IE. The role of different ways of nitrite oxide generation in mammalian blood vessels in aging. Cytology. 2018;60(1):5–13 (In Russ).
10. Seal DR, Jablonski RL, Donato AJ. Aging and vascular endothelial function in human. Clin Sci (London). 2011;120:357–75.
11. Donato AJ, Morgan RG, Walker AE, Lesniewski LA. Cellular and molecular biology of aging endothelial cells. J Mol Cell Cardiol. 2015;89(Pt B):122–35.
12. El Assar M, Angulo J, Rodríguez-Mañas L. Oxidative stress and vascular inflammation in aging. Free Radic Biol Med. 2013;65:380–401.
13. Lassegue B, Griendling KK. NADPH oxidases: function and pathologies in the vasculature. Arterioscler Tromb Vasc Biol. 2010;30:653–61.
14. Wenzel P, Schuhmacher S, Kienhofer J, Muller J, Hortmamm M, Octze M, et al. Manganese superoxide dismutase and aldehyde dehydrogenase deficiency increase mitochondrial oxidative stress and aggravate age-dependent vascular dysfunction. Cardiovasc Res. 2008;80:280–9.
15. Hong F, Larrea MD, Doughty C, Kwiatkowski DJ, Squillace R, Slingerland JM. mTOR-raptor binds and activates SGK1 to regulate p27 phosphorylation. Mol Cell. 2008;30(6):701–11.
Review
For citations:
Chertok V.M., Nevzorova V.A., Savchenko A.K., Miroshnichenko O.V., Laryushkina A.V. Age-related features of the organization of the microcirculatory bed of the bulbar conjunctiva. Pacific Medical Journal. 2020;(3):57-61. (In Russ.) https://doi.org/10.34215/1609-1175-2020-3-57-61