Structural Changes in Liver Histology in Common Kilka Clupeonella caspia Svetovidov, 1941 under Anthropogenic Pressure

封面

如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

详细

Histopathological changes are widely used as biomarkers of the health status of fish exposed to chemical compounds. Individuals of the common kilka Clupeonella caspia Svetovidov, 1941 caught from the Middle Caspian Sea exhibited significant changes in the cellular structure of the liver. The more common were signs of hyperemia: an edema of the liver parenchyma, vascular congestion, lympho-macrophage infiltration, small hemorrhages, and a narrowing of the bile duct lumen.

全文:

受限制的访问

作者简介

T. H. Nguyen

Astrakhan State Technical University

编辑信件的主要联系方式.
Email: hongvannguyen@mail.ru
ORCID iD: 0000-0002-6910-2705
俄罗斯联邦, Astrakhan

M. Grushko

Astrakhan State Technical University; Russian Biotechnological University

Email: hongvannguyen@mail.ru
ORCID iD: 0000-0001-7529-5382
俄罗斯联邦, Astrakhan; Moscow

N. Fedorova

Astrakhan State Technical University

Email: hongvannguyen@mail.ru
ORCID iD: 0000-0001-9411-6642
俄罗斯联邦, Astrakhan

V. Chaplygin

Astrakhan State Technical University

Email: hongvannguyen@mail.ru
ORCID iD: 0000-0002-0509-702X
俄罗斯联邦, Astrakhan

参考

  1. Волкова О.В., Елецкий Ю.К. Основы гистологии с гистологической техникой. М.: Медицина. 1989. С. 142–256.
  2. Гентен Ф., Тервинге Э., Данги А. Атлас гистологии рыб. СПб.: Проспект науки. 2016.
  3. Зайцев В.Ф. Биогеохимия Каспийского моря в условиях техногенеза биосферы // Биогеохимические инновации в условиях коррекции техногенеза биосферы: Тр. Международ. биогеохимичесого симпозиума (Тирасполь, 5–7 ноября 2020). 2020. Т. 1. С. 67–71.
  4. Мельникова М.С. Гистопатологические методы в оценке состояния здоровья рыб при искусственном выращивании // Проблемы патологии, иммунологии и охраны здоровья рыб и других гидробионтов: расширенные материалы IV Международ. конф. (Борок, 24–27 сентября 2015). Ярославль: Филигрань. 2015. С. 331–337.
  5. Неваленный А.Н., Ершова Т.С., Зайцев В.Ф., Чаплыгин В.А. Биогеохимический мониторинг содержания химических элементов Каспийского моря // Вестн. АГТУ. Сер.: Рыб. хоз-во. 2022а. № 4. С. 22–28.
  6. Неваленный А., Чаплыгин В., Федорова Н. Особенности изменений внутренних органов кефали-сингиля Liza aurata (Risso, 1910) // Вестн. АГТУ. Сер.: Рыб. хоз-во. 2022б. № 3. С. 60–65.
  7. Правдин И.Ф. Руководство по изучению рыб (преимущественно пресноводных). Москва: Пищ. пром-сть. 1966.
  8. Терпугова Н.Ю., Ван Н.Т.Х., Грушко М.П., Федорова Н.Н. Патоморфология печени и жабр у рыб дельты Волги // Вестн. Керченского гос. морского технол. ун-та. 2022. № 3. С. 39–49.
  9. Черепанова А.А., Дробот Г.П., Осипов В.В. и др. Гистохимическое исследование печени двух видов карасей из водоемов заповедника “Приволжская лесостепь” // Современные проблемы медицины и естественных наук. 2019. Вып. 8. C. 174–175.
  10. Abdel-Warith A.A., Younis E.M., Al-Asgah N.A., Wahbi O.M. Effect of zinc toxicity on liver histology of Nile tilapia, Oreochromis niloticus // Sci. Res. Essays. 2011. V. 6. № 17. P. 3760–3769.
  11. Agius C., Roberts R.J. Melano-macrophage centres and their role in fish pathology // J. Fish Dis. 2003. V. 26. № 9. P. 499–509. doi: 10.1046/j.1365-2761.2003.00485.x
  12. An atlas of fish histology: Normal and pathological feature / ed. T. Hibiya. Tokyo: Kodansha. 1982.
  13. Au D.W.T. The application of histo-cytopathological biomarkers in marine pollution monitoring: a review // Mar. Pollut. Bull. 2004. V. 48. № 9–10. P. 817–834.
  14. Bernet D., Schmidt H., Meier W. et al. Histopathology in fish: proposal for a protocol to assess aquatic pollution // J. Fish Dis. 1999. V. 22. № 1. P. 25–34.
  15. Boran H., Capkin E., Altinok I., Terzi E. Assessment of acute toxicity and histopathology of the fungicide captan in rainbow trout // Exp. Toxicol. Pathol. 2012. V. 64. № 3. P. 175–179.
  16. Couillard C.M., Hodson P.V. Pigmented macrophage aggregates: a toxic response in fish exposed to bleached-kraft mill effluent? // Environ. Toxicol. Chem. 1996. V. 15. P. 1844–1854.
  17. Dane H., Şişman T. Effects of heavy metal pollution on hepatosomatic ındex and vital organ histology in Alburnus mossulensis from Karasu River // Turk. J. Vet. Anim. Sci. 2020. V. 44. P. 607–617.
  18. 3906/vet-1904-50
  19. Gernhöfer M., Pawet M., Schramm M. et al. Ultrastructural biomarkers as tools to characterize the health status of fish in contaminated streams // J. Aquat. Ecosyst. Stress Recovery. 2001. V. 8. № 3–4. P. 241–260.
  20. Gomes I.B.S., Porto M.L., Santos M.C.L. et al. The protective effects of oral low-dose quercetin on diabetic nephropathy in hypercholesterolemic mice // Front. Physiol. 2015. V. 6. Art. ID 247.
  21. Haaparanta A., Valtonen E.T., Hoffmann R., Holmes J. Do macrophage centres in fresh water fishes reflect the differences in water quality? // Aquat. Toxic. 1996. V. 34. P. 253–272.
  22. Hadi A.A., Alwan S.F. Histopathological changes in gills, liver and kidney of fresh water fish, Tilapia zillii, exposed to aluminum // Int. J. Pharm. Life Sci. 2012. V. 3. № 11. P. 2071–2081.
  23. Hinton D.E., Laurén D.J. Liver structural alterations accompanying chronic toxicity in fishes: potential biomarkers of exposure // Biomarkers of environmental contamination. Boca Raton: Lewis Publ. 1993. Р. 51–65.
  24. Jalaludeen M.D., Arunachalam M., Raja M. et al. Histopathology of the gill, liver and kidney tissues of the freshwater fish Tilapia mossambica exposed to cadmium sulphate // Int. J. Adv. Biol. Res. 2012. V. 2. № 4. P. 572–578.
  25. Khan R.A., Barker D.E., Hooper R. et al. Histopathology in winter flounder (Pleuronectes americanus) living adjacent to a pulp and paper mill // Arch. Environ. Contam. Toxicol. 1994. V. 26. P. 95–102.
  26. López-López E., Sedeño-Díaz J.E. Biological indicators of water quality: The role of fish and macroinvertebrates as indicators of water quality // Environmental Indicators, Dordrecht: Springer. 2015. P. 643–661. doi: 10.1007/978-94-017-9499-2_37
  27. Lukin A., Sharova J., Belicheva L., Camus L. Assessment of fish health status in the Pechora River: effects of contamination // Ecotoxicol. Environ. Saf. 2011. V. 74. № 3. P. 355–365.
  28. Mackmull G., Michels N.A. Absorption of colloidal carbon from the peritoneal cavity in the teleost Tautogolabrus adspersus // Am. J. Anat. 1932. V. 51. P. 3–47.
  29. Manera M., Serra R., Isani G., Carpené E. Macrophage aggregates in gilthead sea bream fed copper, iron and zinc enriched diets // J. Fish Biol. 2000. V. 57. P. 457–465. doi: 10.1111/j.1095- 8649.2000.tb02184.x
  30. Manrique W.G., Claudiano G.S., Petrillo T.R. et al. Response of splenic melanomacrophage centers of Oreochromis niloticus (Linnaeus, 1758) to inflammatory stimuli by BCG and foreign bodies // J. Appl. Ichthyol. 2014. V. 30. № 5. P. 1001–1006.
  31. Murchelano R.A., Wolke R.E. Neoplasms and nonneoplastic liver lesions in winter flounder, Pseudopleuronectes americanus, from Boston Harbor, Massachusetts // Environ. Health Perspect. 1991. V 90. P. 17–26.
  32. Oliva M., Vicente-Martorell J.J., Galindo-Riano M.D., Perales J.A. Histopathological alterations in Senegal sole, Solea senegalensis, from a polluted Huelva estuary (SW, Spain) // Fish Physiol. Biochem. 2013. V. 39. № 3. P. 523–545.
  33. Oliveira L.A., Almeida J., Benini R., Crestani C.C. CRF1 and CRF2 receptors in the bed nucleus of the stria terminalis modulate the cardiovascular responses to acute restraint stress in rats // Pharmacol. Res. 2015. V. 95–96. P. 53–62. doi: 10.1016/j.phrs.2015.03.012
  34. Pintucci G., Manzionna M., Maida I. et al. Morpho-functional characterization of cultured pigment cells from Rana esculenta L. liver // In Vitro Cell Dev. Biol. 1990. V. 26. P. 659–664.
  35. Poleksic V., Lenhardt M., Jaric I. et al. Liver, gills, and skin histopathology and heavy metal content of the Danube sterlet (Acipenser ruthenus Linnaeus, 1758) // Environ. Toxicol. Chem. 2010. V. 29. № 3. P. 515–521. doi: 10.1002/etc.82
  36. Rabitto I.S., Costa J.R.M.A., Assis H.C.S. et al. Effects of dietary Pb(II) and tributyltin on neotropical fish, Hoplias malabaricus: histopathological and biochemical findings // Ecotoxicol. Environ. Saf. 2005. V. 60. № 2. P. 147–156.
  37. Rezende K.F.O., Santos R.M., Borges J.C.S. et al. Histopathological and genotoxic effects of pollution on Nile Tilapia (Oreochromis niloticus, Linnaeus, 1758) in the Billings Reservoir (Brazil) // Toxicol. Mech. Methods. 2014. V. 24. № 6. P. 404–411. doi: 10.3109/15376516.2014.925020
  38. Ribeiro H.J., Procópio M.S., Gomes J.M.M. et al. Functional dissimilarity of melanomacrophage centres in the liver and spleen from females of the teleost fish Prochilodus argenteus // Cell Tissue Res. 2011. V. 346. № 3. P. 417–425.
  39. Roberts R.J. Melanin-containing cells of teleost fish and their relation to disease // The pathology of fishes. Madison, Wis.: Univ. Wisconsin Press. 1975. P. 399–428.
  40. Scalia M., Geremia E., Corsaro C. et al. The extracutaneous pigmentary system: evidence for melanosynthesis in Amphibia and Reptilia liver // Comp. Biochem. Physiol. Part B: Comp. Biochem. 1988. V. 89. P. 715–717.
  41. Schmalz W.F.Jr., Hernandez A.D., Weis P. Hepatic histopathology in two populations of the mummichog, Fundulus heteroclitus // Mar. Environ. Res. 2002. V. 54. № 3–5. P. 539–542.
  42. Stentiford G.D., Longshaw M., Lyons B.P. et al. Histopathological biomarkers in estuarine fish species for the assessment of biological effects of contaminants // Mar. Environ. Res. 2003. V. 55. № 2. P. 137–159.
  43. Teh S.J., Adams S.M., Hinton D.E. Histopathological biomarkers in freshwater fish populations exposed to different types of contaminant stress // Aquat. Toxicol. 1997. V. 37. P. 51–70. doi: 10.1016/S0166-445X(96)00808-9
  44. Thophon S., Kruatrachue M., Upathan E.S. et al. Histopathological alterations of white seabass, Lates calcarifer, in acute and subchronic cadmium exposure // Environ. Pollut. 2003. V. 121. № 3. P. 307–320.
  45. Van Dyk J.C., Cochrane M.J., Wagenaar G.M. Liver histopathology of the sharptooth catfish Clarias gariepinus as a biomarker of aquatic pollution // Chemosphere. 2012. V. 87. № 4. P. 301–311.
  46. Wolf J.C., Wheeler J.R. A critical review of histopathological findings associated with endocrine and non-endocrine hepatic toxicity in fish models // Aquat. Toxicol. 2018. V. 197. P. 60–78. doi: 10.1016/j.aquatox.2018.01.013
  47. Wolke R.E. Piscine macrophage aggregates: a review // Annu. Rev. Fish Dis. 1992. V. 2. P. 91–108.
  48. Wolke R.E., Murchelano R.A., Dickstein C., George C.J. Preliminary evaluation of the use of macrophage aggregates (MA) as fish health monitors // Bull. Environ. Contamin. Toxicol. 1985. V. 35. P. 222–227.
  49. Xu W., Liu W., Lu K. et al. Effect of trichlorfon on oxidative stress and hepatocyte apoptosis of Carassius auratus gibelio in vivo // Fish Physiol. Biochem. 2012. V. 38. P. 769–775. https://doi.org/10.1007/s10695-011-9559-z
  50. Zuasti A., Jiménez-Cervantes C., García-Borón J.C., Ferrer C. The melanogenic system of Xenopus laevis // Arch. Histol. Cytol. 1998. V. 61. P. 305–316.
  51. Zurlo J., Rudacille D., Goldberg A.M. The three Rs: the way forward // Environ. Health Perspect. 1996. V. 104. P. 878–880.

补充文件

附件文件
动作
1. JATS XML
2. Fig. 1. Preserved liver structure of the common sprat Clupeonella caspia. Uv. ×1000. 1 – hepatocyte with a round nucleus, 2 – central vein, 3 – erythrocytes

下载 (669KB)
3. Fig. 2. Narrowed lumen of the bile duct in the liver of the common sprat Clupeonella caspia. Uv. ×400. 1 – separation of the basement membrane from cubic epithelial cells, 2 – narrowing of the lumen of the bile duct, 3 – a large granule of hemosiderin, 4 – an interlobular vein, 5 – shaped blood elements

下载 (714KB)
4. Fig. 3. Hepatocellular adenoma on the background of leukocyte infiltration in the liver of the common sprat Clupeonella caspia. Uv. ×400. 1 – a separate tumor site, 2 – edema of the liver parenchyma, 3 – vein

下载 (853KB)

版权所有 © The Russian Academy of Sciences, 2024