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Morphofunctional Characteristic of the Greater Omentum

https://doi.org/10.18499/2225-7357-2020-9-2-90-99

Abstract

The paper provides a brief data overview of the national and the foreign recent decades literature on various aspects of the morphofunctional organization of the greater omentum in the physiological and various pathological states of the organism (in the process of morphogenesis, in the conditions of age-related alterations, under various experimental exposures, as well as in the postoperative transformations after surgical interventions due to inflammatory and tumor processes). The data on morphofunctional organization of the greater omentum main tissue components (mesothelium, adipose and lymphoid tissues) have been analyzed and summarized.

About the Authors

N. N. Shevlyuk
Orenburg State Medical University
Russian Federation

ul. Sovetskaya, 6, Orenburg, 460000, Russian Federation



L. V. Khalikova
Bashkir State Medical University
Russian Federation
Ufa


A. A. Khalikov
Bashkir State Medical University
Russian Federation
Ufa


References

1. Berezovskaya SE. Strukturnaya organizatsiya bol'shogo sal'nika kak immunokompetentnogo organa (eksperimental'no-morfologicheskoe issledovanie): avtoref. diss. … kand. med. nauk. Yaroslavl'; 1990 (in Russian).

2. Berezovskaya SE, Markov II. Funktsional'noe znachenie bol'shogo sal'nika kak immunokompetentnogo organa. Fiziologiya vegetativnoi nervnoi sistemy. Kuibyshev: KMI; 1988: 17–8 (in Russian).

3. Bol'shoi sal'nik. Pod red. D LibermanMerffert, Kh. Uait. Per. s angl. Moscow: Meditsina; 1989 (in Russian).

4. Velichaskaya AG, Yermolin IL, Pogadayeva YeV, Bugrova ML. Structural changes of omentum adipose tissue in diastasis of the damaged sciatic nerve. Morfologiia. 2018;153(3):57–8 (in Russian).

5. Gataullin NG, Gantsev ShKh, Khunafin SN. Diagnostika i lechenie zabolevanii bol'shogo sal'nika. Ufa: Bashkirskoe kn. izd-vo; 1988 (in Russian).

6. Dedov II, Mel'nichenko GA, Butrova SA. Zhirovaya tkan' kak endokrinnyi organ. Obesity and Metabolism. 2006;1:6–13 (in Russian).

7. Doroshkevich SV, Doroshkevich EYu. Porazhenie zhirovoi tkani pri eksperimental'nom pankreatite. Morfologiia. 2009;136(4):52 (in Russian).

8. Zurnadzhan SA, Musatov OV, Trizno MN, Fomichev VV. Microcirculation parameters of the anterior abdominal wall tissues and some abdominal organs in rabbits. Morfologiia. 2018;153(3):117 (in Russian).

9. Zurnadzhan SA, Musatov OV, Chernukhin AA, Khairulin YuKh. Izmenenie soderzhaniya tkanevogo IgG posle gastro- i omentolienoplastiki v eksperimente. The Scientific Notes of the Pavlov University. 2006;13(4):73–5 (in Russian).

10. Ivanova VF. Interrelation of nuclear envelope with cell organelles in peritoneal cells during ontogenesist and in experimental pathology. Morfologiia. 2013;143(2):51–7 (in Russian).

11. Ivanova VF. Epitelii seroznykh obolochek. V kn.: Rukovodstvo po gistologii. 2-e izdanie, ispravl. i dopoln. Pod red RK Danilova. Saint-Petersburg: SpetsLit; 2011 (in Russian).

12. Karaganov YaL, Mironov VA, Gusev SA. O fiziologicheskom znachenii i mekhanizmakh obrazovaniya «stomat» v mezotelii bryushiny. Arkhiv anatomii. 1981;80(4):85–94 (in Russian).

13. КKolesnikov LL, Parkhomenko YuG, Sabirov ShR, Chukbar AV, Tishkevich OA. Morfologicheskii analiz razlichnykh vidov gemostaza nekotorykh parenkhimatoznykh organov. Morfologiia. 2006;129(4):66 (in Russian).

14. Lomakin VI, Vostrilov IM, Pelikh KI, Karelina NR. Stroenie i krovosnabzhenie bol'shogo sal'nika. Morfologiia. 2012;141(3):93–4 (in Russian).

15. Makurina O.N., Shalaev S.V., Shatskova I.A. Vliyanie immunogennykh vozdeistvii na morfofunktsional'noe sostoyanie bol'shogo sal'nika nekotorykh vidov mlekopitayushchikh. Rossiiskie morfologicheskie vedomosti. 2001;1–2:35 (in Russian).

16. Maslova NA, Ovchinnikova TV. Spatial orientation of precapillary arterioles in human lesser omentum. Morfologiia. 2018;153(3):180 (in Russian).

17. Maslova NA, Ovchinnikova TN. Organizatsiya zhirovoi tkani v malom sal'nike. Morfologiia. 2009;136(4):96 (in Russian).

18. Musatov OV, Zurnadjan SA,Trizno MN. The dynamics of microcirculation in the gastric flap and the epiploon after autoplasty by them of spleen wound in experiment. Astrakhan Medical Journal. 2012;7(4):190–3 (in Russian).

19. Musatov OV, Zurnadjan SA, Hirulin YuH. comparative morphologic and immunomorphologic estimation of reparative process after gastro- and omentumnephroplastics in the experiment. Astrakhan Medical Journal. 2011;6(1):87–91 (in Russian).

20. Nekrutov AV, Karasiova OV, Roshal LM. Greater omentum: morphofunctional characteristics and clinical significance in pediatrics. Voprosy Sovremennoi Pediatrii. 2007;6:58–63 (in Russian).

21. Novikova EG, Shevchuk AS, Pronin SM. Rezektsiya bol'shogo sal'nika u bol'nykh so zlokachestvennymi opukholyami yaichnikov. Rossiyskiy vestnik akushera-ginekologa. 2005;4:36–40 (in Russian).

22. Stranzha NB, Banin VV, Suslov VB, Likhacheva LM, et al. Cytological reactions during the formation of an artificial abdominal wall using a Parietex polymer network. Morfologiia. 2012;141(3):151 (in Russian).

23. Khalikova LV. Greater omentum: morphofunctional characteristics and clinical significans in oncology. Creative surgery and oncology. 2011;4:131–4 (in Russian).

24. Attard J-AP., MacLean AR. Adhesive small bowel obstruction: epidemiology, biology and prevention. Can J Surg. 2007;50(4):291–300.

25. Brüggmann D, Tchartchian G, Wallwiener M, Münstedt K, Tinneberg H-R, Hackethal A. Intraabdominal Adhesions. Deutsches Aerzteblatt Online. 2010 Nov 5;107:769–75. doi: 10.3238/arztebl.2010.0769

26. Chen J-Y, Chiu J-H, Chen H-L, Chen T-W, Yang W-C, Yang A-H. Human Peritoneal Mesothelial Cells Produce Nitric Oxide: Induction by Cytokines. Peritoneal Dialysis International: Journal of the International Society for Peritoneal Dialysis. 2000 Nov;20(6):772–7. doi: 10.1177/089686080002000631

27. Cheong YC, Laird SM, Li TC, Shelton JB, Ledger WL, Cooce ID. Peritoneal healing and adhesion formation/reformation. Human Reproduction Update. 2001 Nov 1;7(6):556–66. doi: 10.1093/humupd/7.6.556

28. Cheong YC, Laird SM, Shelton JB, Ledger WL, Li TC, Cooce ID. The correlation of adhesions and peritoneal fluid cytokine concentrations: a pilot study. Human Reproduction. 2002 Apr 1;17(4):1039–45. doi: 10.1093/humrep/17.4.1039

29. Cronauer MV, Stadlmann S, Klocker H, Abendstein B, Eder IE, Rogatsch H, et al. Basic Fibroblast Growth Factor Synthesis by Human Peritoneal Mesothelial Cells. The American Journal of Pathology. 1999 Dec;155(6):1977–84. doi: 10.1016/s0002-9440(10)65516-2

30. Darimont C, Avanti O, Blancher F, Wagniere S, Mansourian R, Zbinden I, et al. Contribution of mesothelial cells in the expression of inflammatory-related factors in omental adipose tissue of obese subjects. International Journal of Obesity. 2007 Jul 17;32(1):112–20. doi: 10.1038/sj.ijo.0803688

31. Durgakeri PU, Kaska M. Post-operative intraperitoneal adhesion prevention – the recent knowledge. Rozhl Chir. 2006 Jun;85(6):286-9.

32. Fedorko ME, Hirsch JG. Studies on transport of macromolecules and small particles across mesothelial cells of the mouse omentum. Experimental Cell Research. 1971 Nov;69(1):113–27. doi: 10.1016/0014-4827(71)90317-x

33. Foley-Comer AJ, Herrick SE, Al-Mishlab T, et al. Evidence for incorporation of free-floating mesothelial cells as a mechanism of serosal healing. J Cell Sci. 2002 Apr 1;115(7):1383-9.

34. Fotev Z, Whitaker D, Papadimitriou JM. Role of macrophages in mesothelial healing. The Journal of Pathology. 1987 Mar;151(3):209–19. doi: 10.1002/path.1711510309

35. Ghellal AM, Syucchi A.F, Chegini N, et al. Role of transforming growth factor beta-1 in peritonitisinduced adhesions,. Journal of Gastrointestinal Surgery. 2000 Jun;4(3):316–23.

36. Grant HW, Parker MC, Wilson MS, Menzies D, Sunderland G, Thompson JN, et al. Populationbased analysis of the risk of adhesion-related readmissions after abdominal surgery in children. Journal of Pediatric Surgery. 2006 Aug;41(8):1453–6. doi: 10.1016/j.jpedsurg.2006.04.023

37. Grant HW, Parker MC, Wilson MS, Menzies D, Sunderland G, Thompson JN, et al. Adhesions after abdominal surgery in children. Journal of Pediatric Surgery. 2008 Jan;43(1):152–7. doi: 10.1016/j.jpedsurg.2007.09.038

38. Havel PJ. Update on Adipocyte Hormones: Regulation of Energy Balance and Carbohydrate/Lipid Metabolism. Diabetes. 2004 Jan 28;53(1):S143–51. doi: 10.2337/diabetes.53.2007.s143

39. Healy JC, Reznek RH. The peritoneum, mesenteries and omenta: normal anatomy and pathological processes. European Radiology. 1998 Jul 28;8(6):886–900. doi: 10.1007/s003300050485

40. Hobson KG. Expression of Transforming Growth Factor β1 in Patients With and Without Previous Abdominal Surgery. Archives of Surgery. 2003 Nov 1;138(11):1249–52. doi: 10.1001/archsurg.138.11.1249

41. Horowitz NS, Miller A, Rungruang B, Richard SD, Rodriguez N, Bookman MA, et al. Does Aggressive Surgery Improve Outcomes? Interaction Between Preoperative Disease Burden and Complex Surgery in Patients With AdvancedStage Ovarian Cancer: An Analysis of GOG 182. Journal of Clinical Oncology. 2015 Mar 10;33(8):937–43. doi: 10.1200/jco.2014.56.3106

42. Kamel RM. Prevention of postoperative peritoneal adhesions. European Journal of Obstetrics & Gynecology and Reproductive Biology. 2010 Jun;150(2):111–8. doi: 10.1016/j.ejogrb.2010.02.003

43. Kasahara M, Yamaguchi H, Kageyama K. Studies on the antibody formation of the cultured omentum cells using hemolytic plaque method. Pathology International. 1973 Feb;23(1):43–9. doi: 10.1111/j.1440-1827.1973.tb00773.x

44. Kawanishi K. Diverse properties of the mesothelial cells in health and disease. Pleura and Peritoneum. 2016 Jun 1;1(2):79–89. doi: 10.1515/pp-2016-0009

45. Kim S, Moustaid-Moussa N. Secretory, Endocrine and Autocrine/Paracrine Function of the Adipocyte. The Journal of Nutrition. 2000 Dec 1;130(12):3110S-3115S. doi: 10.1093/jn/130.12.3110s

46. Kimber CP, Westmore P, Hutson JM, Kelly J. Primary omental torsion in children. Journal of Paediatrics and Child Health. 1996 Feb;32(1):22–4. doi: 10.1111/j.1440-1754.1996.tb01535.x

47. Krist LFG, Eestermans IL, Steenbergen JJE, Hoefsmit ECM, Cuesta MA, Meyer S, et al. Cellular composition of milky spots in the human greater omentum: An immunochemical and ultrastructural study. The Anatomical Record. 1995 Feb;241(2):163–74. doi: 10.1002/ar.1092410204

48. Kurman RJ, Shih I-M. The Dualistic Model of Ovarian Carcinogenesis. The American Journal of Pathology. 2016 Apr;186(4):733–47. doi: 10.1016/j.ajpath.2015.11.011

49. Lambert FG. Milky spots in the greater omentum. Cancer Immunol. Immunother. 1998;47:20–12.

50. Lanfrancone L, Boraschi D, Ghiara P, Falini B, Grignani F, Peri G, et al. Human peritoneal mesothelial cells produce many cytokines (granulocyte colony-stimulating factor [CSF], granulocyte-monocyte-CSF, macrophage- CSF, interleukin-1 [IL-1], and IL-6) and are activated and stimulated to grow by IL-1. Blood. 1992 Dec 1;80(11):2835–42. doi: 10.1182/blood.v80.11.2835.bloodjournal80112835

51. Liakakos T, Thomakos N, Fine PM, Dervenis C, Young RL. Peritoneal Adhesions: Etiology, Pathophysiology, and Clinical Significance. Digestive Surgery. 2001;18(4):260–73. doi: 10.1159/000050149

52. LI S, LI Q. Cancer stem cells and tumor metastasis. International Journal of Oncology. 2014 Apr 2;44(6):1806–12. doi: 10.3892/ijo.2014.2362

53. Li M-Z, Lian L, Xiao L, Wu W, He Y, Song X. Laparoscopic versus open adhesiolysis in patients with adhesive small bowel obstruction: a systematic review and meta-analysis. The American Journal of Surgery. 2012 Nov;204(5):779–86. doi: 10.1016/j.amjsurg.2012.03.005

54. Madison LD, Bergstrom-Porter B, Torres AR, Shelton E. Regulation of surface topography of mouse peritoneal cells. Formation of microvilli and vesiculated pits on omental mesothelial cells by serum and other proteins. The Journal of Cell Biology. 1979 Sep 1;82(3):783–97. doi: 10.1083/jcb.82.3.783

55. Miura M, Yonemura Y. Morphological study of human omental milky spots and their morphological changes in omental disseminated metastasis. Jap. J. Lymphology. 2011;34:2–6.

56. Mogensen JB, Kjær SK, Mellemkjær L, Jensen A. Endometriosis and risks for ovarian, endometrial and breast cancers: A nationwide cohort study. Gynecologic Oncology. 2016 Oct;143(1):87–92. doi: 10.1016/j.ygyno.2016.07.095

57. Mutsaers SE, Whitaker D, Papadimitriou JM. Mesothelial regeneration is not dependent on subserosal cells. The Journal of Pathology. 2000 Jan;190(1):86–92. doi: 10.1002/(sici)1096-9896(200001)190

58. Mutsaers SE. Mesothelial cells: Their structure, function and role in serosal repair. Respirology. 2002 Sep;7(3):171–91. doi: 10.1046/j.1440-1843.2002.00404.x

59. Mutsaers SE. The mesothelial cell. The International Journal of Biochemistry & Cell Biology. 2004 Jan;36(1):9–16. doi: 10.1016/s1357-2725(03)00242-5

60. Nehéz L, Vödrös D, Axelsson J, Tingstedt B, Lindman B, Andersson R. Prevention of postoperative peritoneal adhesions: Effects of lysozyme, polylysine and polyglutamate versus hyaluronic acid. Scandinavian Journal of Gastroenterology. 2005 Jan;40(9):1118–23. doi: 10.1080/00365520510023332

61. Ohtani O, Ohtani Y. Organization and developmental aspects of lymphatic vessels. Archives of Histology and Cytology. 2008;71(1):1–22. doi: 10.1679/aohc.71.1

62. Ott D. Laparoscopy and Adhesion Formation, Adhesions and Laparoscopy. Seminars in Reproductive Medicine. 2008 Jul;26(04):322–30. doi: 10.1055/s-0028-1082390

63. Park SL, Caberto CP, Lin Y, Goodloe RJ, Dumitrescu L, Love S-A, et al. Association of Cancer Susceptibility Variants with Risk of Multiple Primary Cancers: The Population Architecture using Genomics and Epidemiology Study. Cancer Epidemiology Biomarkers & Prevention. 2014 Aug 19;23(11):2568–78. doi: 10.1158/1055-9965.epi-14-0129

64. Pezzolla FG, Maiorino R, Ferrarese F. Peritoneal adhesions: pathophysiology. G Chir. 2008;29(3):115–25.

65. Podgrabinska S, Skobe M. Role of lymphatic vasculature in regional and distant metastases. Microvascular Research. 2014 Sep;95:46–52. doi: 10.1016/j.mvr.2014.07.004

66. Rasouli N, Kern PA. Adipocytokines and the Metabolic Complications of Obesity. The Journal of Clinical Endocrinology & Metabolism. 2008 Nov 1;93(1):64–73.. doi: 10.1210/jc.2008-1613

67. Saed GM, Zhang W, Chegini N, Holmdahl L, Diamond MP. Transforming Growth Factor Beta Isoforms Production by Human Peritoneal Mesothelial Cells after Exposure to Hypoxia. American Journal of Reproductive Immunology. 2000 May;43(5):285–91.. doi: 10.1111/j.8755-8920.2000.430507.x

68. Senthilkumar MP, Dreyer JS. Peritoneal adhesions: pathogenesis, assessment and effects. Trop. Gastroenterol. 2006;27(1):11–8.

69. Shavell VI, Saed GM, Diamond MP. Review: Cellular Metabolism: Contribution to

70. Postoperative Adhesion Development. Reproductive Sciences. 2009 Mar 16;16(7):627–34. doi: 10.1177/1933719109332826

71. Shimotsuma M, Kawata M, Hagiwara A, Takahashi T. Milky Spots in the Human Greater Omentum. Cells Tissues Organs. 1989;136(3):211–6. doi: 10.1159/000146888

72. Shimotsuma M, Simpson-Morgan MW, Takahashi T, Hagiwara A. Activation of omental milky spot macrophages by intraperitoneal administration of a streptococcal preparation, OK-432. Cancer Res. 1992;52(19):5400–2.

73. Schoppmann SF. Limphangiogenesis, inflammation and metastasis. Anticancer Res. 2005;25:4503–11.

74. Thompson J. Pathogenesis and prevention of adhesion formation. Digestive Surgery.1998;15(2):1054–57. doi: 10.1159/000018610

75. Torre M, Favre A, Pini Prato A, Brizzolara A, Martucciello G. Histologic study of peritoneal adhesions in children and in a rat model. Pediatric Surgery International. 2002 Dec;18(8):673–6. doi: 10.1007/s00383-002-0872-6

76. Vodice A. The greater omentum a uselles and hazardous organ for the patient and surgeon. Advantages of omentectomie in all abdominal operations. Dia. Med. Dia Med. 1963 Jan 28;35:69–70.

77. Wang Y, Oliver G. Current views on the function of the lymphatic vasculature in health and disease. Genes & Development. 2010 Oct 1;24(19):2115–26. doi: 10.1101/gad.1955910

78. Yao V, Platell C, Hall JC. Role of peritoneal mesothelial cells in peritonitis. British Journal of Surgery. 2003;90(10):1187–94. doi: 10.1002/bjs.4373

79. Yao V, Platell C, Hall JC. Peritoneal mesothelial cells produce inflammatory related cytokines. ANZ Journal of Surgery. 2004 Nov;74(11):997–1002. doi: 10.1111/j.1445-1433.2004.03220.x

80. Zhang Q-X, Magovern CJ, Mack CA, Budenbender KT, Ko W, Rosengart TK. Vascular Endothelial Growth Factor Is the Major Angiogenic Factor in Omentum: Mechanism of the Omentum-Mediated Angiogenesis. Journal of Surgical Research. 1997 Feb;67(2):147–54. doi: 10.1006/jsre.1996.4983


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Shevlyuk N.N., Khalikova L.V., Khalikov A.A. Morphofunctional Characteristic of the Greater Omentum. Journal of Anatomy and Histopathology. 2020;9(2):90-99. (In Russ.) https://doi.org/10.18499/2225-7357-2020-9-2-90-99

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