Submission of the manuscript is online via e-mail
ecgarticle@gmail.com or
cholerez@mail.ru

Tel: +7 903 250 5288

Editorial Correspondence e-mail
gastrossr@gmail.com


Publishing, Subscriptions, Sales and Advertising, Correspondence e-mail
journal@cniig.ru

Tel: +7 917 561 9505

SCImago Journal & Country Rank

    1. GBU the MСRC named after A. S. Loginov DZ Moscow, 111123 Moscow, Russia
    2. Peoples ' friendship University of Russia, Moscow, Russia
    3. National research Mordovian state University. N. P. Ogaryov, Saransk, Russia

    Keywords: mucous membrane of the gastrointestinal tract, autoimmune component, immune system of the gastrointestinal tract, M-cells

    Abstract:The mucous membrane of the gastrointestinal tract is an extensive information and communication system that quickly reacts to both external and internal factors of the body, ensuring the maintenance of homeostasis of tissue and blood. The aim of the study was to determine the factors that ensure the appearance of an autoimmune component in damage to the pancreas in rats. Material: manipulations were performed on white Wistar rats weighing 190,0–230,0.Immunization of animals was carried out according to the standard scheme. There were 4 intraperitoneal injections of 2 ml of pancreatic tissue homogenate. Total antibodies (at) to parietal cells (PC) (Parietal Cell antibodies, IgG, IgA, IgM) were determined in plasma by enzyme immunoassay. The animals were divided into one control group and fi ve experimental groups (6 groups of 5 rats in total). Experimental groups: 1st-immunization of intact animals (IM) according to the above scheme. 2nd-acute pancreatitis (AP); 3rd group AP+ IM; 4th-chronic pancreatitis (CP); 5th group-CP+IM. With AP and CP, there is an autoimmune component that interferes with the restoration of damaged pancreatic tissue. Experimental studies have shown that the presence of acute infl ammation, accompanied by full blood vessels, hyperemia, edema, hypoxia, necrosis, death of a large number of cells, the release of cellular elements that are endogenous antigens. Infl ammation of the pancreas stimulates the immune system of the gastrointestinal tract. In addition, factors contributing to the development of an autoimmune reaction are: alcohol, infection: bacterial, viral and/or parasitic.

      1. Yaglov V. V. Yaglova N. V. Itogi i perspektivy izucheniya diff uznoy endokrinnoy epitelialnoy sistemy. Klinicheskaya i eksperimentalnaya morfologiya. 2012. № 3. p.3
      2. Aruin L. I. Zverkov I. V. Vinogradov V. A. Endokrinnyye kletki zheludochno-kishechnogo trakta. Klinicheskaya meditsina. 1987, no. 6, p. 2231.
      3. Kvetnoy I. M. APUD-SISTEMA (strukturno-funktsionalnaya organizatsiya. biologicheskoye znacheniye v norme i patologii). Uspekhi fi ziologicheskikh nauk. 1987, vol. 18. no. 1, p. 84–102.
      4. Aleshin B. V. Problema neyroendokrinnykh kletok i gipotezy “Diff uznoy endokrinnoy sistemy.” Uspekhi sovremennoy biologii. 1984, vol. 98, no. 1(4), p.116–133.
      5. Korotko G. F. Fiziologiya sistemy pishchevareniya. OOO BK “Gruppa B” Krasnodar. 2009, 608 p.
      6. Sapin M. R. Immunnyye struktury pishchevaritelnoy sistemy. Meditsina. 1987, 224 p.
      7. Kononov A. V. Mestnyy immunnyy otvet na infektsiyu Helicobacter pylori. Rossiyskiy zhurnal gastroenterologii. gepatologii. koloproktologii. 1999, no.2, pp.15–22.
      8. Jang MH, Kweon MN, Iwatani K, Yamamoto M, Terahara K, Sasakawa C, Suzuki T, Nochi T, Yokota Y, Rennert PD, et al. Intestinal villous M cells: an antigen entry site in the mucosal epithelium. Proc Nat AcadSci U S A 2004; 101:6110–5; PMID:15071180; http:// dx.doi.org/10.1073/pnas.0400969101 [PMC free article] [PubMed] [Cross Ref]
      9. Kyd JM, Cripps AW. Functional diff erences between M cells and enterocytes in sampling luminal antigens. Vaccine 2008; 26:6221–4; PMID:18852006; http://dx.doi. org/10.1016/j.vaccine.2008.09.061 [PubMed] [Cross Ref]
      10. Miller H, Zhang J, Kuolee R, Patel GB, Chen W. Intestinal M cells: the fallible sentinels? World J Gastroenterol: WJG 2007; 13:1477–86; PMID:17461437; http://dx.doi .org/10.3748/wjg.v13.i10.1477 [PMC free article] [PubMed] [Cross Ref]Жуков Н.А., Гусаров А. И. Иммунологические аспекты кишечного дисбактериоза // Терапевтический архив. 1980. – Т. 52, № 2. – С. 23–27.
      11. Proshchina A. E., Savelyev S. V. Immunogistokhimicheskoye issledovaniye raspredeleniya A- i B- kletok v raznykh tipakh ostrovkov Langergansa podzheludochnoy zhelezy cheloveka. Byulleten eksperimentalnoy biologii i meditsiny. 2013, Vol. 155, no.6, p.763. http://www.iramn. ru/journal/bebm/2013/bbm1306.htm
      12. Trubitsyna I. E. Vorobyeva N. N. Chikunova B. Z. Kryukova N. B. Autoimmunnyy komponent pri alkogolnom povrezhdenii pecheni u krys. Eksperimentalnaya i klinicheskaya gastroenterologiya. 2012, no. 12, p.52–54.
      13. Trubitsina I. E. Abdulatipova Z. M. Vasnev O. S. et al. Cerotonin v razvitii i podderzhanii vospalitelnoy reaktsii v slizistoy obolochke zheludka u krys. Fundamentalnyye issledovaniya. 2014, no.10–2, pp. 380–385.
      14. Trubitsyna I. E., Smirnova A. V., Chikunova B. Z., Sokolov D. V. Patogeneticheskoye obosnovaniye korrektsii morfologicheskikh izmeneniy i disbalansa tsitokinov v eksperimentalnoy modeli yazvy zheludka. Lecheniye i profi laktika. 2015, no. 3 (15), pp. 63–68.
      15. Trubitsyna I. E., Smirnova A. V., Chikunova B. Z., Sokolov D. V. Patogeneticheskoye obosnovaniye korrektsii morfologicheskikh izmeneniy i disbalansa tsitokinov v eksperimentalnoy modeli yazvy zheludka. Lecheniye i profi laktika. 2015, no. 3 (15), pp. 63–68.
      16. Trubitsyna I., Onischenko N., Lyundup A., Knyazev O., Parfenov A., Vinocurova L., Orlova Yu., Abdulatipova Z., Ruchkina I., Smirnova A. Иммуномодулирующий эффект аллогенных мезенхимальных стволовых клеток костного мозга крыс// В книге: Abstracts for Cell Technologies at Th e Edge: Research & Practice (CTERP) 2016. С. 121.
     


    Full text is published :
    Trubitsyna I. E., Ruchkin I. N., Mikhailovа S. F., Efremov L. I. et al. MALT-the mucous membrane system of the gastrointestinal tract. Experimental and Clinical Gastroenterology. 2018;159(11): 83–87. (In Russ.) DOI: 10.31146/1682-8658-ecg-159-11-83-87
    Read & Download full text

    1. Pirogov Russian National Research Medical University (RNRMU), Moscow, Russia
    2. Peoples Friendship University of Russia (RUDN), Moscow 117198, Russia

    Keywords: stomach, colon, motor activity, serotonin

    Abstract:Trial objective: study the mechanism of multidirectional eff ect of Serotonin adipinate on gastric and colon motor activity. Materials and methods: experiments were carried out on Wistar rats (N83) in surgical anesthesia. An electromyogram and hydrostatic pressure in the cavities of organs was registered using an amplifi er BioAmp ML132 (Adinstruments, Australia), an analog-to-digital converter Maclab 8e (Adinstruments, Australia), a computer Масintosh Performa 6400/180 and a software program Chart 4.2.3. Trial fi ndings: it was established that intra-arterial injection of Serotonin adipinate at a dose of 0.05 mg/kg and 0.1 mg/ kg causes stimulatory and inhibitory gastric reactions; at a dose of 0.15 mg/kg — only stimulatory ones. Colon appeared to have only stimulatory reactions. It was also found that intravenous injection of Serotonin adipinate does not intensify stomach and colon contraction. Conclusion. Organs’ stimulatory reactions occur due to activation of muscle 5HT-receptors, inhibitory ones — due to activation of presynaptic 5HT-receptors, locating on organ’s adrenergic terminals, and ejection of inhibitory transmitter noradrenaline by them. When using Serotonin adipinate in experiment and in clinical practice, it is necessary to take into account that the organs’ eff ect from serotonin administration into body may be dual: inhibitory at low doses and stimulatory at higher ones.

      1. Davis R., Pattison J., Th ompson J. et al. 5-hydroxytryptamine (5-HT) reduces total peripheral resistance during chronic infusion: direct arterial mesenteric relaxation is not involved. BMC Pharmacol. 2012; V 12: 4.
      2. Arreola-Ramírez J., Vargas D., Manjarrez-Gutiérrez G. et al. Modifi cations of plasma 5-HT concentrations during the allergic bronchoconstriction in guinea pigs. Exp. Lung. Res. 2013; 39 (7): 269–274.
      3. Veasey S. Serotonin agonists and antagonists in obstructive sleep apnea: therapeutic potential. Amer. J. Respir. Med. 2003; 2(1): 21–29.
      4. Tamura T., Sano I., Satoh M. et al. Pharmacological characterization of 5-hydroxytryptamine-induced motor activity (in vitro) in the guinea pig gastric antrum and corpus. Europ. J. Pharmacol. 1996; 308 (3): 315–324.
      5. Овсянников В. И., Березина Т. П. Механизмы влияния серотонина на моторную активность двенадцатиперстной, тощей и подвздошной кишки у бодрствующих кроликов. Рос. физиол. журн. им. И. М. Сеченова 2002; № 8: 1017–1027.
      6. Ovsiannikov V. I., Berezina T. P. Mechanism of the serotonin eff ect on motility of the duodenum, ileum, and jejunum in awake rabbits. Russian journal of physiology. 2002, no.8, pp.1017-1027
      7. van Lelyveld N., Ter Linde J., Schipper M. et al. Serotonergic signalling in the stomach and duodenum of patients with gastroparesis. Neurogastroenterol. Motil. 2008; 20 (5): 448–455.
      8. Sia T., Whiting M., Kyloh M. 5-HT3 and 5-HT4 antagonists inhibit peristaltic contractions in guinea-pig distal colon by mechanisms independent of endogenous 5-HT. Front. Neurosci. 2013; 7: 136.
      9. Song J., Yin J., Chen J. Acute and chronic eff ects of desvenlafaxine on gastrointestinal transit and motility in dogs. Neurogastroenterol. Motil. 2013; 25 (10): 824.
      10. Lee J., Sung K., Lee O. et al. Th e eff ects of 5-HT4 receptor agonist, mosapride citrate, on visceral hypersensitivity in a rat model. Dig. Dis. Sci. 2012; 57 (6): 1517–1524.
      11. Sinenchenko G. I., Verbitskiy V. G., Kolunov A. V. Endolymphatic infusion of serotonin adipinate in the treatment of postoperative intestinal paresis. MIA Medical Bulletin. 2006; no 2, pp. 21–23.
      12. Kale-Pradhan Pramodini B., Wilhelm Sheila M. Tegaserod for constipation-predominant irritable bowel syndrome. Pharmacotherapy. 2007; 27 (2): 267–277.
      13. MacLean M.R., Dempsie Y. Serotonin and pulmonary hypertension – from bench to bedside. Curr. Opin. Pharmacol. 2009; 9 (3): 281–286.
      14. McKenzie C., Alapati V. R., MacDonald A. et al. Mechanisms involved in the regulation of bovine pulmonary vascular tone by the 5HT1B-receptor. Brit. J. Pharmacol 2010; 159 (1): 188–200.
      15. Purohit A., Herrick-Davis K., Teitler M. Creation, expression, and characterization of a constitutively active mutant of the human serotonin 5-HT6-receptor. Synapse. 2003; 47(3): 218–224.
      16. Th umshirn M., Fraehauf H., Stutz B. et al. Clinical trial: Eff ects of tegaserod on gastric motor and sensory function in patients with functional dyspepsia. Alim. Pharmacol. Th er. 2007; 26 (10): 1399–1407.
     


    Full text is published :
    Smirnov V. M., Sveshnikov D. S., Kuchuk A. V., Trubetskaya L. V., Mongush M. I., Ignatova E. D. The mechanism of multidirectional eff ects of serotonin on the motility of the stomach and colon. Experimental and Clinical Gastroenterology. 2018;159(11): 88–92. (In Russ.) DOI: 10.31146/1682-8658-ecg159-11-88-92
    Read & Download full text