EPITHELIAL ENDOCRINE CELLS OF THE COLON MUCOSA OF MAMMALS

Annotasiya

The structure of the intestines of mammals and humans is very similar. The large intestine consists of the colon, cecum, sigmoid colon and rectum. The structure of the intestinal wall (regardless of the section) is usually divided into mucosal, submucosal, muscular and serous layers. The intestinal mucosa consists of single-layer columnar epithelium of the intestinal type. In mammals, the length of the colon varies and is mainly species-specific, reaching up to 1.4 meters in humans. In rats it is 35-47 cm.

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Choriev , E. ., & Bahronov, J. . (2025). EPITHELIAL ENDOCRINE CELLS OF THE COLON MUCOSA OF MAMMALS. Наука и технология в современном мире, 4(1), 136–138. Retrieved from https://www.inlibrary.uz/index.php/zdift/article/view/63016
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Annotasiya

The structure of the intestines of mammals and humans is very similar. The large intestine consists of the colon, cecum, sigmoid colon and rectum. The structure of the intestinal wall (regardless of the section) is usually divided into mucosal, submucosal, muscular and serous layers. The intestinal mucosa consists of single-layer columnar epithelium of the intestinal type. In mammals, the length of the colon varies and is mainly species-specific, reaching up to 1.4 meters in humans. In rats it is 35-47 cm.


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EPITHELIAL ENDOCRINE CELLS OF THE COLON MUCOSA OF MAMMALS

Choriev Elyor Bahodirovich

Bahronov Jurat Jurakulovich

Bukhara State Medical Institute, Bukhara.

e-mail: elyor47771189@mail.ru

https://doi.org/10.5281/zenodo.14698249

The structure of the intestines of mammals and humans is very similar. The large intestine

consists of the colon, cecum, sigmoid colon and rectum. The structure of the intestinal wall
(regardless of the section) is usually divided into mucosal, submucosal, muscular and serous
layers. The intestinal mucosa consists of single-layer columnar epithelium of the intestinal type.
In mammals, the length of the colon varies and is mainly species-specific, reaching up to 1.4
meters in humans. In rats it is 35-47 cm.

The mucous membrane of the colon has its own relief, forming crescent-shaped folds and

crypts. The morphometric characteristics of these formations in animals depend on the type of
animal, that is, the type of structure and type of nutrition [1,9].

Epithelial cells are divided into absorptive, absorptive, goblet, endocrine, Paneth cells and

stem cells. Absorptive epithelial cells consist of two types of cells: bordered and un bordered.
The main function of these cells is to ensure absorption processes. The degree of differentiation
of goblet cells varies depending on their location. Less differentiated cells are located at the
bottom of the crypts. The crypts of endocrine epithelial cells differ in the composition and shape
of the secretion. Paneth cells are located in the crypts, and some literature states that Paneth
cells are absent from the colonic mucosa [7,3].

Normally, the mucous membrane of the large intestine (colon) of mammals is

characterized by the formation of folds, allowing for expansion of the inner surface of the
intestine. Also in the colon there are many unbranched crypts, in the lower parts of which there
is a small group of stem cells. The depth of the colon crypts varies depending on the species and
linear age of the animal (in adult rats 187 ± 73 µm, in mice 187 ± 208 µm). The intercrypt spaces
are filled with porous fibrous unformed connective tissue. The crypts contain goblet cells that
produce large amounts of mucus, protect the surface of the mucosal epithelium and allow the
easy sliding movement of feces. In the lamina privata of the mucous membrane we see the
accumulation of a large amount of lymphoid tissue [15,8].

The structure of the mammalian rectal epithelium changes from columnar epithelium

caudally to stratified cuboidal epithelium, and then abruptly to stratified squamous non-
keratinizing epithelium, which gradually gives way to cutaneous-type epithelium
(keratinizing). Crypts in the rectal mucosa are deeper than in the colon, but are located less
frequently. The crypts disappear in the lower rectum [2,13].

The epithelium contains a large number of intraepithelial lymphocytes that perform a

protective function against a sharply increased number of bacteria (according to some data, up
to 75% of feces consists of dead and living bacteria).

In the lamina privata of the mucous membrane there are a large number of lymphoid

nodes, sometimes lymphoid nodes are replaced by large ones, but there are no Peyer’s patches,
as in the small intestine [4,12].


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The muscular plate of the mucous membrane consists of an inner circular and outer

longitudinal layer of smooth myocytes. The submucosal layer consists of loose fibrous
connective tissue.

The muscle layer consists of two layers: the inner circular and the outer longitudinal-

longitudinal, which do not completely cover the large intestine, but form three longitudinal
stripes. They are shorter than the large intestine, so in appearance they resemble an
“accordion” [3].

The serous layer, on the contrary, consists of loose fibrous unformed connective tissue

and mesothelium containing adipose tissue, as well as sebaceous tumor-like appendages.

The endocrine gastroenteropancreatic system (GEP-system) is a collection of endocrine

cells that are diffusely located in the epithelium of the mucous membrane of the digestive
system of vertebrates.

75% of the endocrine system of the GEP consists of endocrinocytes of the DNIE (diffuse

neuroimmunoendocrine) system. Cells of the DNIE system are diffusely located in the mucous
membranes of the entire div and are part of various organs and associated glands. Endocrine
cells can be of different types depending on their origin and location, but they perform the same
functions. This is the absorption of amines, their decarboxylation or the synthesis of biogenic
amines necessary for the formation and activity of peptides (hormones) that regulate them.
DNIE cells are identified by the Grimelius method (argyrophilic cells, the entire population of
endocrinocytes, with the exception of D-cells) and the Masson-Gamperl method (argentaffin
cells), immunohistochemical methods, as well as ultrastructural analysis [6, 10].

The elements of the endocrine system of the GEP include cells of the pancreatic islets of

the pancreas, endocrinocytes of the epithelium of the digestive tract (from the esophagus to the
rectum). In the pancreas, endocrinocytes are compact (in the form of islets of Langerhans)
between exocrine cells and isolated, while in other organs (including the intestine) they are
located diffusely in the epithelium of the mucous membrane. In the cytogenesis of endocrine
cells, one can distinguish: stem cells, agranular cells, endocrinocytes, which subsequently
differentiated into various endocrine cells of the GEP system due to an increase in the number
of membrane structures in the cytoplasm and the accumulation of endocrine granules, as well
as cells that became endocrinocytes as a result of the transformation of exocrine cells [ 11.14].

Among the endocrine cells of the intestine, open and closed endocrinocytes can be

distinguished. The apical part of open-type endocrine cells reaches the surface of the mucous
membrane, contains several microvilli and performs receptor functions. They sense chemical
influences and pH changes in the stomach. Closed endocrinocytes do not communicate with the
crypt cavity; they stimulate secretion as a result of various influences (pressure, temperature
changes, etc.). In the basal part of the cytoplasm of endocrine cells there are secretory granules
containing polypeptides and monoamines. The shape, size and composition of secretory
granules serve as the basis for the classification of these cells. Secretions from endocrinocytes
can enter the intercellular space and then into the blood and directly affect target cells
(paracrine and endocrine secretory pathways). In the cells of the GEP system, in addition to
endocrinocytes, there are exocrine and endocrine “mixed” cells that simultaneously contain
two types of secretory granules in the cytoplasm (exoendocrine cells), and endocrinocytes that
simultaneously contain granules with different endocrine properties. in their cytoplasm.


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International Journal of Pharmaceutical Research (09752366)

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Bibliografik manbalar

Anisimov V.N. Melatonin role in the body, clinical use / V.N. Anisimov. – St. Petersburg: “System”, 2007. – 40 p.

Barinov E.F. The role of serotonin in the physiology and pathology of gastrointestinal tract intestinal tract / E.F. Barinov, O.N. Sulaeva // Russian Journal gastroenterology, hepatology, coloproctology. – 2012. – T. 2. – P. 4-13.

Bakronov, Zh. Zh. (2022). Morphological and Functional Changes in the Kidney with Toxic Damage to the Liver. Central Asian Journal of Medical and Natural Science, 3(5), 332-335.

Bakronov, Zh. Zh., & Teshaev, Sh. Zh. (2020). Morphometric characteristics of parts of the kidney nephron in rats under normal conditions and when exposed to the antiseptic Dorogoff stimulant fraction 2 against the background of chronic radiation sickness. Problems of biology and medicine, (4), 138-140.

Zvenigorodskaya L.A. Changes in the colon in patients with metabolic syndrome / L.A. Zvenigorodskaya // Bulletin of Family Medicine: Gastroenterology. – 2014. – No. 1. – P. 48-55.

Kim A.D. Features of topographic anatomy and parietal microflora of the distal colon in Wistar rats / A.D. Kim, O.A. Goldberg, S.A. Lepekhova [and others] // Bulletin of the All-Russian Scientific Center of the Siberian Branch of the Russian Academy of Medical Sciences. – 2016. – T. 1, No. 2. – pp. 48-54.

Lukashenko T.M. The influence of soybean oil on the morphological characteristics of the colon of rats under conditions of experimental colitis / T.M. Lukashenko, A.I. Sherstyak, E.V. Martsinkevich // Reports of the National Academy of Sciences of Belarus. – 2013. – T. 57, No. 1. – pp. 102-106.

Nimiritsky P.P. Stem cell niche. / P.P. Nimiritsky, G.D. Sagaradze, A.Yu. Efimenko, P.I. Makarevich, V.A. Tkachuk. // Cytology. – 2018. – T. 60, No. 8 – P. 575-586.

Poluektov M.G. Possibilities for correcting insomnia in elderly patients / M.G. Poluektov, E.A. Lyashenko // Effective pharmacotherapy. Neurology and psychiatry. – 2014. – T. 22, special issue No. 2. – pp. 44-47.

Cheremushkin S.V. Evidence-based studies in the treatment of irritable bowel syndrome / S.V. Cheremushkin // Academic journal of Western Siberia. – 2014. – T. 10, No. 3. – pp. 33-35.

BAKHRONOV, J. A. J., TESHAEV, S. J., & SHODIEVA, M. S. (2021). Morphometric characteristics of parts of rat kidney nephron in normal and under the influence of an antiseptician-facility 2 road stimulator on the background of chronic radiating disease. International Journal of Pharmaceutical Research (09752366), 13(1).

Bertrand R.L. Serotonin availability in rat colon is reduced during a Western diet model of obesity / R.L. Bertrand, S. Senadheera, A. Tanoto [et al.] // American Physiological Gastrointestinal and Liver Physiology. – 2012. – Vol. 303. – P. 424-434.

Burman D. Sleep Disorders: Circadian Rhythm Sleep-Wake Disorders / D. Burman – 2017. – F.P. Essent. – Vol. 460. – P. 33-36.

Dierickx P. Circadian clocks: from stem cells to tissue homeostasis and regeneration / P. Dierickx, L.W. Van Laake, N. Geijsen // EMBO Rep. – 2018. – Vol. 19, N 1. – P. 18-28.

Lemoine P. Prolonged-release formulation of melatonin (Circadin) for the treatment of insomnia / P. Lemoine, N. Zisapel // Expert. Opin. Pharmacother. – 2012. – Vol. 13, N 6. – P. 895-905.