scholarly journals Macroscopic assessment of protective effect of cryopreserved placenta extract in ibuprofen-induced gastroenterocolonopathy

2021 ◽  
Vol 55 (3) ◽  
pp. 172-179
Author(s):  
F.V. Hladkykh
Keyword(s):  
Gastrointestinal Tract ◽  
Mucous Membrane ◽  
Large Intestine ◽  
Experimental Studies ◽  
Male Rats ◽  
Intragastric Administration ◽  
Gastroprotective Activity ◽  
Gastrointestinal Lesions ◽  
Small And Large Intestine

Background. Over-the-counter use of nonsteroidal anti-inflammatory drugs leads to their uncontrolled consumption among the population, which in some cases makes it impossible to prevent and timely detect adverse drug effects, and their effectiveness does not always satisfy clinicians. The purpose was to characterize the cytoprotective properties of cryopreserved placenta extract according to the condition of the mucous membrane of the proximal (esophagus and stomach) and distal (small and large intestine) parts of the gastrointestinal tract on the model of ibuprofen-induced esophagogastroenterocolonopathy. Mate­rials and methods. In vivo experimental studies were performed on 28 male rats. Subchronic ibuprofen-induced gastrointestinal lesions were reproduced by intragastric administration of ibuprofen to rats at a dose of 310 mg/kg. The condition of the gastrointestinal tract mucous membrane was assessed macroscopically on a scale. Results. The therapeutic and prophylactic efficacy of esomeprazole statistically significantly (р < 0.05) took place in the proximal parts of the gastrointestinal tract but had little effect on the prevalence of ulcerative lesions in the intestine. At the same time, unlike esomeprazole, which is known to have only gastroprotective activity, cryopreserved placenta extract had a cytoprotective effect both in the stomach and in the distal parts of the gastrointestinal tract — small and large intestine. Thus, the prevalence of ibuprofen-induced both entero- and colonopathy on the background of the study of the extract was almost twice lower than in rats that did not receive correction drugs. Conclusions. It is established that the use of cryopreserved placenta extract in the treatment-and-prophylactic mode has comparable to esomeprazole gastroprotective activity. In addition, it was found that the use of the studied cryoextract was accompanied by a decrease in the multiplicity of ulcerative defects in the small and large intestine of rats, by 4.6 and 3.8 times, respectively, compared to the control animals.

scholarly journals ANTIULCEROGENIC EFFECT OF CRYOPRESERVED PLACENTA EXTRACT AND THE EFFECT OF LOW TEMPERATURES ON THE DIGESTIVE TRACT INJURED BY DICLOFENAC SODIUM IN THE EXPERIMENT

2021 ◽  
Vol 9 (3) ◽  
Author(s):  
Fedir. V. Hladkykh ◽  
Mykola O. Chyzh
Keyword(s):  
Digestive Tract ◽  
Mucous Membrane ◽  
Large Intestine ◽  
Low Temperatures ◽  
Diclofenac Sodium ◽  
Male Rats ◽  
Antiulcer Activity ◽  
Ulcer Index ◽  
Ulcerogenic Effect ◽  
Small And Large Intestine

Today, the ulcerogenic effect of nonsteroidal anti-inflammatory drugs is a key factor that significantly limits their clinical use and is a serious medical and social problem, as these drugs are among the most commonly used drugs – they are used annually by about 5­–7% of the world's population. The aim is to characterize the antiulcerogenic effect of cryopreserved placenta extract and its application against the background of low temperatures in the model of diclofenac sodium-induced ulcerogenesis in rats according to macroscopic studies of the proximal and distal digestive tract. The study was performed on 42 male rats weighing 200–220 g. Acute diclofenac sodium-induced gastrointestinal damage was replicated by a single intragastric administration of diclofenac sodium to rats at a dose of 50 mg/kg. Euthanasia of animals was performed after 24 hours. The condition of the mucous membrane of the digestive tract was assessed on a scale and calculated integrated indicators – ulcer index and antiulcer activity. Cryocell-cryoextract of placenta was administered to rats intramuscularly at a dose of 0.16 ml/kg body weight. Cryoirrigation was performed once by local injection of liquid nitrogen vapor (temperature – 120˚C) for 10 s. It was found that diclofenac sodium at a dose of 50 mg/kg led to erosive-ulcerative damage to the gastric mucosa in 100% of rats, and the ulcer index was 3.9. The most pronounced leveling of the ulcerogenic effect of diclofenac sodium was observed against the combined preventive use of placental cryoextract and low temperature effect – the ulcer index was 12.6 times lower than that of rats with diclofenac sodium-induced ulcerogenesis without correction. Macroscopic evaluation of the distal gastrointestinal tract showed that the introduction of diclofenac sodium led to a statistically significant (p < 0.05) lesion of the mucous membrane of the small and large intestine in 42.9% of rats. According to the magnitude of antiulcer effect (%) in the model of diclofenac sodium-induced ulcerogenesis, the investigated prophylactic approaches for antiulcer activity have the following priority: action of low temperatures + cryoextract of placenta (96.7%) > cryoextract of placenta (92.1%) ~ esomeprazole (88.2%) > action of low temperatures (72.1%). No lesions of both the small and large intestine on the background of the introduction of placental cryoextract in the model of diclofenac sodium-associated ulcerogenesis were detected.

scholarly journals GENERAL ANATOMICAL CHARACTERISTICS OF SMALL INTESTINE IN WHITE RATS

2018 ◽  
Vol 18 (4) ◽  
pp. 88-93 ◽  
Author(s):  
V. H. Hryn
Keyword(s):  
Small Intestine ◽  
Large Intestine ◽  
Acid Corrosion ◽  
White Male ◽  
Experimental Studies ◽  
Physiological Saline ◽  
Male Rats ◽  
Anatomical Features ◽  
White Rats ◽  
Small And Large Intestine

Introduction. The structure of the small intestine in humans and white rats are quite similar. The study of its specific features in white rats is important to supplement and update modern morphological science with data on the course and modelling of certain pathological conditions. Purpose. A detailed study of the anatomical features of the small intestine in white rats is a prerequisite for planning and conducting certain experimental studies. Material and methods. The study was performed on 80 white male rats. The material for the study included removed stomachs with the distal segment of oesophagus, the small and large intestine. Following the removal the organs were fixed with 10% neutral formalin, outer and inner (mucosal) surfaces then were photographed. In other cases, the gastrointestinal tract of animals was filled through the oesophagus with air, physiological saline, and autopolymer plastic (Latacryl-S), and then exposed to acid corrosion, obtaining three-dimensional casts of internal cavities of the stomach, small and large intestine. Results. Having studying the anatomical features of the small intestine of white rats we can distinguish two parts: the initial extra mesenteric part, which can be called the duodenum only by analogy with a similar human section, and its other mesenteric part, in the looped segment of which the border between which the ileal and jejunum division was not found. This segment seems to be designed mainly for the transitive movement of food into the cecum, where their final processing and the formation of faecal masses occur. On the outer surface of the mesenteric small intestine, there are clearly visible groups of lymphoid nodules, known as Peyer's patches.

Description of the gastrointestinal tract and associated organs of the kultarr (Antechinomys laniger)

2013 ◽  
Vol 35 (1) ◽  
pp. 39 ◽  
Author(s):  
Hayley J. Stannard ◽  
Julie M. Old
Keyword(s):  
Gastrointestinal Tract ◽  
Digestive Tract ◽  
Large Intestine ◽  
Cell Types ◽  
Post Mortem ◽  
Microscopic Description ◽  
Future Studies ◽  
New Information ◽  
Small And Large Intestine

This paper provides a macro- and microscopic description of the digestive tract of the kultarr (Antechinomys laniger), a small dasyurid marsupial. The digestive tract was simple, with no external differentiation between the small and large intestine, and lacked a caecum. Mean gross length of the kultarr digestive tract was 165.2 ± 32.1 mm. Microscopically, the tissues had cell types similar to those of other mammals. The new information will aid future post-mortem investigations of captive kultarrs and future studies of nutrition.

5-ALA/PpIX fluorescent diagnostics of stressed-induced small and large intestine neoplasia in laboratorial rats in vivo

2019 ◽  
Author(s):  
Ekaterina G. Borisova ◽  
Alexander Khorovodov ◽  
Ilana Agranovich ◽  
Aysel Mamedova ◽  
Andrey Terskov ◽  
...  
Keyword(s):  
Large Intestine ◽  
Small And Large Intestine

Increased glucose uptake by intestinal mucosa and muscularis in hypermetabolic sepsis

1991 ◽  
Vol 261 (2) ◽  
pp. G287-G294 ◽  
Author(s):  
C. H. Lang ◽  
J. C. Obih ◽  
G. J. Bagby ◽  
J. N. Bagwell ◽  
J. J. Spitzer
Keyword(s):  
Blood Flow ◽  
Gastrointestinal Tract ◽  
Glucose Uptake ◽  
Intestinal Blood Flow ◽  
Similar Extent ◽  
Relative Contribution ◽  
Entire Small Intestine ◽  
Elevated Rate ◽  
Small And Large Intestine

The purpose of the present study was to determine the following: 1) whether the sepsis-induced increase in glucose uptake was a generalized response along the entire length of the gastrointestinal tract; 2) the relative contribution of the mucosa and muscularis to the enhanced uptake; and 3) whether reducing intestinal blood flow would attenuate the elevated rate of glucose uptake. Hypermetabolic sepsis increased in vivo glucose uptake in all sections of the gastrointestinal tract (57-93%) except the stomach. The rates of glucose uptake per gram of tissue by the mucosa and muscularis were not different. However, because the mucosa accounted for the majority of the whole intestine mass, this layer was responsible for 76-78% of the glucose uptake by the entire small intestine. Intestinal blood flow, determined with the use of radiolabeled microspheres, increased by 127% in sepsis. In both groups, approximately 70% of the total intestinal blood flow was distributed to the mucosa. Somatostatin was infused to produce splanchnic vasoconstriction and decreased the sepsis-induced increment in intestinal flow to the mucosa and muscularis (38 and 54%), whereas the enhanced rate of glucose uptake was not altered. Somatostatin also produced a severe insulinopenia. These results indicate that hypermetabolic sepsis increases glucose uptake to a similar extent along the length of the small and large intestine and that the majority of this increase is due to an enhanced uptake by the mucosa.(ABSTRACT TRUNCATED AT 250 WORDS)

scholarly journals Contribution of rat liver and gastrointestinal tract to whole-body protein synthesis in the rat

1980 ◽  
Vol 186 (1) ◽  
pp. 381-383 ◽  
Author(s):  
M A McNurlan ◽  
P J Garlick
Keyword(s):  
Protein Synthesis ◽  
Gastrointestinal Tract ◽  
Rat Liver ◽  
Large Intestine ◽  
Whole Body ◽  
Body Protein ◽  
Small And Large Intestine

The rate of protein synthesis was assessed in liver, stomach, small and large intestine and in the whole body of rats by injection of 100 mumol of [14C]leucine/100 g body wt. In each of the tissues turnover was very rapid, so that taken together they accounted for 43% of the protein synthesized by the whole animal.

scholarly journals A Metabolomic-Based Evaluation of the Role of Commensal Microbiota throughout the Gastrointestinal Tract in Mice

2018 ◽  
Vol 6 (4) ◽  
pp. 101 ◽  
Author(s):  
Yuri Yamamoto ◽  
Yumiko Nakanishi ◽  
Shinnosuke Murakami ◽  
Wanping Aw ◽  
Tomoya Tsukimi ◽  
...  
Keyword(s):  
Small Intestine ◽  
Gastrointestinal Tract ◽  
Large Intestine ◽  
Rrna Gene ◽  
Commensal Microbiota ◽  
Flight Mass Spectrometry ◽  
Specific Pathogen ◽  
Gastrointestinal Microbes ◽  
Small And Large Intestine

Commensal microbiota colonize the surface of our bodies. The inside of the gastrointestinal tract is one such surface that provides a habitat for them. The gastrointestinal tract is a long organ system comprising of various parts, and each part possesses various functions. It has been reported that the composition of intestinal luminal metabolites between the small and large intestine are different; however, comprehensive metabolomic and commensal microbiota profiles specific to each part of the gastrointestinal lumen remain obscure. In this study, by using capillary electrophoresis time-of-flight mass spectrometry (CE-TOFMS)-based metabolome and 16S rRNA gene-based microbiome analyses of specific pathogen-free (SPF) and germ-free (GF) murine gastrointestinal luminal profiles, we observed the different roles of commensal microbiota in each part of the gastrointestinal tract involved in carbohydrate metabolism and nutrient production. We found that the concentrations of most amino acids in the SPF small intestine were higher than those in the GF small intestine. Furthermore, sugar alcohols such as mannitol and sorbitol accumulated only in the GF large intestine, but not in the SPF large intestine. On the other hand, pentoses, such as arabinose and xylose, gradually accumulated from the cecum to the colon only in SPF mice, but were undetected in GF mice. Correlation network analysis between the gastrointestinal microbes and metabolites showed that niacin metabolism might be correlated to Methylobacteriaceae. Collectively, commensal microbiota partially affects the gastrointestinal luminal metabolite composition based on their metabolic dynamics, in cooperation with host digestion and absorption.

Significance of experimental studies for assessing adverse effects of endocrine-disrupting chemicals

2003 ◽  
Vol 75 (11-12) ◽  
pp. 2125-2141 ◽  
Author(s):  
L. E. Gray ◽  
P. M. D. Foster
Keyword(s):  
Adverse Effects ◽  
Statistical Power ◽  
Experimental Studies ◽  
Male Rats ◽  
Male Rat ◽  
High Dose ◽  
Tier 2 ◽  
In Vivo Assays ◽  
Endocrine Disrupting

The U.S. Environmental Protection Agency (USEPA) is developing an endocrine disruptor screening and testing program to detect chemicals that alter hypothalamic-pituitary-gonadal (HPG) function, estrogen, androgen, and thyroid (EAT) hormone synthesis or metabolism and induce androgen (AR) and estrogen (ER) receptor-mediated effects in mammals and other animals. The utility of this approach is based upon the knowledge that mechanisms of endocrine-disrupting chemical (EDC) action are highly conserved at the cellular and molecular levels among vertebrates. Some EDC mechanisms also are shared with invertebrates. High-priority chemicals would be evaluated in a Tier 1 screening (T1S) battery, and chemicals that are positive in T1S would then be tested in Tier 2 (T2). T1S includes in vitro ER and AR receptor binding and/or gene expression, an assessment of steroidogenesis and mammalian (rat) and nonmammalian (fish) in vivo assays. In vivo, the uterotropic assay detects estrogens and antiestrogens, while steroidogenesis, antithyroid activity, antiestrogenicity, and HPG function are assessed in a pubertal female assay. Antiandrogens are detected in the Hershberger assay (weight of androgen-dependent tissues in castrate-immature-male rats). Fish and amphibian assays are also being developed to identify EDCs. Several alternative mammalian in vivo assays have been proposed. Of these, a short-term pubertal male rat assay appears most promising. T1S is designed to be sensitive to EAT activities, but many of the effects detected at the screening level would not be considered adverse, the dosage levels may be high, and the route of administration used may not be the most relevant. However, issues of adversity, dose response, and route(s) of exposure would be resolved in the testing phase. In addition to using an enhanced multigenerational test for Tier 2, an in utero-lactational screening protocol is also being evaluated by USEPA for use in T2 or T1S. For T2, the numbers of endocrine-sensitive end-points and offspring (F1) examined in multigenerational tests need to be expanded for EDCs in a thoughtful manner, based in part upon the results of T1S. In addition, for some chemicals histological examination of 10 adult F1 per sex in only the control and high-dose groups provides inadequate statistical power to detect low-dose lesions induced during development. In these cases, we propose that all the offspring be examined after puberty for gross and histological reproductive abnormalities. Since EDCs, like the phthalates and AR-antagonists, produce characteristic profiles, or syndromes, of adverse effects, data need to be reported in a manner that clearly identifies the proportion of animals displaying one or more of the abnormalities in a syndrome. Consideration should be given to tailoring T2, based on the results of T1S to assure that all of the effects in such chemically induced developmental syndromes are included in the study.

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