Evaluation of exogenous effects of carbohydrate and ethanol solutions on rat liver
DOI:
https://doi.org/10.31548/bio2019.05.003Keywords:
liver, glucose, ethanol, blood, rats, pathological processAbstract
The results of studies of exogenous action of glucose and ethanol solutions on the rat organism with description and demonstration of pathological changes of the liver are presented in the article.
Prolonged action of ethanol and its metabolism products on the liver, especially acetaldehyde, and under conditions of enhancement by other factors (for example, carbohydrate solutions), leads to impaired function and causes significant morphological changes. Morphofunctional disorders of the liver, in turn, can provoke some serious animal complications, one of which is type 2 diabetes. This is due to the crucial role of the liver in the regulation of carbohydrate metabolism.
Type 2 diabetes became a widespread disease in pets in recent years, which is primarily related to their diet. The effects of this disease are reduced productivity, stunted growth and high early mortality in animals.
A study of one of the most important indicators of carbohydrate metabolism - serum glucose content, showed that animals that regularly consumed a carbohydrate solution (by drinking way) for 23 days had a 54% increase in blood glucose, while in rats with additional alcohol load in the diet (ethanol solution in combination with glucose solution) - by 77% compared to control.
Carrying out histological studies in experimental animals revealed the development of pathological changes, which depending on the conditions of the experiment had different severity. In particular, when consuming carbohydrate solution by drinking way, the animals developed: granular hepatocyte dystrophy and histiocytic infiltration of the interparticle connective tissue. In animals treated with a carbohydrate solution in combination with ethanol, granular and hyaline-drip hepatocytes, histiocytic infiltration of the interparticle connective tissue, and cholestasis in the bile ducts were detected.
References
Pro zakhyst tvaryn vid zhorstokoho povodzhennia (2006). [On the Protection of Animals from Cruelty]. Zakon Ukrainy N 27, st. 230. https://zakon.rada.gov.ua/laws/show/3447-15
Bоden G. (1997). Rоle оffаtty аcids inthe pаthоgenesis оf insulinresistаnce аnd NiDDM. Bоden. Diabetes, 46 (3): 3-10.
European convention for the protection of vertebrate animals used for experimental and other scientific purposes. Council of Europe, Strasbourg, 1986, 53 p.
Goto R., Kamimura K., Shinagawa-Kobayashi Y., Sakai N., Nagoya T., Niwa Y., Ko M., Ogawa K., Inoue R., Yokoo T., Sakamaki A., Kamimura H., Abe S., Nishina H., Terai S. (2019) Inhibition of sodium glucose cotransporter 2 (SGLT2) delays liver fibrosis in a medaka model of nonalcoholic steatohepatitis (NASH). FEBS Open Bio. 019 Feb 15;9 (4): 643-652.
https://doi.org/10.1002/2211-5463.12598
Junzhao Y., Xuan H., Tingfeng W., Yanqin W., Congxiang S., Fuxi L., Yansong L., Shiting F., Wei W., Bihui Z (2019). Insulin resistance exhibits varied metabolic abnormalities in nonalcoholic fatty liver disease, chronic hepatitis B and the combination of the two: a cross-sectional study. Diabetology Metabolic Syndrome. Published online 2019 Jun 15. PMCID: PMC 6570947 PMID: 31223344
https://doi.org/10.1186/s13098-019-0440-z
Liangyou R. (2014). Comprehensive Physiology Energy Metabolism in the Liver. Published online: doi:10.1002/cphy.c130024
https://doi.org/10.1002/cphy.c130024
Mona H., Naglaa M., Hala M., Hanan G., Rashed L. (2019). Diabetes Mellitus, Nonalcoholic Fatty Liver Disease, and Conjugated Linoleic Acid (Omega 6): What Is the Link? Journal of Diabetes Research. Article ID 5267025, 7. https://doi.org/10.1155/2019/5267025
Moore M., Smith M., Farmer B., Coate K., Kraft G. (2018). Morning Hyperinsulinemia Primes the Liver for Glucose Uptake and Glycogen Storage Later in the Day. Diabetes 2018;67:1237 - 1245.
https://doi.org/10.2337/db17-0979
Nakashima M., Kinoshita. M., Nakashima H., Kotani A., Ishikiriyama T., Kato S., Hiroi S., Seki S. (2019). Pioglitazone improves phagocytic activity of liver recruited macrophages in elderly mice possibly by promoting glucose catabolism. Innate Immunity.journals.sagepub.com/home/ini.
https://doi.org/10.1177/1753425919849620
Rоbertsоn R., Harmon J., Tran P., Tanaka Y., Takahashi H.(2003) Glucose Toxicity in β-Cells: Type 2 Diabetes, Good Radicals Gone Bad, and the Glutathione Connection. Diabetes 2003 Mar; 52(3): 581-587.
Downloads
Additional Files
Published
Issue
Section
License
Relationship between right holders and users shall be governed by the terms of the license Creative Commons Attribution – non-commercial – Distribution On Same Conditions 4.0 international (CC BY-NC-SA 4.0):https://creativecommons.org/licenses/by-nc-sa/4.0/deed.uk
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).