Morphofunctional changes in the rat's liver of different ages after L-methionine administration
DOI:
https://doi.org/10.12775/JEHS.2022.12.01.010Keywords
methionine, liverAbstract
Background: Literature data on the effect of methionine on functional activity and, especially, on morphological changes in the liver parenchyma in animals of different ages are sporadic, and research results are often ambiguous.
Aim: The purpose of this work was to study and compare the morphofunctional changes in the liver of rats of different ages on prolonged administration of L-methionine.
Material and Methods: The experiment was performed on 48 male Wistar rats of 3 and 15 months of age. Animals of the experimental group received L-methionine at a dose of 250 mg/kg body weight in addition to the standard diet, daily for 21 days. Histological preparations were prepared from liver tissue by a standard technique. Morphometry was performed on digital images using the computer program «Image J». Succinate dehydrogenase activity and protein concentration were determined in the suspension of hepatocyte mitochondria.
Results: It was revealed that 21-day administration of L-methionine to rats led to hypertrophy of the hepatocyte nucleus, an increase in the nuclear-cytoplasmic ratio, the number of binuclear hepatocytes, and the nucleolus in the cell nucleus. The relative area of the sinusoids network increased by 50% in 3-month-old animals. This indicated a better blood filling of the liver parenchyma. The increase in succinate dehydrogenase activity and protein concentration was revealed in the suspension of hepatocyte mitochondria of the experimental rats. This indicated an increase in the mitochondria energy potential and protein-synthetic activity.
Conclusions: The administration of prophylactic doses of methionine to healthy rats leads to the appearance of pronounced morphological and functional signs of increased activity of hepatocytes. The severity of this effect has a distinct age-dependent character. In young rats, it is more pronounced than in mature rats. The results of the study are important for practical medicine when using methionine for therapeutic and prophylactic purposes.
References
Li Z, Wang F, Liang B, et al. Methionine metabolism in chronic liver diseases: an update on molecular mechanism and therapeutic implication. Sig Transduct Target Ther. 2020; 5:280. doi: 10.1038/s41392-020-00349-7.
Geltink R, Pearce E. The importance of methionine metabolisme. Life. 2019; 8:e47221. doi: 10.7554/eLife.47221.
Best CH, Ridout JH. The lipotropic action of methionine. J Physiol. 1940; 97(4):489-94.
Chandler TL, White HM. Choline and methionine differentially alter methyl carbon metabolism in bovine neonatal hepatocytes. PLoS One. 2017; 12(2):e0171080.
Mato JM, Martínez-Chantar ML, Lu SC. S-adenosylmethionine metabolism and liver disease. Ann Hepatol. 2013; 12(2):183-89.
Lieber CS. S-adenosyl-L-methionine: its role in the treatment of liver disorders. Am. J. Clin. Nutr. 2002; 76(5):1183S-1187S.
Caballero F, Fernández A, Matías N, et al. Specific contribution of methionine and choline in nutritional nonalcoholic steatohepatitis: impact on mitochondrial S-adenosyl-L-methionine and glutathione. J Biol Chem. 2010; 285(24):18528-36. doi: 10.1074/jbc.M109.099333.
Latimer MN, Freij KW, Cleveland BM, et al. Physiological and molecular mechanisms of methionine restriction. Front Endocrinol (Lausanne). 2018; 9:217. doi:10.3389/fendo.2018.00217.
Stojanović M, Todorović D, Šćepanović L, et al. Subchronic methionine load induces oxidative stress and provokes biochemical and histological changes in the rat liver tissue. Mol Cell Biochem. 2018; 448(1-2):43-50. doi: 10.1007/s11010-018-3311-2.
Gabuniya L, Bakuridze K, Gogolauri M, et al. Vliyaniye karvediola, metionina i ikh kombinatsii na nekotoryye funktsional'nyye parametry pecheni i morfologicheskiye izmeneniya v usloviyakh toksicheskogo gepatita. [Influence of carvediol, methionine and their combination on some functional parameters of the liver and morphological changes in the conditions of toxic hepatitis]. Allergologiya i immunologiya. 2010; 11(2):106-8. (in Russsan).
Danilov RK. Rukovodstvo po gistologii. Tom ÍÍ. [Guide to histology. Volume II.]. St. Petersburg: SpecLith; 2011. (in Russian).
Yanko R, Berezovskii V, Chaka E, et al. Morphofunctional characteristic of hepatocytes after exposure to intermittent normobaric hypoxia in normotensive and hypertensive rats. Regulatory Mechanisms in Biosystems. 2017; 8(2):265-70. doi: 10.15421/021741.
Rudzki Z, Szczudrawa J, Stachura J. Morphometry of normal, regenerating and cancerous hepatocytes. Folia Histochem Cytobiol. 1999; 27(3):141-8.
Rauterberg J, Voss B, Pott G, et al. Connective tissue components of the normal and fibrotic liver. Klin Wochenschr. 1981; 59:767-79. doi:10.1007/BF01724682.
Rutter J, Winge DR, Schiffman JD. Succinate dehydrogenase – Assembly, regulation and role in human disease. Mitochondrion. 2010; 10(4):393-401. doi: 10.1016/j.mito.2010.03.001.
Allen JF. Why chloroplasts and mitochondria retain their own genomes and genetic systems: Colocation for redox regulation of gene expression. PNAS. 2015; 112(33):10231-238. doi: 10.1073/pnas.1500012112.
Rosioru C, Talu S, Talu M, et al. Morphometric assessments for the healthy rat hepatocytes. Annals of the Romanian Society for Cell Biology. 2012; XVII(1):74-9.
Duncan AW, Taylor MH, Hickey RD, et al. The ploidy conveyor of mature hepatocytes as a source of genetic variation. Nature. 2010;467(7316):707-10. doi: 10.1038/nature09414.
Sarkisov DS, Vtyurin BV. Elektronnaya mikroskopiya destruktivnykh i regeneratornykh vnutrikletochnykh protsessov. [Electron microscopy of destructive and regenerative intracellular processes]. Moscov: Medicine; 1967. (In Russian).
Romanova LP, Malyshev II. Rol' dvuyadernykh gepatotsitov v regeneratsii pecheni posle mekhanicheskoy travmy v rannem ontogeneze u krys [The role of binuclear hepatocytes in liver regeneration after mechanical trauma in early ontogenesis in rats]. Vestnik Chuvashskogo universiteta. 2011; 3:398-402. (in Russian).
Boisvert F, van Koningsbruggen S, Navascués J, et al. The multifunctional nucleolus. Molecular Cell Biology. 2007; 8(7):574-85. doi:10.1038/nrm2184.
Stawiarska-Pięta B, Bielec B, Birkner K, et al. The influence of vitamin E and methionine on the activity of enzymes and the morphological picture of liver of rats intoxicated with sodium fluoride. Food Chem Toxicol. 2012; 50(3-4):972-8. doi: 10.1016/j.fct.2012.01.014.
Pivtorak KV. Submikroskopichnyy stan pechinky pry korektsiyi steatozu hepatoprotektorom aminokyslotnoho pokhodzhennya [Submicroscopic condition of the liver in the correction of steatosis with hepatoprotector of amino acid origin]. Visnyk problem biolohiyi ta medytsyny. 2015; 3(2):310-13. (in Ukraine).
Itagaki H, Shimizu K, Morikawa S, et al. Morphological and functional characterization of non-alcoholic fatty liver disease induced by a methionine-choline-deficient diet in C57BL/6 mice. Int J Clin Exp Pathol. 2013; 6(12):2683-96.
Hirche F, Schröder A, Knoth B, et al. Effect of dietary methionine on plasma and liver cholesterol concentrations in rats and expression of hepatic genes involved in cholesterol metabolism. Br J Nutr. 2006; 95(5):879-88.
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