INFLUENCE OF KETOSIS AND GLYCEMIA LEVELS ON CRAVING FOR ETHANOL IN ALCOHOLIZED RATS

T. Panova, O. Myronenko
{"title":"INFLUENCE OF KETOSIS AND GLYCEMIA LEVELS ON CRAVING FOR ETHANOL IN ALCOHOLIZED RATS","authors":"T. Panova, O. Myronenko","doi":"10.32345/2664-4738.4.2022.03","DOIUrl":null,"url":null,"abstract":"Relevance. In case of developed alcoholic disease, under conditions of alcoholic hypoglycemia, ketone bodies act as an energy substrate for the brain. However, the role of ketone hunger for maintaining the craving for alcohol has not been established. The assumption of such a connection has a right to exist, since it is alcohol that stimulates the formation of ketone bodies. Therefore, with developed alcoholism, the desire to consume alcohol (and, in fact, \"saturate\" the brain with ketone bodies) can be considered as a consequence of hypoketonemia. Accordingly, the hunger of the alcoholic is the result of hypoketonemia, but not hypoglycemia. Therefore, it is relevant to conduct a study in which the given variables (controlled by us) were the level of glycemia and the level of ketonemia, and the amount of alcohol consumed voluntarily (under conditions of free choice) was a derivative and dependent value. \nObjective: to study the relationship between craving for alcohol, and levels of glycemia and ketonemia in alcoholized rats. \nMaterials and methods. Male white rats (n = 40) were forcibly alcoholized with 10% ethanol in 16 weeks. After that, for 30 days, they had a free choice of three types of drinking: clean water, 5% glucose, and 10% ethanol. The volume of consumed liquids was recorded. The criterion for the developed alcohol dependence was the preference of ethanol. At this stage, the animals were divided into 4 groups. Rats were injected per os with 0.8-1.5 ml of: 1.4% unitiol (3.5 mg / kg) to suppress ketonemia – group 1 (n = 10); 40% starch (1.0 g / kg) to eliminate hypoglycemia – group 2 (n = 10); 2.8% unitiol and 80% starch to suppress ketonemia and eliminate hypoglycemia – group 3 (n = 10); 0.9% NaCl as a control – group 4 (n = 10). Blood glucose (from the tail vein) and urine ketone bodies were monitored. The glucose level was determined with a glucometer. Test strips were used to detect ketone bodies in urine. The results were processed with MedStat software. To measure the strength of the correlation between the indicators, Spearman and Pearson tests were used. \nResults. No ketone bodies were found in the urine of healthy animals; however, after the end of forced alcoholization, varying levels of ketonuria were recorded in all rats: from 0.5 to 10 mmol / L (Spearman's rank correlation test was 0.8). Glycemia in healthy rats was 7.0 ± 1.4 mmol / L. After alcoholization, it decreased (p <0.001) to 3.0 ± 0.7 mmol / l. Ethanol consumption during first 10 days of forced alcoholization was 3.2 ± 0.7 ml per 100 g of animal weight; by the end of the third week - 4.9 ± 1.1 ml; by the end of the sixth week - 6.4 ± 1.4 ml (this was a climax of consumption, since consumption did not increase up to the 16th week). \nAfter a 30-day correction, the level of glycemia (mmol / L) was as follows: animals of the 1st group (unitiol) - 4.0 ± 0.8; animals of the 2nd group (enhanced carbohydrate diet) - 7.1 ± 1.2; animals of the 3rd group (unitiol + enhanced carbohydrate diet) - 7.1 ± 1.1; animals of the 4th group (0.9% NaCl) - 3.5 ± 0.8. \nAlcohol consumption (ml per 100 g of animal weight) after 30-day correction was as follows: in group 1 (unitiol) - 5.1 ± 0.9; in group 2 (enhanced carbohydrate diet) - 2.7 ± 1; in group 3 (unitiol + enhanced carbohydrate diet) - 3.5 ± 1.5; in group 4 (0.9% NaCl) - 4.5 ± 1.2. \nA positive strong correlation was found between ethanol consumption and a decrease in glycemia (Pearson's test – 0.8). \nConclusion. In alcoholized animals with severe hypoglycemia and ketosis, drug suppression of ketosis does not reduce the craving for ethanol. Metabolic correction, aimed at eliminating hypoglycemia, helps to reduce alcohol consumption and reduce the severity of ketosis. The reason for maintaining a stable craving for alcohol is the metabolic demand of the brain for ketone bodies, as alternative food sources in conditions of alcoholic hypoglycemia, and the synthesis of which is stimulated by alcohol intake.","PeriodicalId":52737,"journal":{"name":"Medichna nauka Ukrayini","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medichna nauka Ukrayini","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32345/2664-4738.4.2022.03","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Relevance. In case of developed alcoholic disease, under conditions of alcoholic hypoglycemia, ketone bodies act as an energy substrate for the brain. However, the role of ketone hunger for maintaining the craving for alcohol has not been established. The assumption of such a connection has a right to exist, since it is alcohol that stimulates the formation of ketone bodies. Therefore, with developed alcoholism, the desire to consume alcohol (and, in fact, "saturate" the brain with ketone bodies) can be considered as a consequence of hypoketonemia. Accordingly, the hunger of the alcoholic is the result of hypoketonemia, but not hypoglycemia. Therefore, it is relevant to conduct a study in which the given variables (controlled by us) were the level of glycemia and the level of ketonemia, and the amount of alcohol consumed voluntarily (under conditions of free choice) was a derivative and dependent value. Objective: to study the relationship between craving for alcohol, and levels of glycemia and ketonemia in alcoholized rats. Materials and methods. Male white rats (n = 40) were forcibly alcoholized with 10% ethanol in 16 weeks. After that, for 30 days, they had a free choice of three types of drinking: clean water, 5% glucose, and 10% ethanol. The volume of consumed liquids was recorded. The criterion for the developed alcohol dependence was the preference of ethanol. At this stage, the animals were divided into 4 groups. Rats were injected per os with 0.8-1.5 ml of: 1.4% unitiol (3.5 mg / kg) to suppress ketonemia – group 1 (n = 10); 40% starch (1.0 g / kg) to eliminate hypoglycemia – group 2 (n = 10); 2.8% unitiol and 80% starch to suppress ketonemia and eliminate hypoglycemia – group 3 (n = 10); 0.9% NaCl as a control – group 4 (n = 10). Blood glucose (from the tail vein) and urine ketone bodies were monitored. The glucose level was determined with a glucometer. Test strips were used to detect ketone bodies in urine. The results were processed with MedStat software. To measure the strength of the correlation between the indicators, Spearman and Pearson tests were used. Results. No ketone bodies were found in the urine of healthy animals; however, after the end of forced alcoholization, varying levels of ketonuria were recorded in all rats: from 0.5 to 10 mmol / L (Spearman's rank correlation test was 0.8). Glycemia in healthy rats was 7.0 ± 1.4 mmol / L. After alcoholization, it decreased (p <0.001) to 3.0 ± 0.7 mmol / l. Ethanol consumption during first 10 days of forced alcoholization was 3.2 ± 0.7 ml per 100 g of animal weight; by the end of the third week - 4.9 ± 1.1 ml; by the end of the sixth week - 6.4 ± 1.4 ml (this was a climax of consumption, since consumption did not increase up to the 16th week). After a 30-day correction, the level of glycemia (mmol / L) was as follows: animals of the 1st group (unitiol) - 4.0 ± 0.8; animals of the 2nd group (enhanced carbohydrate diet) - 7.1 ± 1.2; animals of the 3rd group (unitiol + enhanced carbohydrate diet) - 7.1 ± 1.1; animals of the 4th group (0.9% NaCl) - 3.5 ± 0.8. Alcohol consumption (ml per 100 g of animal weight) after 30-day correction was as follows: in group 1 (unitiol) - 5.1 ± 0.9; in group 2 (enhanced carbohydrate diet) - 2.7 ± 1; in group 3 (unitiol + enhanced carbohydrate diet) - 3.5 ± 1.5; in group 4 (0.9% NaCl) - 4.5 ± 1.2. A positive strong correlation was found between ethanol consumption and a decrease in glycemia (Pearson's test – 0.8). Conclusion. In alcoholized animals with severe hypoglycemia and ketosis, drug suppression of ketosis does not reduce the craving for ethanol. Metabolic correction, aimed at eliminating hypoglycemia, helps to reduce alcohol consumption and reduce the severity of ketosis. The reason for maintaining a stable craving for alcohol is the metabolic demand of the brain for ketone bodies, as alternative food sources in conditions of alcoholic hypoglycemia, and the synthesis of which is stimulated by alcohol intake.
酮症和血糖水平对酒精中毒大鼠对乙醇渴望的影响
关联在发生酒精性疾病的情况下,在酒精性低血糖的条件下,酮体充当大脑的能量底物。然而,酮饥饿在维持对酒精的渴望方面的作用尚未确定。这种联系的假设有权存在,因为正是酒精刺激酮体的形成。因此,随着酒精中毒的发展,饮酒的欲望(事实上,酮体使大脑“饱和”)可以被认为是低酮血症的结果。因此,酗酒者的饥饿感是低酮血症的结果,而不是低血糖。因此,进行一项研究是相关的,在该研究中,给定的变量(由我们控制)是血糖水平和酮症酸中毒水平,而自愿饮酒量(在自由选择的条件下)是一个导数和依赖值。目的:探讨酒精中毒大鼠对酒精的渴求与血糖、酮症酸中毒的关系。材料和方法。雄性大鼠(n=40)在16周内用10%乙醇强制醇化。在那之后的30天里,他们可以自由选择三种类型的饮料:干净的水、5%的葡萄糖和10%的乙醇。记录消耗液体的体积。产生酒精依赖性的标准是对乙醇的偏好。在此阶段,将动物分为4组。大鼠经口注射0.8-1.5 ml:1.4%乌尼奥尔(3.5 mg/kg)以抑制酮症酸中毒-第1组(n=10);40%淀粉(1.0 g/kg)消除低血糖-第2组(n=10);2.8%unitiol和80%淀粉抑制酮症酸中毒并消除低血糖症——第3组(n=10);0.9%氯化钠作为对照——第4组(n=10)。监测血糖(来自尾静脉)和尿酮体。用血糖仪测定血糖水平。试纸条用于检测尿液中的酮体。使用MedStat软件对结果进行处理。为了衡量指标之间的相关性,使用了Spearman和Pearson检验。后果在健康动物的尿液中未发现酮体;然而,在强制醇化结束后,所有大鼠都记录到不同水平的丙酮尿症:从0.5到10 mmol/L(Spearman秩相关检验为0.8)。健康大鼠的血糖为7.0±1.4 mmol/L。醇化后,血糖降至3.0±0.7 mmol/L(p<0.001)。强制醇化前10天的乙醇消耗量为每100克动物体重3.2±0.7毫升;第三周结束时为4.9±1.1 ml;到第六周结束时-6.4±1.4毫升(这是消耗量的高潮,因为直到第16周消耗量没有增加)。经过30天的校正后,血糖水平(mmol/L)如下:第一组动物(unitiol)-4.0±0.8;第二组动物(强化碳水化合物饮食)-7.1±1.2;第3组动物(unitiol+强化碳水化合物饮食)-7.1±1.1;第4组动物(0.9%氯化钠)-3.5±0.8。校正30天后的酒精消耗量(ml/100g动物体重)如下:第1组(unitiol)-5.1±0.9;第2组(强化碳水化合物饮食)-2.7±1;第3组(unitiol+强化碳水化合物饮食)-3.5±1.5;第4组(0.9%NaCl)-4.5±1.2。乙醇消耗量与血糖下降之间存在强正相关(Pearson检验–0.8)。结论。在患有严重低血糖和酮症的酗酒者中,药物抑制酮症并不能减少对乙醇的渴望。代谢矫正旨在消除低血糖,有助于减少饮酒量,降低酮症的严重程度。对酒精保持稳定渴望的原因是大脑对酮体的代谢需求,酮体是酒精性低血糖条件下的替代食物来源,其合成受到酒精摄入的刺激。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
24
审稿时长
7 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信