دورية أكاديمية

Influence of 10-(6-plastoquinonyl) decyltriphenylphosphonium on free-radical homeostasis in the heart and blood serum of rats with streptozotocin-induced hyperglycemia.

التفاصيل البيبلوغرافية
العنوان: Influence of 10-(6-plastoquinonyl) decyltriphenylphosphonium on free-radical homeostasis in the heart and blood serum of rats with streptozotocin-induced hyperglycemia.
المؤلفون: Agarkov AA; Department of Medical Biochemistry and Microbiology, Voronezh State University, Voronezh 394018, Russia. agalalek@mail.ru., Popova TN; Department of Medical Biochemistry and Microbiology, Voronezh State University, Voronezh 394018, Russia., Boltysheva YG; Department of Medical Biochemistry and Microbiology, Voronezh State University, Voronezh 394018, Russia.
المصدر: World journal of diabetes [World J Diabetes] 2019 Dec 15; Vol. 10 (12), pp. 546-559.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Baishideng Publishing Group Country of Publication: United States NLM ID: 101547524 Publication Model: Print Cited Medium: Print ISSN: 1948-9358 (Print) Linking ISSN: 19489358 NLM ISO Abbreviation: World J Diabetes Subsets: PubMed not MEDLINE
أسماء مطبوعة: Publication: 2014-: Pleasanton, CA : Baishideng Publishing Group
Original Publication: Beijing, China : Beijing Baishideng BioMed Scientifc Company
مستخلص: Background: It is known that under conditions of tissue tolerance to insulin, observed during type 2 diabetes mellitus (DM2), there is an increased production of reactive oxygen species. Moreover, the free radicals can initiate lipid peroxidation (LPO) in lipoprotein particles. The concentration of LPO products can influence the state of insulin receptors, repressing their hormone connection activity, which is expressed as a reduction of the glucose consumption by cells. It is possible that reduction in glucose concentration during administration of 10-(6-plastoquinonyl) decyltriphenylphosphonium (SkQ1) to rats with DM2 may be related to the antioxidant properties of this substance.
Aim: To establish the influence of SkQ1 on free-radical homeostasis in the heart and blood serum of rats with streptozotocin-induced hyperglycemia.
Methods: To induce hyperglycemia, rats were fed a high-fat diet for 1 mo and then administered two intra-abdominal injections of streptozotocin with a 7-d interval at a 30 mg/kg of animal weight dose with citrate buffer equal to pH 4.4. SkQ1 solution was administered intraperitoneally at a 1250 nmol/kg dose per day. Tissue samples were taken from control animals, animals with experimental hyperglycemia, rats with streptozotocin-induced glycemia that were administered SkQ1 solution, animals housed under standard vivarium conditions that were administered SkQ1, rats that were administered intraperitoneally citrate buffer equal to pH 4.4 once a week during 2 wk after 1-mo high-fat diet, and animals that were administered intraperitoneally with appropriate amount of solution without SkQ1 (98% ethanol diluted eight times with normal saline solution). To determine the intensity of free radical oxidation and total antioxidant activity, we used the biochemiluminescence method. Aconitate hydratase (AH), superoxide dismutase, and catalase activities were estimated using the Hitachi U-1900 spectrophotometer supplied with software. The amount of citrate was determined by means of the Natelson method. Real-time polymerase chain reaction was carried out using an amplifier ANK-32.
Results: It was found that the mitochondrial-directed antioxidant elicits decrease of biochemiluminescence parameter values that increase by pathology as well as the levels of primary products of LPO, such as diene conjugates and carbonyl compounds, which indicate intensity of free radical oxidation. At the same time, the activity of AH, considered a crucial target of free radicals, which decreased during experimental hyperglycemia, increased. Apparently, increasing activity of AH influenced the speed of citrate utilization, whose concentration decreased after administering SkQ1 by pathology. Moreover, the previously applied anti-oxidant during hyperglycemia influenced the rate of antioxidant system mobilization. Thus, superoxide dismutase and catalase activity, as well as the level of gene transcript under influence of SkQ1 at pathology, were changing to the direction of control groups values.
Conclusion: According to the results of performed research, SkQ1 can be considered a promising addition to be included in antioxidant therapy of DM2.
Competing Interests: Conflict-of-interest statement: Potential conflicts of interest not detected.
(©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved.)
References: Diabetes. 2000 Nov;49(11):1939-45. (PMID: 11078463)
J Ophthalmol. 2014;2014:530943. (PMID: 25132985)
Nature. 2001 Dec 13;414(6865):813-20. (PMID: 11742414)
Nat Rev Endocrinol. 2016 Mar;12(3):144-53. (PMID: 26678809)
Nature. 2002 Sep 19;419(6904):316-21. (PMID: 12239572)
J Neurosci. 2004 Aug 18;24(33):7324-34. (PMID: 15317858)
Circulation. 2004 May 11;109(18):2191-6. (PMID: 15123530)
Clin Chim Acta. 1991 Feb 15;196(2-3):143-51. (PMID: 2029780)
Kardiologiia. 2009;49(10):55-60. (PMID: 19845521)
Oncogene. 2006 Oct 30;25(51):6706-16. (PMID: 17072323)
Int J Biochem Cell Biol. 2018 Apr;97:98-103. (PMID: 29454114)
Biochemistry (Mosc). 2008 Dec;73(12):1273-87. (PMID: 19120014)
Methods Enzymol. 1994;233:357-63. (PMID: 8015470)
Antioxid Redox Signal. 2011 Feb 15;14(4):593-605. (PMID: 20618067)
Circulation. 2007 Jun 26;115(25):3213-23. (PMID: 17592090)
Nature. 1966 Jun 11;210(5041):1162-3. (PMID: 4960496)
Trends Biochem Sci. 2014 Apr;39(4):199-218. (PMID: 24647116)
Aging (Albany NY). 2015 Jul;7(7):475-85. (PMID: 26187706)
Acta Naturae. 2013 Oct;5(4):118-22. (PMID: 24455191)
Pharmacol Res. 2005 Oct;52(4):313-20. (PMID: 15979893)
Science. 2002 Mar 29;295(5564):2450-2. (PMID: 11884717)
Free Radic Biol Med. 1991;11(2):161-8. (PMID: 1937134)
EMBO J. 2004 Dec 8;23(24):4802-12. (PMID: 15538382)
Biochemistry (Mosc). 2008 Sep;73(9):957-64. (PMID: 18976211)
Exp Diabetes Res. 2008;2008:704045. (PMID: 19132099)
Biochemistry (Mosc). 2015 Dec;80(12):1606-13. (PMID: 26638686)
Lab Delo. 1973;2:115-6. (PMID: 4128330)
فهرسة مساهمة: Keywords: 10-(6-plastoquinonyl) decyltriphenylphosphonium; Antioxidants; Diabetes mellitus; Free radical oxidation
تواريخ الأحداث: Date Created: 20200110 Latest Revision: 20201001
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC6944529
DOI: 10.4239/wjd.v10.i12.546
PMID: 31915517
قاعدة البيانات: MEDLINE
الوصف
تدمد:1948-9358
DOI:10.4239/wjd.v10.i12.546