CC BY
30
□dû* International Journal of Endocrinology
OpuriHOAbHi AOOAÏA^eHHq
/Original Researches/
UDC 616.379-008.64-021.6 DOI: https://doi.Org/10.22141/2224-0721.16.8.2020.222878
M. Bostani , S.A. Noaein
Department of Physical Education, Ahvaz Branch, Islamic Azad University, Ahvaz, Iran
Physical activity as a non-pharmacological and useful strategy in controlling of the apoptotic symptoms in diabetic model rats
For citation: Miznarodnij endokrinobgicnij zurnal. 2020;16(8):602-606. doi: 10.22141/2224-0721.16.8.2020.222878
Abstract. Background. In recent years, diabetes has become a global health problem. Apoptosis of pancreatic beta cells plays an important role in the pathogenesis of type 1 diabetes. Exercise as a non-pharmacological strategy to reduce the diabetic-induced complications has always been of interest to researchers. Therefore, the purpose of this study was to investigate the effect of aerobic exercise on levels of Bax, Bcl-2 and Bax/Bcl-2 ratio in pancreatic tissue of streptozotocin (STZ)-induced diabetic rats. Materials and methods. A total number of 40 male Wistar rats (10 weeks old, 200-250 gr weight) were randomly divided into healthy control (HC), healthy trained (HT), diabetic control (DC), and diabetic trained (DT) groups. Diabetes was also induced by a single in-traperitoneally injection of streptozocin (45 mg/kg). The training groups performed the exercise on the treadmill for five consecutive days within six weeks. The pancreatic tissue levels of the Bax and the Bcl-2 proteins were further determined via ELISA method. Results. The results showed that the induction of diabetes had significantly decreased the levels of Bcl-2 protein and increased the levels of Bax protein and Bax/Bcl-2 ratio in the pancreatic tissue (p < 0.05). As well, the findings showed that six weeks of aerobic exercise training had significantly increased the levels of Bcl-2 and significantly decreased the levels of Bax protein in DT group. Also, the Bax/Bcl-2 ratio reduced significantly in DT group (p < 0.05). The increase in displacement and transmission of apoptosis inducing factor (AIF) that have seen in oxidative stress status, is reduced in the tissues of trained individuals which indicating of the inhibition in the apoptotic signaling. Conclusions. According to the results of this study, exercise can be considered as an effective strategy to reduce the rate of diabetic-induced apoptosis and control its complications. Keywords: exercise; Bax; Bcl-2; apoptosis; diabetes mellitus
Introduction
Diabetes mellitus (DM) is a chronic metabolic disorder of the endocrine glands that has affected millions of people around the world and often associated with the functional and structural complications in various organs [1]. Pancreatic beta cell apoptosis plays an important role in the pathogenesis and development of Type 1 Diabetes mellitus (T1DM) [2, 3]. Mitochondrial apoptosis pathway involves the loss of mitochondrial homeostasis especially changes in the outer mitochondrial membrane. Mitochondrial outer membrane dysfunction causes proliferation of proapoptosis factors including cytochrome c. The release of cytochrome c activates the apoptosome. After the formation of this apoptosome and especially the activation of caspase 9, other important caspa-ses are activated. Eventually, apoptosis culminates in cell
death [4, 5]. Bax and Bcl-2 are two important proteins that involved in the process of apoptosis through the formation of the apoptosome complex as well as the activator and inhibitor of caspases. Bax/Bcl-2 ratio is known to determine the survival and death of the cell [6]. The Bcl-2 family proteins play a vital role in transmission of intracellular apoptotic signals by regulating the permeability of the mitochondrial membrane. These proteins are divided into two categories: Anti-apopto-tic proteins such as Bcl-2 and pro-apoptotic proteins such as Bax [7]. Bcl-2 is attached to the outer mitochondrial membrane and can inhibit the release of cytochrome c to cysto-sol, while the Bax protein damage the outer membrane of the mitochondria and cause the release of cytochrome c to the cytosol. It is also well established that the Bax protein can be attached to the Bcl-2 and prevent its anti-apoptotic role [8].
© 2020. The Authors. This is an open access article under the terms of the Creative Commons Attribution 4.0 International License, CC BY, which allows others to freely distribute the published article, with the obligatory reference to the authors of original works and original publication in this journal.
For correspondence: Mehdi Bostani, PhD, Department of Physical Education, Ahvaz Branch, Islamic Azad University, Ahvaz, Iran; e-mail: Bostanim@yahoo.com; contact phone: +989167017668 Full list of author information is available at the end of the article.
Exercise and physical activities have been recommended for the decrease of complications in in patients with diabetes [9—11]. Cheng et al. [12] in their study showed that exercise training with increases the levels of Bcl-2 protein, enhances the cell survival in the heart of diabetic mice. N. Ramezani et al. [13] in their study reported that high-intensity interval training It caused a significant increase in Bcl-2 and decreased significantly in Bax after the four-week training intervention in heart of diabetic rats.
According to various studies, the effect of physical activity on apoptotic factors in diabetic pancreatic tissue has not been studied, therefore the aim of this study was to examine the levels of Bax protein, Bcl-2 protein and Bax/Bcl-2 ratio and studying the effect of aerobic exercise training in pancreas tissue of streptozotocin (STZ)-induced diabetic rats.
Materials and methods Animals
A total number of 40 adult male Wistar rats were supplied from Razi Institute (Karaj, Iran) and housed four-per-cage in an animal lab under standard conditions (12-hour light/ dark cycle in a room at a temperature of 20—25 °C) with access to food and water ad libitum. All the institutional (as registered under the code LUNS.REC.1395.170 at Lorestan University of Medical Sciences) and animal research health guidelines were also observed. The animals were randomly divided into four groups: 1) healthy control (HC, N = 10); 2) healthy trained (HT, N = 10); 3) diabetic control (DC, N = 10), and 4) diabetic trained (DT, N = 10) followed by inducing diabetes in DT and DC groups.
Diabetes induction
For the purpose of acclimatization and reaching optimal weight (at least 250 gr), all of the rats were kept in an animal lab for two weeks prior to the experiments. Subsequently, following an overnight fasting, diabetes was induced through a single intraperitoneal injection of streptozotocin (STZ) (45 mg/kg; Sigma, St. Louis, MO) solution (dissolved in 0.5 mol/l citrate buffer at pH 4.0). Two days later, diabetes was confirmed through measuring tail vein blood glucose level (> 350 mg/ld.) by Accu-Chek Compact Plus blood glucometer (Roche Diagnostics K.K., Tokyo, Japan). In this respect, the animals without any trace of hypergly-cemic were excluded from the rest of the samples. In addition, blood glucose levels were controlled all along the study course, once every week [29].
Treadmill training protocol
The treadmill training protocol was developed based on previous protocols which consisted of 6 weeks of moderate-intensity endurance aerobic exercise on a leveled motor-driven treadmill (Model T510E, Diagnostic and Research, Taoyuan, Taiwan). The aerobic power of the animals in terms of V02max was further obtained based on the rela-
tionship between V02max to speed and treadmill slope [14]. Within the first week, the speed and the duration of the treadmill running were 10 m/min and 10 min per day, respectively. The figures were then gradually increased until the fifth week, ending up with training speed and duration of 18 m/min and 30 min per day, respectively. To stabilize the obtained adaptations, training speed and duration were kept constant at the sixth week [15].
Tissue extraction
Two days after the last exercise session in the sixth week of training, the animals were anesthetized by inhalation of 2 % halothane in a mixture of 20 % O2 and 80 % CO2. For the analysis of the levels of Bax and the Bcl-2 pancreatic tissue, total rats in four-groups were removed immediately and separated pancreatic tissue were stored at —80 °C until the analysis process was completed.
Evaluation of Bax and Bcl-2
To measure the expression of the Bax and the Bcl-2 proteins, the ELISA kits were used (Cusabio-Japan). At the first step, the Bax and the Bcl-2 levels of the pancreatic were homogenized (1 : 10 in PBS 10 Mm, pH 7.4 in 4 °C) and then centrifuged (20,000 rpm in 45 min). After that, using special kits of rats (Bax; 15.6 pg/ml and Bcl-2; 0.078 pg/ml), the levels of proteins were measured and spectrophotometri-cally read by an Autobio Elisa Reader (China).
Statistical analysis
Statistical analyses were conducted using SPSS Statistics software (Version 21, SPSS Inc., Chicago, IL, USA). Normality and homogeneity of the data were also assessed via Sha-piro-Wilk test and Levene's test, respectively. One-way analysis of variance (ANOVA) followed by Bonferroni post-hoc test was further employed to compare the Bax and the Bcl-2 levels in the HC, HT, DC, and DT groups. The data were reported as mean ± standard error of measurement (SEM) values and the statistical significance level was set by p < 0.05.
Results
Figure 1 illustrated the average of blood glucose levels during the six-week endurance training intervention in the diabetic groups. As shown, blood glucose levels within six weeks in the diabetic group were more than 300 mg/dl which was considered as the threshold for diabetes. In the diabetic control group, the blood glucose levels had been also rising since the injection of the STZ by the end of the sixth week; but in the diabetic trained group, a decreasing trend was observed which revealed a significant reduction started at the beginning of the fourth week of the study (p < 0.05).
As shown in Figure 2, the levels of the Bax protein in the DC group significantly increased compared to the HC group (p < 0.05). There was also a significant reduction in Bcl-2 protein levels in the diabetic control (DC) group com-
Table 1. Endurance Training Protocol
First week Second week Third week Forth week Fifth week Sixth week
Training duration (minute) 10 20 20 30 30 30
Treadmill speed (m/min) 10 10 15 15 18 18
pared to the healthy group (HC). Also, the Bax/Bcl-2 ratio in the diabetic rats increased significantly (p < 0.05).
In the diabetic group that performed aerobic exercise on a treadmill for six weeks, there was a significant decrease in the levels of Bax protein, significant increase in Bcl-2 protein and significant reduction in the Bax/Bcl-2 ratio compared to the diabetic control group (p < 0.05).
Discussion
In the present study, we found that in the streptozoto-cin (STZ)-induced diabetic rats, the levels of the Bax pro-apoptotic protein increased, but the levels of the Bcl-2 anti-apoptotic protein decreased. In addition, Bax/Bcl-2 ratio was increased also. This means that pro-apoptosis processes have overcome anti-apoptosis processes in diabetic pancreas tissue.
However, six-weeks of aerobic exercise led to an increase in Bcl-2 anti-apoptosis protein and a decrease in the Bax pro-apoptosis protein and the Bax/Bcl-2 ratio.
The mechanism of the relationship between cell death and hyperglycemia is not yet well understood. Diabetes-induced oxidative stress may play an important role in the development of apoptosis in hyperglycemic state. Oxidative stress is created by an imbalance between the production of reactive oxygen species (ROS) and antioxidant factors. The role of the free radicals in the dysfunction of beta cells has been well established, in fact increment of the oxidative stress plays an important role in the spread of diabetic-induced cell death in most tissues [16, 17]. It is believed that the oxidative stress to be a major factor of the adverse effects of diabetes on tissues, which can trigger or accelerate apoptosis in affected cells [18].
The results of the various studies have shown that physical activity can reduce the amount and speed of cellular apoptosis. Some of these studies have suggested that the mechanism of the reduction in cellular death related to the increase in body's antioxidant capacity [19], reduction in the cytokines such as TNF-a [20], the decrease in the levels of pre-apoptotic proteins such as Bax protein [21], increasing the anti-apoptotic factors (Bcl-2, Hsp70), increasing the some of DNA regeneration enzymes and reduction in ROS production [22]. It seems that the mitochondria play an essential role in regulating of the apoptotic events. in this regard, the members of Bcl-2 family, including Bax
700-1
n
ra 600-
£
m 500-
<l>
> CD 400-
(1)
</) O 300-
O
~Ül 200-
TD
O O 100-
m
0
H=H
* i i
DC DT
48 hour First Second Third Forth Fifth Sixth week week week week week week
Weeks of training
Figure 1. Blood glucose levels during the six weeks Note: * — P < 0.05 significant decrease in blood glucose levels in diabetic trained (DT) versus the diabetic control (DC) group.
and Bcl-2 proteins as the main proteins, are involved in the formation of apoptotic channels, mitochondrial permeability regulation, and mitochondrial apoptosis signaling [23]. The Bax/Bcl-2 ratio is also an indicator for the determine of the mitochondrial apoptosis potential, which Bcl-2 through preventing of Bax-Bax oligomerization, opposes the pro-apoptotic activity of Bax. As soon as the Bax protein enters to mitochondria, it forms the pores in the mitochondrial membrane, that results in the release of proteins such as cy-tochrome C into the cystosol and triggers the downstream apoptotic signaling caspase cascade such as caspases-3 and caspases-9 [24]. The importance of the mitochondrial permeability has been explained in the J. Fang et al. study in 2008. They showed that the blocking of the mitochondrial permeability pores reduces the rate of apoptosis [25]. Moreover, the Bcl-2 protein by entering the mitochondrial outer membrane, maintains the integrity of the membrane and through the removing of H ions from the ion channels and via binding to apaf-1, inhibits caspase activation [26, 27].
In response to exercise, the levels of oxidative stress are associated with the less phosphorylation of c-Jun-N-termi-nal kinase (JNK). This is accompanied by a reduction in the expression of Bax protein and its transfer to mitochondria, as well as an increase in the levels of Bcl-2 protein.
Figure 2. Diabetes decreased the levels of the Bcl-2 protein and increased the Bax protein in the pancreatic tissue, while aerobic exercise training for six weeks significantly increased the Bcl-2 and decreased the Bax protein
Note: * — Significantly different, p < 0.01.
Figure 3. Diabetes increased the Bax/Bcl-2 ratio in the pancreatic tissue, however aerobic exercise training for six weeks significantly decreased this ratio
Note: * — Significantly different, p < 0.01.
In addition, the increase in displacement and transmission of apoptosis inducing factor (AIF) that have seen in oxidative stress status, is reduced in the tissues of trained individuals which indicating of the inhibition in the apoptotic signaling [28, 29].
Conclusions
According to the results of the present study, it can be concluded that aerobic exercise as a non-pharmacological, low-cost and useful strategy can be considered by reducing the levels of pro-apoptosis and increasing the amounts of anti-apoptosis factors, and can control diabetes-induced cell death and its complications.
Acknowledgements
This manuscript is derived from the master's thesis of Islamic Azad University, Ahvaz Branch, Iran. Therefore, the author et al. thanks the mentioned university.
Conflicts of interests. Authors declare the absence of any conflicts of interests and their own financial interest that might be construed to influence the results or interpretation of their manuscript.
References
1. Zhao L, Gu Q, Xiang L, et al. Curcumin inhibits apoptosis by modulating Bax/Bcl-2 expression and alleviates oxidative stress in testes of streptozotocin-induced diabetic rats. Ther Clin Risk Manag. 2017Aug 28;13:1099-1105. doi:10.2147/TCRM.S141738.
2. Atkinson MA. ADA Outstanding Scientific Achievement Lecture 2004. Thirty years of investigating the autoimmune basis for type 1 diabetes: why can't we prevent or reverse this disease? Diabetes. 2005May;54(5):1253-1263. doi:10.2337/diabetes.54.5.1253.
3. Kim KA, Lee MS. Recent progress in research on beta-cell apoptosis by cytokines. Front Biosci (Landmark Ed). 2009 Jan 1;14:657-664. doi:10.2741/3271.
4. Kroemer G, Galluzzi L, Brenner C. Mitochondrial membrane permeabilization in cell death. Physiol Rev. 2007 Jan;87(1):99-163. doi:10.1152/physrev. 00013.2006.
5. Susnow N, Zeng L, Margineantu D, Hockenbery DM. Bcl-2 family proteins as regulators of oxidative stress. Semin Cancer Biol. 2009Feb;19(1):42-49. doi:10.1016/j.semcancer.2008.12.002.
6. Raisova M, Hossini AM, et al. The Bax/Bcl-2 ratio determines the susceptibility of human melanoma cells to CD95/Fas-mediated apoptosis. J Invest Dermatol. 2001 Aug; 117(2):333-340. doi:10.1046/j.0022-202x.2001.01409.x.
7. Youle RJ, Strasser A. The BCL-2 protein family: opposing activities that mediate cell death. Nat Rev Mol Cell Biol. 2008 Jan;9(1):47-59. doi:10.1038/nrm2308.
8. Wattenberg B, Lithgow T. Targeting of C-terminal (tail)-anchored proteins: understanding how cytoplasmic activities are anchored to intracellular membranes. Traffic. 2001 Jan;2(l):66-71. doi:10.1034/j.1600-0854.2001.20108.x.
9. Asa C, Maria S, Katharina SS, Bert A. Aquatic exercise is effective in improving exercise performance in patients with heart failure and type 2 diabetes mellitus. EvidBased Complement Alternat Med. 2012;2012:349209. doi:10.1155/2012/349209.
10. Selagzi H, Buyukakilli B, Cimen B, Yilmaz N, Erdogan S. Protective and therapeutic effects of swimming exercise training on
diabetic peripheral neuropathy of .streptozotocin-induced diabetic rats. J Endocrinol Invest. 2008 Nov;31(ll):971-978. doi:10.1007/ BF03345634.
11. Kadoglou NP, Vrabas IS, Kapelouzou A, et al. The impact of aerobic exercise training on novel adipokines, apelin and ghrelin, in patients with type 2 diabetes. Med Sci Monit. 2012 May;18(5):CR290-5. doi:10.12659/msm.882734.
12. Cheng SM, Ho TJ, Yang AL, et al. Exercise training enhances cardiac IGFI-R/PI3K/Akt and Bcl-2 family associated pro-survival pathways in streptozotocin-induced diabetic rats. Int J Cardiol. 2013 Jul 31;167(2):478-485. doi:10.1016/j.ijcard.2012.01.031.
13. Vsdna Nagesh S, Muniappan M, Kannan I, Viswanathan S. Erratum for Nagesh et al., phytochemical analysis and docking study of compounds present in a polyherbal preparation used in the treatment of dermatophytosis. Curr MedMycol. 2018 Mar;4(1):34. doi:10.18502/cmm.4.1.33.
14. Hoydal MA, Wisloff U, Kemi OJ, Ellingsen O. Running speed and maximal oxygen uptake in rats and mice: practical implications for exercise training. Eur J Cardiovasc Prev Rehabil. 2007 Dec;14(6):753-760. doi:10.1097/HJR.0b013e3281eacef1.
15. Chae CH, Jung SL, An SH, et al. Treadmill exercise improves cognitive function and facilitates nerve growth factor signaling by activating mitogen-activated protein kinase/extracellular signal-regulated kinase1/2 in the streptozotocin-induced diabetic rat hippocampus. Neuroscience. 2009 Dec 29; 164(4): 1665-1673. doi: 10.1016/j. neuroscience.2009.09.075.
16. Devine PJ, Perreault SD, Luderer U. Roles of reactive oxygen species and antioxidants in ovarian toxicity. Biol Reprod. 2012 Feb 9;86(2):27. doi:10.1095/biolreprod.111.095224.
17. Agarwal A, Aponte-Mellado A, Premkumar BJ, Shaman A, Gupta S. The effects of oxidative stress on female reproduction: a review. ReprodBiolEndocrinol. 2012 Jun 29;10:49. doi:10.1186/1477-7827-10-49.
18. Nayki U, Onk D, Balci G, Nayki C, Onk A, Gunay M. The Effects of Diabetes Mellitus on Ovarian Injury and Reserve: An Experimental Study. Gynecol Obstet Invest. 2016;81(5):424-429. doi:10.1159/000442287.
19. Gomez-Cabrera MC, Viña J, Ji LL. Interplay of oxi-dants and antioxidants during exercise: implications for muscle health. Phys Sportsmed. 2009 Dec;37(4): 116-123. doi:10.3810/ psm.2009.12.1749.
20. Batista ML Jr, Rosa JC, Lopes RD, et al. Exercise training changes IL-10/TNF-alpha ratio in the skeletal muscle of post-MI rats. Cytokine. 2010 Jan;49(1):102-108. doi:10.1016/j.cyto.2009.10.007.
21. Siu PM, BrynerRW, Martyn JK, Alway SE. Apoptotic adaptations from exercise training in skeletal and cardiac muscles. FASEB J. 2004 Jul;18(10):1150-1152. doi:10.1096/fj.03-1291fje.
22. Fisher-Wellman K, Bloomer RJ. Acute exercise and oxidative stress: a 30 year history. Dyn Med. 2009 Jan 13;8:1. doi:10.1186/1476-5918-8-1.
23. Dejean LM, Martinez-Caballero S, Manon S, Kinnally KW. Regulation of the mitochondrial apoptosis-induced channel, MAC, by BCL-2 family proteins. BiochimBiophys Acta. 2006Feb;1762(2):191-201. doi:10.1016/j.bbadis.2005.07.002.
24. Peterson JM, Bryner RW, Sindler A, Frisbee JC, Alway SE. Mitochondrial apoptotic signaling is elevated in cardiac but not skeletal muscle in the obese Zucker rat and is reduced with aerobic exercise. J Appl Physiol (1985). 2008 Dec; 105(6): 1934-1943. doi:10.1152/japplphysiol.00037.2008.
25. Fang J, Wu L, Chen L. Postconditioning attenuates cardio-
cyte ultrastructure injury and apoptosis by blocking mitochondrial permeability transition in rats. Acta Cardiol. 2008 Jun;63(3):377-387. doi:10.2143/AC.63.3.1020316.
26. Garcia-Saez AJ. The .secrets of the Bcl-2 family. Cell Death Differ. 2012Nov;19(11):1733-1740. doi:10.1038/cdd.2012.105.
27. Kwak HB. Effects of aging and exercise training on apoptosis in the heart. J Exerc Rehabil. 2013 Apr; 9(2): 212-219. doi:10.12965/jer.130002.
28. Vainshtein A, Kazak L, Hood DA. Effects of endurance training on apoptotic susceptibility in striated muscle. J Appl Physiol (1985). 2011 Jun; 110(6): 1638-1645. doi: 10.1152/japplphysi-
ol.00020.2011.
29. Bostani M, Rahmati M, Mard SA. The effect of endurance training on levels ofLINC complex proteins in skeletal muscle fibers of STZ-induced diabetic rats. Sci Rep. 2020 May 26; 10(1):8738. doi:10.1038/s41598-020-65793-5.
Received 09.11.2020 Revised 03.12.2020 Accepted 10.12.2020 ■
Information about authors
Mehdi Bostani, PhD, Department of Physical Education, Ahvaz Branch, Islamic Azad University, Ahvaz, Iran; https://orcid.org/0000-0002-4904-0690 Seyed Aenollah Noaein, Department of Physical Education, Ahvaz Branch, Islamic Azad University, Ahvaz, Iran
Bostani M., Noaein S.A.
Department of Physical Education, Ahvaz Branch, Islamic Azad University, Ahvaz, Iran
$i3MMHO OKTMBHicTb ak He^apMaKOAoriMHa TO e$eKTMBHO crpaTerifl B KOHTpoAi cuMnTOMiB anonT03y y ^ypiB 3 eKcnepMMeHTaAbHMM gia6eTOM
Резюме. Актуальтсть. За останш роки цукровий дiабет (ЦД) став глобальною проблемою охорони здоров'я. Апоп-тоз бета-клиин шдшлунково! залози вщграе важливу роль у патогенезi ЦД 1-го типу. Фiзична актившсть як нефармако-логiчна стратег1я для зменшення частоти ускладнень, спри-чинених ЦД, завжди цiкавила дослщниюв. Тому метою цього дослщження було встановлення впливу аеробних вправ на рiвнi Вах, Вс1-2 та Вах/Вс1-2 у тканиш пхдшлунково! залози стрептозоцин-iнIдукованих дiабетичних щурiв. Матерiали та методи. Самщв щурiв лiнii "Маг (вiком 10 тижшв, вага 200— 250 г) загальною ильюстю 40 ранIдомiзовано розподшили на групи здорового контролю (ЗК), здорових тренованих (ЗТ), з дiабетом (контроль, ДК) та з дiабетом iз фiзичним наван-таженням (ДН). Дiабет був iнIдукований одноразовою штра-перитонеальною iн'eкцieю стрептозоцину (45 мг/кг). Трену-вальнi групи виконували вправу на бгговш дорiжцi п'ять дшв посп1ль протягом шести тижнiв. Рiвнi тканин пщшлунково!
залози в бшках Вах та Вс1-2 додатково визначали методом 1ФА. Результати. Iндукцiя дiабету суттево знизила рiвень бiлка Вс1-2 та зб1льшила р1вень б1лка Вах та сшввщношення Вах/Вс1-2 у тканиш пiдшлунковоi залози (р < 0,05). О^м того, результати показали, що ш1сть тижнiв аеробних трену-вань значно пщвищили рiвень бiлка Вс1-2 та знизили рiвень бiлка Вах у груш ДН. Також сшввщношення Вах/Вс1-2 суттево знизилось у груш ДН (р < 0,05). Посилення видшення та передачi фактора, що шдукуе апоптоз, який спостерггаеться в станi окислювального стресу, зменшуеться в тканинах тренованих ошб, що вказуе на гальмування в сигнатзаци апоптозу. Висновки. Згщно з результатами цього дослщження, фiзичнi вправи можна розглядати як ефективну стратегш зменшення частоти спричиненого дiабетом апоптозу та контролю його ускладнень.
Ключовi слова: фiзичнi вправи; Вах; Вс1-2; апоптоз; цукровий дiабет
Bostani M., Noaein S.A.
Department of Physical Education, Ahvaz Branch, Islamic Azad University, Ahvaz, Iran
Физическая активность как нефармакологическая и эффективная стратегия в контроле симптомов апоптоза у крыс с экспериментальным диабетом
Резюме. Актуальность. За последние годы сахарный диабет (СД) стал глобальной проблемой здравоохранения. Апоптоз бета-клеток поджелудочной железы играет важную роль в патогенезе СД 1-го типа. Физическая активность как нефармакологическая стратегия для уменьшения частоты осложнений, вызванных диабетом, всегда интересовала исследователей. Поэтому целью данного исследования было установление влияния аэробных упражнений на уровни Вах, Вс1-2 и Вах/Вс1-2 в ткани поджелудочной железы стрепто-зоцин-индуцированных диабетических крыс. Материалы и методы. Самцы крыс линии "Маг (в возрасте 10 недель, вес 200—250 г), общее количество 40, были рандомизированы на группы здорового контроля (ЗК), здоровых тренированных (ЗТ), с диабетом (контроль, ДК) и с диабетом с физической нагрузкой (ДН). Диабет был индуцирован однократной ин-траперитонеальной инъекцией стрептозоцина (45 мг/кг). Тренировочные группы выполняли упражнения на беговой дорожке пять дней подряд в течение шести недель. Уровни
тканей поджелудочной железы в белках Вах и Вс1-2 дополнительно определяли методом ИФА. Результаты. Индукция диабета существенно снизила уровень белка Вс1-2 и увеличила уровень белка Вах и соотношение Вах/Вс1-2 в ткани поджелудочной железы (р < 0,05). Кроме того, результаты показали, что шесть недель аэробных тренировок значительно повысили уровень белка Вс1-2 и снизили уровень белка Вах в группе ДН. Также соотношение Вах/Вс1-2 существенно снизилось в группе ДН (р < 0,05). Усиление выделения и передачи фактора, индуцирующего апоптоз, который наблюдается в состоянии окислительного стресса, уменьшается в тканях тренированных лиц и указывает на торможение в сигнализации апоптоза. Выводы. Согласно результатам этого исследования, физические упражнения можно рассматривать как эффективную стратегию уменьшения частоты апоптоза, вызванного диабетом, и контроля его осложнений. Ключевые слова: физические упражнения; Вах; Вс1-2; апоптоз; сахарный диабет
