scholarly journals PO-023 The Effects of Aerobic Exercise on Alternative Splicing of PKC δI pre-mRNA

2018 ◽  
Vol 1 (3) ◽  
Author(s):  
Junzhen Shi ◽  
Jinfeng Zhao ◽  
Xuyang Bai ◽  
Baoai Wu
Keyword(s):  
Adipose Tissue ◽  
Alternative Splicing ◽  
Aerobic Exercise ◽  
Low Density Lipoprotein ◽  
Density Lipoprotein ◽  
Exercise Group ◽  
Lipoprotein Cholesterol ◽  
Rt Pcr ◽  
Oil Red O Staining ◽  
Oil Red O

Objective Alternative splicing of genes is the main way to produce large numbers of proteins, but the mechanism is unclear. The aim of this study was to evaluated the effect of aerobic exercise on PKC δI pre-mRNA alternative splicing. Further, to explore the effect of aerobic exercise on SFRS10 concentration. Because the PKCδ1 is involved in the regulation of adipocyte differentiation and splice factor SFRS10 regulates alternative of PKCδ1, explore the mechanism of PKCδ1 alternative splicing, understand the role of the alternative splicing variants, to provide the theory basis for the mechanism of aerobic exercise reduce the incidence of obesity. Methods C57BL/6 male mice were randomly divided into normal quiet group, normal exercise group, obese and quiet group, and obese exercise group. The exercise group performed aerobic exercise for 8 weeks. The intensity of aerobic exercise was: running platform slope is 0, speed 10 m/min, 1 h/time, 1 time/day, 6 times/week for a total of 8 weeks. Immediately after exercise, the cDNA was extracted from liver and adipose tissue. The contents of PKCδ1 and SFRS10 in liver and adipose tissue were determined by PCR and RT-PCR. Liver and fat were stained by oil red O staining to observe lipid droplet changes. And the mouse's Lee's index and blood lipids were determined. Results  Lee's index = 3√ (body weight * 1000) / body length, Lee's index of obese mice decreased significantly after aerobic exercise, in addition, after aerobic exercise, total cholesterol (TC), triglyceride (TG) and low density Lipoprotein cholesterol (LDL-C) also showed a downward trend (P < 0.05), while high-density lipoprotein cholesterol (HDL-C) increased (P < 0.05); oil red O staining results showed lipid droplets become smaller after aerobic exercise. The results of PCR and RT-PCR showed in the obese and quiet group than in the normal quiet group, the content of PKCδ1-FL decreased, the content of PKCδ1-△Exon9 increased, and the content of SFRS10 decreased. In the normal exercise group than in the normal quiet group and in the obese exercise group than in the obese and quiet group, the PKCδ1-FL content increased, the PKCδ1-△Exon9 content decreased, and the SFRS10 content increased. Conclusions  Aerobic exercise can significantly increase the content of PKCδ1-FL and SFRS10. PKCδ1-FL inhibits the formation of adipocytes, SFRS10 promotes the inclusion of PKCδ1 exon 9, and there is a molecular mechanism of alternative splicing between PKCδ1 and SFRS10.

scholarly journals Anti-Obesity Effect of Galacto-Oligosaccharides in Obese Rats

2021 ◽  
Author(s):  
Shang Kong ◽  
Xingjun Huang ◽  
Hua Cao ◽  
Yan Bai ◽  
Qishi Che ◽  
...  
Keyword(s):  
Adipose Tissue ◽  
Fat Body ◽  
Low Density Lipoprotein ◽  
Density Lipoprotein ◽  
Protective Role ◽  
Lipoprotein Cholesterol ◽  
Fat Cells ◽  
Expression Levels ◽  
Brown Adipose ◽  
Obese Rats

Abstract Background: Galacto-oligosaccharides (GOS) is a commonly used as a prebiotic with a variety of metabolic benefits. Whether GOS plays a protective role in obesity is still unknown. Here we demonstrated that GOS possesses an anti-obesity activity by promoting adipose tissue browning and thermogenesis. Results: Our results showed that GOS effectively slow weight gain of diet-induced obese (DIO) rats without affecting energy intake. GOS significantly suppressed the hypertrophy and hyperplasia of white adipose tissue (WAT), as well as markedly lessened the ratio of fat pad to fat body. Consistently, GOS significantly improved serum total cholesterol (TC), triglycerides (TG), high-density lipoprotein cholesterol (HDL-C) and low-density lipoprotein cholesterol (LDL-C) levels, which indicated an appropriate weight loss activity of GOS. Interestingly, GOS also significantly increased the expression levels of browning proteins (UCP1, PPARγ, PGC1α and PRMD16) both in the WAT and brown adipose tissue (BAT). We further found that GOS markedly increased the expression levels of LXRα, PPARα, LDLR and CYP7A1 proteins in the liver of obese rats. Conclusions: Taken together, we concluded that GOS inhibits obesity by accelerating the browning of white fat cells and the thermogenesis of brown fat cells, moreover GOS improves host lipid homeostasis by promoting cholesterol catabolism.

Effect of the Joint Administration of Selenium and Vitamin E in Combination with Regular Aerobic Exercise on Markers of Lipid Peroxidation and Glutathione Peroxidase in Diabetic Rats

2005 ◽  
Vol 15 (3) ◽  
pp. 266-278 ◽  
Author(s):  
Hyun-Tae Kim
Keyword(s):  
Vitamin E ◽  
Exercise Training ◽  
Aerobic Exercise ◽  
Low Density Lipoprotein ◽  
Density Lipoprotein ◽  
Acute Effect ◽  
Exercise Group ◽  
Diabetic Rats ◽  
Aerobic Exercise Training ◽  
Long Term Treatment

We investigated the effect of long-term treatment (6 wk) with selenium and vitamin E, in combination with aerobic exercise training, on malondialdehyde (MDA), oxidized low-density lipoprotein (ox-LDL), and glutathione peroxi-dase (GPx) in STZ-induced diabetic rats. The rats were assigned randomly to one of three treatment groups (n = 12 per group): 1) exercise group (EX), 2) selenium/vitamin E/exercise group (SVE), and 3) selenium/vitamin E group (SV). To estimate the acute effect of exercise, a 30-min endurance exercise was used. The MDA concentration was significantly lower in the SVE. The ox-LDL was significantly lower in the SVE and SV. The hepatic concentrations of selenium and vitamin E were significantly higher in the SVE. These results indicate that the increase in MDA is mildly attenuated in rats that were aerobically trained. Moreover, the joint administration of selenium and vitamin E with or without exercise training reduces the levels of ox-LDL.

scholarly journals PO-021 The Effect of Aerobic Exercise on Alternative Splicing of Lipin1 pre-mRNA and its isoforms

2018 ◽  
Vol 1 (3) ◽  
Author(s):  
Xuyang Bai ◽  
Baoai Wu ◽  
Junzhen Shi ◽  
Infeng Zhao
Keyword(s):  
Alternative Splicing ◽  
Aerobic Exercise ◽  
Exercise Group ◽  
Control Group ◽  
Mrna Levels ◽  
Rt Pcr ◽  
Metabolic Complications ◽  
Obesity Control ◽  
And Control ◽  
Control Exercise

Objective Obesity is one of a world-wide chronic diseases, which is the leading cause of cancer, T2D, cardiovascular disease other metabolic complications. Aerobic exercise as a moderate intervention, has potential mechanisms for the loss weight. Lipin1 as a key regulator of lipid metabolism is a member of the Lipin family. Through alternative splicing, Lipin1 exists two isoforms,Lipin1α is mostly expressed in preadipocytes during the initial stages of differentiation, whereas the Lipin1β mainly expressed in mature adipocytes, and is responsible for lipogenesis and adipocyte hypertrophy.The aim of our present study was to investigate the effect of aerobic exercise on the levels of Lipin1α、Lipin1β and splicing factor SFRS10. Methods C57BL/6 mice were randomly assigned to control group(C, n=20) and obesity control group (O, n=20). After 4weeks,mice were further assigned to normal control group (NC,n=10),and control exercise group (CE,n=10),O group ( O, n = 10) and obesity exercise group (OE, n = 10),CE and OE were on aerobic exercised for 8 weeks. RT-PCR was generated to detect Lipin1α、Lipin1βand SFRS10 mRNA expression. Results The results suggest that the level of lipin1α mRNA was decreased in obesity group. With exercise, levels in CE and OE increased. Furthermore, Lipin1β was increased in obesity group and decrease after aerobic exercise in both CE and OE. We also demonstrated the SFRS10, which can bind to lipin1 exon8 and regulate Lipin1 alternative splicing, had a lower ex pression in obesity group and higher expression in CE and OE.  Conclusions  Our data suggest that aerobic exercise can reduce body weight by influencing lipin1 pre-mRAN alternative splicing, and change the expression of two isoforms. Besides aerobic exercise can also affect SFRS10 mRNA Levels and change the expression of Lipin1 isoform.

scholarly journals Therapeutic potential of small extracellular vesicles derived from lipoma tissue in adipose tissue regeneration—an in vitro and in vivo study

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Pengyu Hong ◽  
Xiaoyang Xu ◽  
Xin Hu ◽  
Hao Yang ◽  
Yue Wu ◽  
...  
Keyword(s):  
Adipose Tissue ◽  
Extracellular Vesicles ◽  
Tissue Regeneration ◽  
Lipid Droplets ◽  
Adipogenic Differentiation ◽  
Rt Pcr ◽  
Oil Red O Staining ◽  
Oil Red O

Abstract Objective To explore the adipogenic effects of the small extracellular vesicles derived from the lipoma tissues (sEV-LT), and to find a new cell-free therapeutic approach for adipose tissue regeneration. Methods Adipose tissue-derived stem cells (ADSCs) and small extracellular vesicles derived from the adipose tissues (sEV-AT) were isolated from human adipose tissue, while sEV-LT were isolated from human lipomatous tissue. ADSCs were characterized by using flow cytometric analysis and adipogenic and osteogenic differentiation assays. sEV was identified by electron microscopy, nanoparticle tracking, and western blotting. ADSCs were treated with sEV-LT and sEV-AT, respectively. Fluorescence confocal microscopy was used to investigate whether sEV-LT and sEV-AT could be taken by ADSCs. The proliferation and migration abilities and adipogenic differentiation assay of ADSCs were evaluated by CCK-8 assays, scratch test, and oil red O staining test, and the expression levels of adipogenic-related genes C/EBP-δ, PPARγ2, and Adiponectin in ADSCs were assessed by real-time quantitative PCR (RT-PCR). The sEV-LT and sEV-AT transplantation tubes were implanted subcutaneously in SD rats, and the neotissues were qualitatively and histologically evaluated at 2, 4, 8, and 12 weeks after transplantation. Hematoxylin and eosin (H&E) staining was subsequently used to observe and compare the adipogenesis and angiogenesis in neotissues, while immunohistochemistry was used to examine the expression and the distribution of C/EBP-α, PPARγ, Adiponectin, and CD31 at the 4th week. Results The in vitro experiments showed that both sEV-LT and sEV-AT could be taken up by ADSCs via endocytosis. The scratch experiment and CCK-8 experiment showed that the migration area and proliferation number of ADSCs in sEV-LT group and sEV-AT group were significantly higher than those in the non-sEV group (p < 0.05). Compared with sEV-AT group, sEV-LT group had larger migration area and proliferation number of ADSCs (p < 0.05). Oil red O staining and RT-PCR experiments showed that, compared with the non-sEVs group, the lipid droplets and the mRNA expression levels of adipogenesis-related genes PPARγ2 and Adiponectin of ADSCs in sEV-LT group and sEV-AT group were significantly upregulated (p < 0.05); however, there was no statistical significance in the expression level of C/EBP-δ (p > 0.05). In addition, no significant difference in the amount of lipid droplets and adipogenesis-related genes between the sEV-LT groups and sEV-AT was seen (p > 0.05). At 2, 4, 8, and 12 weeks, the adipocyte area and the number of capillaries in neotissues in the sEV-LT groups and sEV-AT groups were significantly increased compared with the Matrigel group (p < 0.05); however, there was no dramatic difference between sEV-LT groups and sEV-AT groups (p > 0.05). At the 4th week, neotissues in the sEV-LT groups and sEV-AT groups all showed upregulated expression of C/EBP-α, PPARγ, Adiponectin, and CD31 protein, while neotissues in the Matrigel group only showed positive expression of CD31 protein. Conclusions This study demonstrated that sEV-LT exerted promotion effects on adipose tissue regeneration by accelerating the proliferation, migration, and adipogenic differentiation of ADSCs in vitro and recruiting adipocytes and promoting angiogenesis in vivo. The sEV-LT could serve as an alternative cell-free therapeutic strategy for generating adipose tissue, thus providing a promising application prospect in tissue engineering.

Circulating Omentin-1, Insulin Resistance and Lipid Profile Responses Following 8-weeks Aerobic Training Intervention Among Smokers Vs. Non-smokers

2020 ◽  
Author(s):  
Seyed Maysam Mousavi ◽  
Ali Heidarianpour ◽  
Hassan Tavassoli
Keyword(s):  
Insulin Resistance ◽  
Exercise Training ◽  
Aerobic Exercise ◽  
Lipid Profile ◽  
Density Lipoprotein ◽  
Exercise Group ◽  
Normal Weight ◽  
Aerobic Exercise Training ◽  
Lipoprotein Cholesterol ◽  
Control Group

Abstract Background: Omentin-1 is a recently circulating adipokine that plays a crucial role in modulating insulin resistance and diabetes. We investigated the effect of eight weeks aerobic exercise training on serum omentin-1, insulin resistance and lipid profile in the smoker and non-smokers with normal-weight. Methods: Nineteen healthy men and twenty smoker men were randomly assigned into healthy control group (C), healthy exercise group (E), control smoker group (CS) and exercise smoker group (ES). Exercise groups participated in an 8-weeks aerobic exercise training program (three times a week, 45 min per session at 65%-80% of maximum heart rate). Serum omentin-1 and insulin values were determined by ELISA and HOMA-IR, glucose and lipid profile were measured at pre and post of the intervention. Paired Sample t-test, one-way analysis of variance (One-way ANOVA) and post-hoc Tukey test were applied to analyze the data (p<0.05).Results: Aerobic exercise improved both serum omentin-1 and high lipoprotein cholesterol (HDL-C) in the exercise groups (p<0.05). Also, Exercise training reduced insulin, blood sugar, HOMA-IR, total cholesterol (TC) and low-density lipoprotein cholesterol (LDL-C) levels (p<0.05). Omentin-1 were significantly associated with insulin (r=-0.40, P=0.01), HOMA-IR (r=-0.38, P=0.04), TG (r=-0.40, P=0.01), TC (r=-0.49, P=0.02), LDL-C (r=-0.70, P=0.02) and HDL-C (r=0.55, P=0.03).Conclusion: The findings suggest that aerobic exercise-induced changes in omentin-1 in exercise trained smokers may be associated with the beneficial effects of exercise on reduced insulin and lipid profile.

scholarly journals LOX-1, the Common Therapeutic Target in Hypercholesterolemia: A New Perspective of Antiatherosclerotic Action of Aegeline

2019 ◽  
Vol 2019 ◽  
pp. 1-11 ◽  
Author(s):  
Abhilasha Singh ◽  
Ashok Kumar Srinivasan ◽  
Lakshmi Narasimhan Chakrapani ◽  
Periandavan Kalaiselvi
Keyword(s):  
Histopathological Examination ◽  
Low Density Lipoprotein ◽  
Density Lipoprotein ◽  
High Cholesterol Diet ◽  
Diagnostic Strategy ◽  
Low Density ◽  
Oxidized Low Density Lipoprotein ◽  
Oil Red O Staining ◽  
Oil Red O

Background. Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1) is the major receptor for oxidized low-density lipoprotein (Ox-LDL) in the aorta of aged rats. Ox-LDL initiates LOX-1 activation in the endothelium of lipid-accumulating sites of both animal and human subjects of hypercholesterolemia. Targeting LOX-1 may provide a novel diagnostic strategy towards hypercholesterolemia and vascular diseases. Hypothesis. This study was planned to address whether aegeline (AG) could bind to LOX-1 with a higher affinity and modulate the uptake of Ox-LDL in hypercholesterolemia. Study Design. Thirty-six Wistar rats were divided into six groups. The pathology group rats were fed with high-cholesterol diet (HCD) for 45 days, and the treatment group rats were fed with HCD and aegeline/atorvastatin (AV) for the last 30 days. In vivo and in vitro experiments were carried out to assay the markers of atherosclerosis like Ox-LDL and LOX-1 levels. Histopathological examination was performed. Oil Red O staining was carried out in the IC-21 cell line. Docking studies were performed. Results. AG administration effectively brought down the lipid levels induced by HCD. The lowered levels of Ox-LDL and LOX-1 in AG-administered rats deem it to be a potent antihypercholesterolemic agent. Compared to AV, AG had a pronounced effect in downregulating the expression of lipids evidenced by Oil Red O staining. AG binds with LOX-1 at a higher affinity validated by docking. Conclusion. This study validates AG to be an effective stratagem in bringing down the lipid stress induced by HCD and can be deemed as an antihypercholesterolemic agent.

Adipocytes‐secreted hormone leptin, lipid profile and aerobic exercise program

2012 ◽  
Vol 1 (6) ◽  
pp. 292-297
Author(s):  
Eizadi Mojtaba ◽  
Kohandel Mahdi ◽  
Kasbparast JR Mehdi ◽  
Sarshin Amir
Keyword(s):  
Exercise Training ◽  
Aerobic Exercise ◽  
Lipid Profile ◽  
Exercise Program ◽  
Density Lipoprotein ◽  
Exercise Group ◽  
Lipoprotein Cholesterol ◽  
Control Group ◽  
Blood Samples ◽  
And Control

The adipocyte‐derived hormones leptin is known to increase in obesity and related disease. Thirty two non‐trained males (39±4.32 years, 176.5 – 6.5 ± 6.42 cm, and 31 ± 3.14 body fat %) were matched according to physical fitness enrolled in this study and divided to exercise and control group by accidentally. The participants of exercise group were completed an aerobic exercise program for 3 months (3 days/weekly) and control group were barred of exercise in this period. Anthropometrical measurements and fasting blood samples were obtained before and after interventions in two groups. Blood samples were collected in order to measuring serum leptin, triglyceride (TG), high density lipoprotein cholesterol (HDL), and Low density lipoprotein cholesterol (LDL). Pre‐ and post exercise independent variables were compared using a paired‐samples t‐test. Compared to pre‐training, the leptin levels decreased significantly (P<0.01) after aerobic exercise program in exercise group but not in the control subjects. Triglyceride concentration was decreased with exercise training whereas concentrations of LDL cholesterol did not change in exercise group (p≥0.05). Exercise training resulted in significant decrease in anthropometrical indexes (p Ë‚ 0.05) and a borderline significant increase in HDL (p=0.052). TG/HDL ratio were significantly decreased in exercise group by exercise training (p=0.028). All variable in control group remained no change in control group (p ≥ 0.05). These data suggest, despite lack significant changes in some lipid profile markers, aerobic exercise program can be improve systemic inflammation and TG/HDL ratio as a cardiovascular risk factor in obese subjects.

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