|Year : 2019 | Volume
| Issue : 1 | Page : 33-38
Effects of rosuvastatin on metabolic profile: Versatility of dose-dependent effect
Hayder M Al-Kuraishy, Ali I Al-Gareeb
Department of Pharmacology, Toxicology and Medicine, College of Medicine, Al-Mustansiriya University, Baghdad, Iraq
|Date of Web Publication||12-Feb-2019|
Dr. Hayder M Al-Kuraishy
Department of Pharmacology, Toxicology and Medicine, College of Medicine, Al-Mustansiriya University, P. O. Box 14132, Baghdad
Source of Support: None, Conflict of Interest: None
Obesity refers to an excess of body fat content causing metabolic and inflammatory disorders. Therefore, the aim of the present study was to investigate dose-dependent effect of rosuvastatin on the metabolic profile of diet-induced obesity in mice model study. A total number of 40 male Albino Swiss mice were used which divided into Group I: Control group, fed normal diet for 8 weeks (n = 10); Group II: High-fat diet (HFD) group, fed on HFD for 8 weeks (n = 10); Group III: HFD + 20 mg/kg rosuvastatin for 8 weeks (n = 10); and Group IV: HFD +40 mg/kg rosuvastatin for 8 weeks (n = 10). Anthropometric and biochemical parameters were estimated, including fasting blood glucose, lipid profile, fasting insulin, and glucose tolerance test (GTT). Mice on HFD fed showed a significant increase in the insulin resistance, body weight, deterioration of lipid profile and significant reduction in the β-cell function, and insulin sensitivity compared to the control P < 0.05. GTT and blood glucose level were significantly high in HFD fed group compared to the control group P < 0.05. Rosuvastatin in a dose of 40 mg/kg illustrated better effect than 20 mg/kg on the glucometabolic profile P < 0.05. Rosuvastatin may has a potential effect on reduction of glucometabolic changes induced by HFD with significant amelioration of pancreatic β-cell function in dose-dependent manner.
Keywords: Fasting blood glucose, fasting insulin, glucose tolerance test, insulin tolerance test, lipid profile, obesity, rosuvastatin
|How to cite this article:|
Al-Kuraishy HM, Al-Gareeb AI. Effects of rosuvastatin on metabolic profile: Versatility of dose-dependent effect. J Adv Pharm Technol Res 2019;10:33-8
|How to cite this URL:|
Al-Kuraishy HM, Al-Gareeb AI. Effects of rosuvastatin on metabolic profile: Versatility of dose-dependent effect. J Adv Pharm Technol Res [serial online] 2019 [cited 2020 Nov 29];10:33-8. Available from: https://www.japtr.org/text.asp?2019/10/1/33/252123
| Introduction|| |
Obesity refers to an excess of the body fat content causing metabolic and inflammatory disorders. Large-scale studies have been performed to study the association between obesity with physical and mental health problems. Obesity is linked to metabolic syndrome that is characterized by visceral obesity, insulin resistance (IR), and hypertension.
Body mass index (BMI) was introduced as a valuable tool to assess overweight and obesity. The world health organization used BMI cutoff values to set the classification of obesity in adults.
It is evident that BMI varies with gender, age, and ethnicity; however, it is not considered as a sensitive measure for body fat content but still be considered as the most practical and simple tool in the epidemiological studies. A dose-related increase in body weight and risk of type 2 diabetes mellitus (T2DM) with statin therapy has been recognized.
Similar to other statins, rosuvastatin inhibits the active site of 3-hydroxy-3-methyl-glutaryl-coenzyme. A reductase (HMG-CoA). The efficacy of rosuvastatin is related to the fluorinated phenyl and methyl sulfonamide groups (polar group) which allow multiple affinity and interaction with HMG-CoA reductase enzyme.,
Therefore, the aim of the present study was to investigate the dose-dependent effect of rosuvastatin on the metabolic profile of diet-induced obesity in mice model study.
| Materials and Methods|| |
A total number of 40 male Albino Swiss mice were used with age and weight 2–3 months and 250–300 g, respectively, they kept in sterilized cages at 23°Ċ temperature with 12/12 artificial light-dark cycle. Free access to normal chow and water was allowed, and they left for 1 week of adaptation. All mice were cared for in accordance and harmony with guide for the care and use of laboratory animals. The experimental protocol was approved and reviewed by the Animal Care Review Committee at College of Medicine, Al-Mustansiriyia University.
Drugs and chemicals
High-fat diet (HFD) (60% fat D12492 Research Diets, Inc., New Brunswick, NJ, USA), glucose solution 50% (glucose 50 ml vial, team medical supplies, Phebra, Ray RD), soluble insulin (Actrarapid HM, neutral insulin injection 100 IU/ml, Novo Nordisk, IndiaMART), and rosuvastatin (rosuvastatin STADA 10 mg, IndiaMART) which were purchased from private pharmaceutical company.
After the acclimatization period, the mice were divided into the following:
- Group I: Control group, fed normal diet for 8 weeks (n = 10)
- Group II: HFD group, fed on HFD for 8 weeks (n = 10)
- Group III: Treated group, fed with HFD for 4 weeks and received single daily dose of 20 mg/kg rosuvastatin orally for 4 weeks (n = 10)
- Group IV: Treated group, fed with HFD for 8 weeks and received single daily dose of 40 mg/kg rosuvastatin orally for 4 weeks (n = 10).
Weight measurement, food intake, fasting blood glucose, glucose tolerance test (GTT), insulin tolerance test (ITT), lipid profile measurement, and fasting insulin levels were measured at baseline, 4 weeks, and 8 weeks after induction of obesity.
Measurement of food intake and body weight
The weighed food was poured in the cages and left for 24 h. The remaining food was collected, weighed, and the difference between food weights was calculated that represented the food intake in g/24 h. Measurement of mice weight was done by digital weight calculator.
In addition, glucose tolerance test (GTT) was done according to the previous methods.,
Plasma sample collection
Blood samples were collected after mice decapitation in labeled-EDTA containing tubes. The blood samples were centrifuged at 5000 rpm for 10 min. The supernatant layer was stored at −20°Ċ until the time of analysis.
Serum lipid profile was measured using ELISA kit method. Low-density lipoprotein (LDL) level was calculated according to Lee et al., method. Very LDL (VLDL) = TG/5. Atherogenic Index of Plasma (AIP) was estimated using the equation AIP = log (triglyceride [TG]/HDL-c).,
Fasting insulin level was determined by ELISA kit (Mouse insulin [INS] kit, Shanghai Yehua biological technology, China). Homeostasis model assessment for IR (HOMA-IR) = fasting insulin concentration (μIU/ml) × fasting glucose concentration (mg/dl)/405. HOMA-β = (fasting plasma insulin level [μIU/ml] × 360)/(fasting plasma glucose level [mg/dl]-63). Insulin sensitivity was estimated using the quantitative insulin check index equation: QUICKI = 1/(log (fasting plasma insulin [μIU/ml] + log [fasting plasma glucose [mg/dl]).
Data were expressed as mean ± standard deviation. Students paired and unpaired t-test was used to compare values between baselines and follow-up values. One-way ANOVA test the differences between the groups. All statistical procedures were done by Statistical Package for the Social Sciences (SPSS), version 22.0 (SPSS 22.0, 2016, IBM Corp., NY, USA). P < 0.05 was considered statistically significant.
| Results|| |
Food intake and body weight were increased in HFD compared to the control (P = 0.001). HFD group showed a significant increase in total cholesterol (TC), LDL, and TG sera levels with elevated AIP (P = 0.001), and decrease in HDL-c level (P = 0.001) compared to the control while VLDL serum level was increased in HFD mice compared to the control (P = 0.02). HFD mice showed significant increase in the fasting blood glucose, fasting insulin level compared to the control (P = 0.0001 and P = 0.05), respectively. In addition, HFD mice showed significant increase in the IR with decrease in β-cell function and insulin sensitivity (P < 0.05). GTT and blood glucose level were significantly high in HFD mice compared to the control group (P = 0.001) [Table 1].
Food intake and body weight were high in HFD compared to HFD-rosuvastatin group (P = 0.01) and (P = 0.02), respectively. Body weight was not significant at a dose of 20 mg/kg compared to HFD-rosuvastatin group (P = 0.07). LDL and both TC and TG were high in HFD compared to HFD-rosuvastatin group either at 20 mg/kg or 40 mg/kg (P = 0.001). There was no significant change in HDL levels in the treated groups (P = 0.28). Atherogenic Index was high in HFD (0.428 ± 0.010) group compared to HFD-rosuvastatin 20 mg/kg (0.28 ± 0.011) and (0.22 ± 0.082) in HFD-rosuvastatin 40 mg/kg (P = 0.001). Fasting blood glucose was high in rosuvastatin 20 mg/kg (171.00 ± 24.98 mg/dl) (P = 0.001) and low in rosuvastatin 40 mg/kg (124.71 ± 13.66 mg/dl) compared to HFD mice (P = 0.09). Moreover, there were no significant differences regarding fasting specific insulin, QUICKI, and HOMA-IR between HFD and HFD-rosuvastatin treated groups (P = 0.47, P = 0.66, 0.42), respectively. Besides, insulin sensitivity and β-cell function were improved in rosuvastatin group at 40 mg/kg (P = 0.04) but not in rosuvastatin at 20 mg/kg (P = 0.06) compared to HFD group. GTT was low in HFD group compared to HFD + rosuvastatin at 20 mg/kg (P = 0.03) and high compared to HFD + rosuvastatin at 40 mg/kg (P = 0.0001) [Table 2] and [Figure 1], [Figure 2], [Figure 3].
|Table 2: Metabolic dose-dependent effect of rosuvastatin on high-fat diet-induced weight gain|
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|Figure 1: Dose-dependent effect of rosuvastatin on the insulin resistance compared to high-fat diet and control groups. *P < 0.01 compared to the control, #P = 0.42 compared to high-fat diet, one-way ANOVA test P < 0.01|
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|Figure 2: Dose-dependent effect of rosuvastatin on β-cell function compared to high-fat diet and control groups. *P < 0.01 compared to the control, #P < 0.05 compared to high-fat diet, One-way ANOVA test P < 0.01|
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|Figure 3: Dose-dependent effect of rosuvastatin on the insulin sensitivity compared to high-fat diet and control groups. *P > 0.05 compared to the control, #P > 0.05 compared to high-fat diet, One-way ANOVA test P > 0.05|
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| Discussion|| |
The present study illustrated that intake of HFD for 2 consecutive months increase body weight significantly compared to the control, which coincides with the previous findings.
HFD-induced obesity is linked with the development of central insulin and/or leptin resistance in rodent model within a short duration. Besides, HFD leads to peripheral IR that provokes brain glucose uptake which per se stimulate appetite and food intake.
Fasting insulin and fasting blood glucose were elevated in HFD mice since chronic intake of HFD is associated with significant hyperglycemia and hyperinsulinemia. Moreover, high fatty acid metabolites lead to reduction of glucose uptake. Besides, high glucose level stimulates the adaptive response of β-cell through insulin overproduction to compensate the IR.,
In the present study, HFD led to significant glucose intolerance and impaired glucose disposal causing hyperglycemia due to the link between IR and dyslipidemia. As well, IR induces hepatic lipogenesis and hyperinsulinemia which accelerate de novo TG and VLDL synthesis.,
The present study exposed a significant increment in HOMA-IR and the decrement in HOMA-β, QUICKI values within 8 weeks of HFD due to the development of IR and deterioration in β-cell function. These findings correspond with Wanchai et al., a study that illustrated HFD leads to IR and reduction of insulin sensitivity.
Rosuvastatin in the current study led to a significant reduction of body weight since rosuvastatin may affects the satiety. Seif et al. study confirmed that rosuvastatin could counteract the effect of fatty acids on leptin receptors at the hypothalamus.,
Indeed, rosuvastatin illustrated a dose-dependent effect in the improvement of lipid profile and Atherogenic Index suggesting that rosuvastatin may alleviate the bad influence of HFD on lipid metabolism.
As blood glucose elevated, it triggers the release of insulin in response to fasting hyperglycemia in HFD; however, this mechanism is impaired in rosuvastatin-treated group.
It has been reported that chronic depletion of cellular cholesterol in response to rosuvastatin-mediated inhibition of membrane fluidity/rigidity ratio might affects insulin carrier granules attachment to the lipid raft. This finding might explain the potential effect of rosuvastatin on the insulin levels in the present study.
Besides, results of the present study revealed that rosuvastatin improved insulin sensitivity in a dose-dependent manner as 40 mg/kg rosuvastatin led to the improvement of IR with reduction in the insulin release due to the inhibition of gluconeogenesis through the modulation of peroxisome proliferative-activated receptor-γ coactivator-1 (PGC-1α) pathway.,
The exact molecular mechanism of rosuvastatin effect on the β-cell is linked to membrane disorganization or isoprenoids inhibition, disturbed calcium current, and impaired β-cell mitochondrial ATP production. Therefore, rosuvastatin illustrated a dose-dependent effect in the amelioration of pancreatic β-cell during HFD-induced metabolic disturbances, unlike other statins types.
The present study revealed several limitations which are small sample size, short duration of rosuvastatin effect, lack the values of blood pressure measurement, and obesity-linked inflammatory biomarkers. However, this study may be regarded as a preliminary study for large-scale human study to assess the beneficial effect of rosuvastatin in patients with T2DM and associated overweight and/or metabolic syndrome.
| Conclusion|| |
Rosuvastatin may has a potential effect on reduction of glucometabolic changes induced by HFD with significant amelioration of pancreatic β-cell function in dose-dependent manner.
The author would like to acknowledge Pr. Dr. Saddiq Al-Hamash Head of Al-Mustansiriyia in Iraq.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Al-Gareeb AI, Aljubory KD, Alkuraishy HM. Niclosamide as an anti-obesity drug: An experimental study. Eat Weight Disord 2017;22:339-44.
Al-Kuraishy HM, Al-Gareeb AI. Effects of rosuvastatin alone or in combination with omega-3 fatty acid on adiponectin levels and cardiometabolic profile. J Basic Clin Pharm 2016;8:8-14.
Kêkê LM, Samouda H, Jacobs J, di Pompeo C, Lemdani M, Hubert H, et al.
Body mass index and childhood obesity classification systems: A comparison of the French, International Obesity Task Force (IOTF) and World Health Organization (WHO) references. Rev Epidemiol Sante Publique 2015;63:173-82.
Al-Kuraishy HM, Al-Gareeb AI. Effect of orlistat alone or in combination with Garcinia cambogia
on visceral adiposity index in obese patients. J Intercult Ethnopharmacol 2016;5:408-14.
Al-Naimi MS, Hussien NR, Rasheed HA, Al-Kuraishy HM, Al-Gareeb AI. Levothyroxine improves Paraoxonase (PON-1) serum levels in patients with primary hypothyroidism: Case–control study. Journal of advanced pharmaceutical technology & research 2018;9(3):113.
Al-Kuraishy HM, Al-Gareeb AI, Al-Buhadilly AK. Rosuvastatin improves vaspin serum levels in obese patients with acute coronary syndrome. Diseases 2018;6. pii: E9.
Zhao W, Zhao SP. Different effects of statins on induction of diabetes mellitus: An experimental study. Drug Des Devel Ther 2015;9:6211-23.
The National Academies Collection: Reports funded by National Institutes of Health, National Research Council (US) Committee for the Update of the Guide for the Care and Use of Laboratory Animals. In: Guide for the Care and Use of Laboratory Animals. 8th
ed. Washington (DC): National Academies Press (US); 2011.
Coelho AR, Moreira FA, Santos AC, Silva-Pinto A, Sarmento A, Carvalho D, et al.
Diabetes mellitus in HIV-infected patients: Fasting glucose, A1c, or oral glucose tolerance test – Which method to choose for the diagnosis? BMC Infect Dis 2018;18:309.
di Iorgi N, Napoli F, Allegri A, Secco A, Calandra E, Calcagno A, et al.
The accuracy of the glucagon test compared to the insulin tolerance test in the diagnosis of adrenal insufficiency in young children with growth hormone deficiency. J Clin Endocrinol Metab 2010;95:2132-9.
Lee J, Jang S, Jeong H, Ryu OH. Validation of the Friedewald formula for estimating low-density lipoprotein cholesterol: The Korea National Health and Nutrition Examination Survey, 2009 to 2011. Korean J Intern Med 2018;21.
Al-Kuraishy HM, Al-Gareeb AI. Acylation-stimulating protein is a surrogate biomarker for acute myocardial infarction: Role of statins. J Lab Physicians 2017;9:163-9.
] [Full text]
Ouyang F, Christoffel KK, Brickman WJ, Zimmerman D, Wang B, Xing H, et al.
Adiposity is inversely related to insulin sensitivity in relatively lean Chinese adolescents: A population-based twin study. Am J Clin Nutr 2010;91:662-71.
Penaforte FR, Japur CC, Diez-Garcia RW, Chiarello PG. Effects of a high-fat meal on postprandial incretin responses, appetite scores and ad libitum
energy intake in women with obesity. Nutr Hosp 2017;34:376-82.
Ahangarpour A, Alboghobeish S, Rezaei M, Khodayar MJ, Oroojan AA, Zainvand M, et al.
Evaluation of diabetogenic mechanism of high-fat diet in combination with arsenic exposure in male mice. Iran J Pharm Res 2018;17:164-83.
Yan Z, Shyr ZA, Fortunato M, Welscher A, Alisio M, Martino M, et al.
High-fat-diet-induced remission of diabetes in a subset of KATP – GOF insulin-secretory-deficient mice. Diabetes Obes Metab 2018;20:2574-84.
Hao YR, Tang FJ, Zhang X, Wang H. Suppression of NF-κB activation by PDLIM2 restrains hepatic lipogenesis and inflammation in high fat diet induced mice. Biochem Biophys Res Commun 2018;503:564-71.
Soares GM, Zangerolamo L, Azevedo EG, Costa-Júnior JM, Carneiro EM, Saad ST, et al.
Whole body ARHGAP21 reduction improves glucose homeostasis in high-fat diet obese mice. J Cell Physiol 2018;233:7112-9.
Wilfred DC, Mysorekar VV, Venkataramana RS, Eshwarappa M, Subramanyan R. Nondiabetic renal disease in type 2 diabetes mellitus patients: A Clinicopathological study. J Lab Physicians 2013;5:94-9.
] [Full text]
Arnold SE, Lucki I, Brookshire BR, Carlson GC, Browne CA, Kazi H, et al.
High fat diet produces brain insulin resistance, synaptodendritic abnormalities and altered behavior in mice. Neurobiol Dis 2014;67:79-87.
Wanchai K, Yasom S, Tunapong W, Chunchai T, Eaimworawuthikul S, Thiennimitr P, et al.
Probiotic Lactobacillus paracasei
HII01 protects rats against obese-insulin resistance-induced kidney injury and impaired renal organic anion transporter 3 function. Clin Sci (Lond) 2018;132:1545-63.
Han W, Li J, Tang H, Sun L. Treatment of obese asthma in a mouse model by simvastatin is associated with improving dyslipidemia and decreasing leptin level. Biochem Biophys Res Commun 2017;484:396-402.
Seif El-Din SH, El-Lakkany NM, El-Naggar AA, Hammam OA, Abd El-Latif HA, Ain-Shoka AA, et al.
Effects of rosuvastatin and/or β-carotene on non-alcoholic fatty liver in rats. Res Pharm Sci 2015;10:275-87.
Ahmadi Y, Haghjoo AG, Dastmalchi S, Nemati M, Bargahi N. Effects of rosuvastatin on the expression of the genes involved in cholesterol metabolism in rats: Adaptive responses by extrahepatic tissues. Gene 2018;661:45-50.
Salunkhe VA, Elvstam O, Eliasson L, Wendt A. Rosuvastatin treatment affects both basal and glucose-induced insulin secretion in INS-1 832/13 cells. PLoS One 2016;11:e0151592.
Muscogiuri G, Sarno G, Gastaldelli A, Savastano S, Ascione A, Colao A, et al.
The good and bad effects of statins on insulin sensitivity and secretion. Endocr Res 2014;39:137-43.
Koh KK, Oh PC, Sakuma I, Lee Y, Han SH, Shin EK, et al.
Rosuvastatin dose-dependently improves flow-mediated dilation, but reduces adiponectin levels and insulin sensitivity in hypercholesterolemic patients. Int J Cardiol 2016;223:488-93.
Alkuraishy HM, Al-Gareeb AI, Waheed HJ. Lipoprotein-Associated phospholipase A2 is linked with poor cardio-metabolic profile in patients with ischemic stroke: A study of effects of statins. Journal of neurosciences in rural practice 2018;9(4):496.
Al-Kuraishy HM, Al-Gareeb AI, Al-Buhadily AK. Rosuvastatin as forthcoming antibiotic or as adjuvant additive agent: In vitro
novel antibacterial study. Journal of laboratory physicians 2018;10(3):271.
Urbano F, Bugliani M, Filippello A, Scamporrino A, Di Mauro S, Di Pino A, et al.
Atorvastatin but not pravastatin impairs mitochondrial function in human pancreatic islets and rat β-cells. Direct effect of oxidative stress. Sci Rep 2017;7:11863.
[Figure 1], [Figure 2], [Figure 3]
[Table 1], [Table 2]
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