Molecular and immunohistochemical effects of metformin in a rat model of type 2 diabetes mellitus
- Authors:
- Published online on: March 13, 2015 https://doi.org/10.3892/etm.2015.2354
- Pages: 1921-1930
Abstract
Introduction
In 2010, 285 million individuals were estimated to have been diagnosed with diabetes mellitus worldwide, a prevalence of 6.4%, which is predicted to increase to 439 million (7.7%) by 2030 (1). The mortality rate of diabetes mellitus, including indirect mortalities, is estimated to be ∼3.96 million per year for all age groups, which is a prevalence of 6.8% (2). Type 2 diabetes mellitus (T2DM) accounts for ∼90% of diabetes cases worldwide (1). T2DM has been described as a ʻsilent diseaseʼ (3) and is characterized by a combination of inadequate insulin secretion due to islet β cell deterioration and insulin resistance (IR) (3). Interruption of pancreatic β cell function and insulin activity characterizes T2DM, resulting in symptoms which include dyslipidemia, hyperglycemia, hypertension and atherosclerosis, which subsequently contribute to reduced insulin sensitivity (4).
T2DM is associated with IR, which induces a range of detrimental effects in various organs and tissues. The impact of IR on the central nervous system (CNS) may lead to obesity, as the appetite may be enhanced as a result of the activity of insulin in the CNS (5). In adipose tissue, IR causes hyperlipidemia. Under normal conditions, insulin promotes adipocyte differentiation and glucose uptake, while inhibiting lipolysis in adipocytes. Furthermore, adipose tissue is able to function as an endocrine organ by releasing cytokines and hormones, a function which is disrupted by fat expansion, thus promoting IR (6). In pancreatic tissue, IR impairs β cell regeneration (7). However, whether insulin has a direct autocrine function on β cells in promoting insulin secretion is yet to be fully elucidated (8).
Jung et al (9) identified a novel hepatokine secreted by the liver, named fetuin-A, which was found to be associated with obesity, IR and non-alcoholic fatty liver disease. Fetuin-A affects insulin signal transduction by inhibiting the activity of the insulin receptor tyrosine kinase in the liver and skeletal muscle, in addition to mitigating insulin receptor autophosphorylation in vitro and in vivo, subsequently resulting in IR (10). An additional novel biological marker that can function as a reliable indicator of IR is retinol binding protein-4 (RBP-4). RBP-4 may serve crucial functions in the development of IR and atherosclerosis in T2DM patients with coronary artery disease. Further study of these marker proteins and peptides may aid in the diagnosis and alleviation of IR (11). Perilipins are a family of proteins that target the surfaces of lipid droplets to regulate lipid storage and hydrolysis. A previous study investigating perilipin activity indicated the physiological function of cytosolic lipid droplets and their association with obesity-associated diseases, such as IR (12).
Metformin hydrochloride is one of the most commonly used treatments for T2DM. Metformin improves insulin sensitivity, reduces gluconeogenesis, promotes glucose uptake and reduces glucose production in the liver (13,14). In combination with lifestyle modifications, metformin is the primary glucose-lowering agent used in the treatment of T2DM, due to its efficacy, safety and beneficial cardiovascular and metabolic activity (15,16). Notably, metformin exerts pleiotropic effects in a number of tissues that are affected by IR and hyperinsulinemia, such as skeletal muscles, adipose tissue and the endothelium (17). Although metformin has been used in clinical practice for >40 years, the exact underlying mechanism of action is yet to be fully elucidated (18).
The present study investigated the effects of metformin on dyslipidemia and the expression of genes associated with lipid metabolism in T2DM rats. The effects of metformin were assessed at a molecular and immunohistopathological level.
Materials and methods
Reagents
Streptozotocin (STZ) and metformin were purchased from Sigma-Aldrich (St. Louis, MO, USA). Wistar albino rats were purchased from Egyptian Co. for Experimental Animals Production (Helwan, Egypt). Solvents and associated reagents were purchased from ADWIA Pharmaceuticals (Obour City, Egypt). The high-fat diet (HFD) was purchased from Qaha Co. for Food Production (Qaha, Egypt). Biochemical kits to assess the lipids profiles were obtained from Clini Lab (Heliopolis, Egypt).
Induction of T2DM and experimental design
In total, 30 male Wistar rats (age, 4 weeks; weight, 80–100 g) were selected at random. The rats were exposed to a 12-h day/night cycle, with free access to food and water. The present study was approved by the Ethics Committee on Animal Care of Taif University (Taif, Saudi Arabia; project no. #3103/1435/1). Rats were divided into three groups (n=10 per group). Control group rats received a normal diet. In order to induce IR and T2DM, the remaining 20 rats received a HFD for 4 weeks, which consisted of 15.5% protein, 38.8% fat and 45.7% carbohydrates, by calories. Induction of T2DM in the HFD-fed rats was based on the protocol outlined by Srinivasan et al (19), which comprised an intraperitoneal injection of STZ (35 mg/kg body weight), followed by administration of the HFD for 4 weeks. T2DM was confirmed after 1 week, as serum glucose levels and lipid profiles were increased. The T2DM rats (n=20) were subsequently divided into two subgroups, namely the T2DM group (n=10) and the T2DM + metformin group (n=10), in which metformin (400 mg/kg/day) was administered for 4 weeks.
Following the experimental procedures, all rats were decapitated following inhalation of diethyl ether and after overnight fasting and blood samples were collected for serum extraction and serum chemistry analysis. In addition, liver and adipose tissues were maintained in TRIzol reagent (Invitrogen Life Technologies, Carlsbad, CA, USA) for RNA extraction and semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR) analysis of gene expression.
Serum chemistry analysis
Levels of serum triglycerides (TG), total cholesterol (TC), low-density lipoproteins (LDLs), very low-density lipoproteins (VLDLs) and high-density lipoproteins (HDLs) were measured using commercial spectrophotometric analysis kits. Insulin and glucose levels were measured using spectrophotometric commercial kits. All the kits were purchased from Bio-Diagnostic Company (Giza, Egypt).
cDNA synthesis, semi-quantitative RT-PCR analysis and gene expression
Liver and epididymal adipose tissues were collected from rats, flash frozen in 1 ml TRIzol reagent and subsequently stored at −70°C. Frozen samples (∼100 mg tissue per sample) were immediately homogenized using a POLYTRON 300 D homogenizer (Brinkmann Instruments, Inc., Westbury, NY, USA). Total RNA was extracted via chloroform extraction, which was followed by nucleic acid precipitation with isopropanol. The pellet was washed with 75% ethanol and resuspended in molecular biology grade water. The nucleic acid concentration was measured at an optical density of 260 nm using a SmartSpec spectrophotometer (Bio-Rad Laboratories, Inc., Hercules, CA, USA). The RNA integrity was evaluated using an Agilent 2100 Bioanalyzer (Agilent Technologies, Inc., Foster City, CA, USA).
RNA (1 µg) was treated at 70°C for 5 min and reverse transcribed using 100 units Moloney Murine Leukemia Virus Reverse Transcriptase (Gibco Life Technologies, Carlsbad, CA, USA), 50 pmol poly (dT) primer and 20 nmol dNTPs, in a total volume of 10 µl at 37°C for 1 h. After heating at 94°C for 5 min, PCR amplification was performed using 2.5 units Taq polymerase (PerkinElmer, Inc., Waltham, MA, USA), 3 mM MgCl2 and 50 pmol forward and reverse primers specific for the respective genes, in a total volume of 25 µl. The PCR conditions for the various genes investigated are presented in Table I. PCR products were visualized under an ultra-violet lamp following electrophoresis in 1.5% agarose gel stained with ethidium bromide. Intensities of the PCR bands were analyzed densitometrically using ImageJ software (version 1.48; http://imagej.en.softonic.com).
Liver and pancreatic histopathology and immunohistochemistry
Rats were anesthetized with diethyl ether and the liver was incised. Following removal of the liver from the rats, the liver was fixed overnight in 10% buffered neutral formalin solution. Fixed tissues were processed routinely by washing, dehydration, clearing, paraffin embedding, casting and sectioning into 5-µm slices for hematoxylin and eosin staining (20). With regard to immunohistochemistry, pancreatic tissue sections were deparaffinized and treated with 3% H2O2 for 10 min to inactivate the peroxidases. Subsequently, the tissue samples were heated in 10 mM citrate buffer at 121°C for 30 min for antigen retrieval, blocked in 5% normal serum for 20 min, and incubated with a rabbit polyclonal anti-insulin primary antibody (1:100; sc-9168; Santa Cruz Biotechnology, Inc., Dallas, TX, USA) in phosphate-buffered saline (PBS) overnight at 4°C. After three extensive washes with PBS, the sections were incubated with a goat anti-rabbit IgG biotin-conjugated secondary antibody (1:2,000; sc-2040; Santa Cruz Biotechnology, Inc.) for 20 min at 32°C. After further incubation with horseradish peroxidase-labeled streptavidin, antibody binding was visualized using diaminobenzidine, and the sections were counterstained with hematoxylin. Tissue slides were visualized using a Wolfe S9-0982 microscope (Carolina Biological Supply Co., Burlington, NC, USA). Images were captured using a Canon powershot SX500 IS digital camera (Canon, Inc., Tokyo, Japan).
Statistical analysis
Results are expressed as the mean ± standard error for five independent rats per group. The statistical significance of the differences between groups was assessed using analysis of variance and post hoc descriptive analysis with SPSS software for Windows, version 11.5 (SPSS, Inc., Chicago, IL, USA). P<0.05 was considered to indicate a statistically significant difference.
Results
Changes in the serum levels of insulin, glucose and various lipid parameters
As shown in Table II, the induction of T2DM and IR increased the serum levels of glucose, TC, TG, LDL and VLDL, while decreasing the levels of HDL and insulin. By contrast, metformin administration for 4 weeks mitigated these elevations in all the parameters measured and increased the HDL levels and insulin secretion, supporting the beneficial effects of metformin in the treatment of IR and T2DM.
 | Table II.Serum changes in insulin, glucose and lipid profiles during insulin resistance and following metformin administration. |
Metformin normalizes the T2DM-induced alterations in the expression levels of genes associated with lipid metabolism
Semi-quantitative RT-PCR analysis was performed for hepatic acyl-CoA oxidase (ACO), carnitine palmitoyl transferase-1 (CPT-1), apolipoprotein C-III (apo C-III) and fetuin-A in the normal control, T2DM and T2DM + metformin rats. During T2DM and IR, a disturbance in lipid profiles typically occurs and alterations in the expression of genes associated with lipid metabolism may be observed (6). Therefore, alterations in the expression levels of ACO, CPT-1, apo C-III and fetuin-A were analyzed in the rat livers. Fatty acid oxidation was reduced during IR, as indicated by the expression levels of ACO and CPT-1 (Fig. 1A and B). However, metformin administration for 4 weeks increased the expression levels of ACO and CPT-1 (Fig. 1A and B), which appeared to improve the dyslipidemia observed in the T2DM rats. In contrast to ACO and CPT-1, the expression levels of apo C-III and fetuin-A increased in the T2DM rats, and metformin administration decreased their expression to approximately normal levels (Fig. 1C and D).
Metformin normalizes the T2DM-induced alterations in the expression levels of insulin signaling molecules
Semi-quantitative RT-PCR analysis was performed for hepatic insulin receptor substrate (IRS)-1 and IRS-2, fatty acid synthetase (FAS) and peroxisome proliferator activated receptor (PPAR)-α in the normal control, T2DM and T2DM + metformin rats. As shown in Fig. 2A and B, insulin signaling was reduced as a result of IR and T2DM, as indicated by the reduction in the expression levels of IRS-1 and IRS-2. By contrast, the expression of FAS was increased during IR due to the increase in fatty acids synthesis and lipogenesis, while metformin administration normalized the FAS expression levels (Fig. 2C). PPAR-α expression was increased following the administration of metformin (Fig. 2D), which indicated that the effects of metformin were gene specific.
Metformin normalizes the expression levels of perilipin and retinol binding protein-4 (RBP-4) in adipose tissue
Semi-quantitative RT-PCR analysis was performed for perilipin and RBP-4 in the adipose tissue of the normal control, T2DM and T2DM + metformin rats. As shown in Fig. 3, perilipin expression levels decreased significantly following the induction of T2DM and IR, while RBP-4 expression levels increased. Administration of metformin to the T2DM rats normalized the perilipin expression levels, as compared with the normal control and T2DM rats, and reduced RBP-4 expression after 4 weeks of administration.
Hepatic histopathological and pancreatic immunohistochemical changes in normal, T2DM and T2DM + metformin rats
Liver tissue from the healthy control rats exhibited a normal hepatic architecture, represented by normal hepatic lobules with a thin walled central vein and hepatic cords radiating towards the periphery, alternating with hepatic sinusoids (Fig. 4A). The liver tissue of the T2DM/IR rats presented with signet-ring hepatocyte morphology due to the extensive accumulation of fat replacing the hepatic cytoplasm or appearing as numerous small fat droplets (Fig. 4B). However, the liver tissue collected from the T2DM + metformin rats exhibited restoration of the normal hepatic architecture, with a reduction in the degree of fat droplet accumulation from the hepatocyte cytoplasm and regeneration of the hepatic parenchyma (Fig. 1C). The pancreas of the healthy control rats presented a normal architecture with normal insulin expression in the pancreatic β cells (Fig. 4D). However, the pancreatic tissue samples from the T2DM rats exhibited a reduction in the expression of insulin, with mild atrophy of the pancreatic β cells (Fig. 4E). Finally, the pancreas of the T2DM + metformin rats exhibited regenerative restoration of normal expression of insulin in the pancreatic β cells (Fig. 4F).
Discussion
In the present study, metformin was observed to ameliorate a number of the alterations in the serum and gene expression levels that occurred as a result of T2DM/IR. Metformin ameliorated the alterations associated with IR, including lipid profiles, insulin expression and glucose levels. Furthermore, the T2DM-induced alterations in the expression levels of genes associated with lipid metabolism were normalized following metformin administration. The metabolic action of insulin in liver tissue occurs in response to the activation of the phosphatidyl inositol 3 kinase (PI3K) pathway, in which the insulin receptor is activated by autophosphorylation after binding to insulin (21). The activated insulin receptor subsequently phosphorylates selective tyrosine residues on IRS and induces the binding of IRS-1 and IRS-2 to PI3K, phosphorylating serine and activating protein kinase B (PKB). The activation of PKB is crucial for various processes, including glucose transport in the liver, muscle and adipose tissue, glycogen synthesis in the liver and muscle tissue and lipogenesis in the adipose tissue (22). The phosphorylation of IRS-1 by serine kinases disrupts the interaction between the insulin receptor and IRS, thus preventing the tyrosine phosphorylation of IRS (21). These previously observed mechanisms are consistent with the results of the present study, since IR was observed to downregulate insulin receptor signaling, while metformin upregulated insulin receptor signaling and mitigated the dyslipidemia associated with IR. In accordance, Elmadhun et al (22) demonstrated that metformin supplementation in a T2DM rat model significantly altered the insulin signaling pathway. The insulin signaling cascade is initiated by insulin binding to the insulin receptor, resulting in tyrosine phosphorylation of IRS, which activates IRS and allows binding to PI3K. Subsequently, PI3K activates PKB, which initiates the translocation of intracellular glucose transporter-4 (GLUT-4) vesicles to the plasma membrane (23).
The administration of metformin has been previously demonstrated to improve hepatic insulin sensitivity by modulating the insulin signaling pathway in high fat-fructose diet (HFFD)-fed IR rats (24). Consumption of a HFFD resulted in hyperglycemia, hyperinsulinemia, increased gluconeogenesis and the reduced tyrosine phosphorylation of insulin receptor-β and IRS-1 (24). The authors observed that the administration of metformin reversed all the parameters altered by consumption of the HFFD. The present study demonstrated that the improved insulin sensitivity induced as a result of metformin treatment is mediated by enhanced tyrosine phosphorylation of IRS-1 and IRS-2. Grisouard et al (25) and unpublished data from the current research group indicated that metformin increases the mRNA expression levels of GLUT-4, and subsequently increases GLUT-4 protein levels in storage vesicles and the plasma membrane. Notably, GLUT-4 levels are lower in the adipocytes of obese patients and individuals with diminished glucose tolerance or T2DM (26).
Numerous approaches have been investigated with the aim to mitigate the damaging effects of IR by reducing the accumulation of detrimental lipids in muscle and liver tissue. Certain approaches have attempted to decrease the availability of TG and non-esterified fatty acids in circulation, in which the administration of PPAR-α agonists has been demonstrated to be successful (27). PPAR-α is a transcription factor that exerts notable effects on lipid homeostasis by regulating the expression of genes involved in lipid metabolism (27). The transcription factor is primarily expressed in the liver, where it regulates the transcription of genes involved in lipid uptake and oxidation, such as acyl-CoA synthetase (ACS), ACO, CPT-1 and lipoprotein lipase (LPL) (28). The activation of these factors is hypothesized to result in the sequestration of lipid into the liver for oxidation, which is demonstrated by the results of the present study (Fig. 2D). This activity putatively reduces the quantity of lipid available to the skeletal muscle, which is the most prevalent insulin-sensitive tissue type in humans (28). Following activation, PPAR-α is able to heterodimerize with the retinoid X receptor and bind with peroxisome proliferator response elements, which are located in the promoter regions of various genes, such as LPL (29), ACO (30), ACS (31) and CPT-1 (32), the transcription of which is activated by the complex. However, the expression of apo C-III is suppressed by PPAR-α activation due to the competition for a response element between the PPAR-α-retinoid X receptor heterodimer and hepatocyte nuclear factor-4, a liver enriched transcriptional activator (33).
The results of the present study indicate that metformin administration reduces the hepatic mRNA expression of apo C-III. Apo C-III inhibits the hydrolysing function of LPL, which is consistent with the observed reduction in the hepatic expression levels of apo C-III in the T2DM + metformin rats. The metformin-induced elevation in the mRNA expression levels of CPT-1 in the hepatic tissue may account for the increased level of β-oxidation in the liver tissue. Although metformin was not shown to directly enhance the expression of PPAR-α, the drug was observed to increase the mRNA expression levels of hepatic ACO, which is a well-known marker of PPAR-α activation. In addition, similar to typical PPAR-α activators, metformin reduced the mass of visceral fat. These results indicate that metformin may function as a PPAR-α agonist.
In a previous study, significant reductions were observed in the plasma levels of TG, TC and insulin, body weight, abdominal fat weight, hepatic lipid content and hepatic FAS expression in laying hens with non-alcoholic fatty livers administered metformin at 100 mg/kg body weight; however, a significant increase was observed in the expression levels of CPT-1 (34). Collectively, these previous findings and the results of the present study confirm the efficacy of metformin for the treatment of IR. In addition to the induction of lipolytic enzymes, metformin may also function as an activator of adenosine monophosphate-activated protein kinase (AMPK) (35). The activation of AMPK phosphorylates acyl-CoA cyclase (ACC) and subsequently inhibits its activity, which leads to a reduction in malonyl-CoA synthesis. This reduction may in turn stimulate the transportation of fatty acids into the mitochondria for β-oxidation via the upregulation of CPT-1, a transporter of fatty acids (36). Furthermore, metformin increases the phosphorylation of mitogen-activated protein kinase (MAPK) and ACC, and the expression of CPT-1, which suggests that metformin enhances fatty acid β-oxidation.
In addition to enhancing the rate of lipolysis and fatty acid oxidation in mitochondria, metformin reduces the expression of FAS, a lipogenic protein. FAS catalyzes the final step in the fatty acid biosynthetic pathway and is crucial for determining the maximum capacity of a tissue for synthesizing fatty acids via the de novo pathway (37). The results of the present study indicate that metformin may exert this lipid-reducing activity via the concerted modulation of lipolysis and lipogenesis, in which the expression levels of hepatic genes associated with lipid metabolism are altered. These findings are consistent with those of a previous clinical study, which indicated that a combination of insulin and metformin reduced hepatic steatosis and TG levels in patients with T2DM (38). In addition, Bhalla et al (39) observed that metformin reduced the mRNA and protein expression levels of a number of lipogenic enzymes, such as FAS, which is consistent with the results of the present study.
Fetuin-A is a 60 kDa glycoprotein that is secreted by hepatocytes, and can be used as a biomarker of liver function and inflammation. Fetuin-A modulates insulin signal transduction by inhibiting the insulin receptor tyrosine kinase in the liver and skeletal tissue, as well as inhibiting the autophosphorylation of the insulin receptor in vitro and in vivo, which ultimately results in IR (10). Furthermore, increased fetuin-A levels have been associated with obesity, IR, metabolic syndrome, liver fat accumulation and an increased risk of T2DM (10). In the present study, fetuin-A expression was shown to increase in the T2DM rats, while treatment with metformin was able to restore fetuin-A expression. Fetuin-A has been demonstrated to suppress the generation of adiponectin in adipose tissue, and fetuin-A treatment in wild-type mice may result in hypoadiponectinemia (10). In addition, reduced levels of adiponectin may induce the accumulation of fat in the liver, resulting in increased fetuin-A secretion (40). Therefore, elevated fetuin-A expression may lead to reduced levels of adiponectin in obese patients with T2DM, as indicated in a study by Mori et al (10).
An additional lipid metabolism regulating gene is perilipin, which has the function of coating the surface of intracellular lipid droplets in adipocytes. Perilipin modulates lipolysis (41) through limiting the interaction between lipase and the TG core stored within the lipid droplets (42). The results of the present study demonstrated that metformin normalized the IR-induced reduction in the expression of perilipin in the adipose tissue of T2DM rats. In addition, the treatment of adipocytes with metformin has been shown to attenuate lipolytic activity, stimulated by tumor necrosis factor (TNF)-α, isoproterenol or a high dose of glucose (43). The inhibitory effect of metformin on TNF-α-stimulated lipolysis is accompanied by the suppressed phosphorylation of extracellular signal-regulated kinases 1/2 and the reversed downregulation of perilipin. These two effects may primarily account for the molecular basis underlying the antilipolytic function of metformin in TNF-α-stimulated adipocytes.
A previous study revealed that RBP-4 is the only specific transport protein for retinol (vitamin A) that is able to deliver retinol to tissues from the blood (44). RBP-4 is highly expressed in adipose tissue, as compared with liver tissue, and is strongly associated with endothelial function (44). Fischer et al (45) reported that a reduction in RBP-4 secretion results in improved insulin levels (44). Previously, RBP-4 serum levels appeared to be associated with insulin sensitivity, and were increased in obese non-diabetic subjects (44) and patients with T2DM (46). Limited data is available with regard to the exact role of RBP-4 in human metabolism. However, a previous study reported a marked correlation between RBP-4 and IR in non-diabetic subjects without a medical or family history of diabetes (47).
Furthermore, a prior study demonstrated that high secretion of RBP-4 by adipocytes reduced the expression of GLUT-4 in adipose tissue, which is commonly observed in patients with T2DM (47). The results of the present study are consistent with those of Tajtáková et al (48), since obese patients with T2DM treated with metformin were shown to exhibit lower plasma RBP-4 levels compared with obese patients, indicating that metformin may improve total insulin sensitivity through RBP-4. Recently, the insulin sensitizer, rosiglitazone, has been reported to significantly decrease the RBP-4 levels, and thus, mitigate IR (49). Therefore, RBP-4 may be useful as a clinical marker for identifying individuals at risk of developing IR or T2DM. In addition, it is possible that metformin exerts its effects via the regulation of RBP-4.
T2DM is characterized by progressive β cell destruction, as a result of chronic IR and the loss of β cell mass and function, as shown in Fig. 4E and demonstrated by previous studies (50,51). The primary mechanism underlying the reduction in β cell mass in patients with T2DM is the apoptosis of β cells in all diabetic patients. However, β cell mass is affected by numerous factors, including cell size, rate of cell renewal or neogenesis and the rate of apoptosis (51). In patients with T2DM, pancreatic β cells are unable to secrete sufficient quantities of insulin to compensate for the reduced insulin sensitivity, which is primarily a result of insulin secretion dysfunction and a marked reduction in the number of functional β cells (Fig. 4E) (50–54). Consistent with these findings, the present study observed similar effects, as metformin administration participated in the regeneration of the capacity of pancreatic β cells to secrete insulin. In the T2DM + metformin group rats, restoration of normal β cell mass was observed. Thus, the antidiabetic effects of metformin may occur as a result of the reduction of hepatic gluconeogenesis, the regeneration of hepatocytes (Fig. 4C), reduced glucose absorption and increased insulin sensitivity (Fig. 4F), through the increase in glucose uptake and utilization (55,56).
In conclusion, the results of the present study demonstrated the beneficial effects of metformin in the treatment of IR. Metformin was observed to normalize IR-associated dyslipidemia. Furthermore, metformin was demonstrated to regulate the expression of various genes associated with lipid metabolism. Notably, close associations were observed between metformin and a number of genes expressed in the liver and adipose tissue, including fetuin-A, perilipin and RBP-4. However, further studies are required to outline the molecular signaling pathways affected by metformin in the amelioration of IR.
Acknowledgements
The study was supported by a grant from The Deans of Scientific Affairs, Taif University (no. 2220-1-1434; Ta'if, Saudi Arabia).
Abbreviations:
|
ACO |
acyl-CoA oxidase |
|
ACS |
acyl-CoA synthetase |
|
AMPK |
adenosine monophosphate-activated protein kinase |
|
MAPK |
mitogen-activated protein kinase |
|
apo C-III |
apolipoprotein C-III |
|
CNS |
central nervous system |
|
CPT-1 |
carnitine palmitoyl transferase-1 |
|
FAS |
fatty acid synthetase |
|
GLUT-4 |
glucose transporter-4 |
|
HDL |
high-density lipoprotein |
|
HFD |
high-fat diet |
|
HFFD |
high-fat fructose diet |
|
IR |
insulin resistance |
|
IRS |
insulin receptor substrates |
|
LDL |
low-density lipoprotein |
|
LPL |
lipoprotein lipase |
|
PI3K |
phosphatidyl inositol 3 kinase |
|
PKB |
protein kinase B |
|
PPAR-α |
peroxisome proliferator activated receptor-α |
|
PBS |
phosphate-buffered saline |
|
RT-PCR |
reverse transcription-polymerase chain reaction |
|
RBP-4 |
retinol binding protein-4 |
|
STZ |
streptozotocin |
|
T2DM |
type 2 diabetes mellitus |
|
TC |
total cholesterol |
|
TG |
triglycerides |
|
VLDL |
very low-density lipoprotein |
|
ACC |
acyl-CoA cyclase |
|
TNF |
tumor necrosis factor |
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