Expression of melanocortin-4 receptor and agouti-related peptide mRNAs in arcuate nucleus during long term malnutrition of female ovariectomized rats
Objective: Melanocortin-4 receptor (MC4R) and agouti-related peptide (AgRP) are involved in energy homeostasis in the rat. The aim of the present study was to evaluate the expression of MC4R and AgRP mRNAs in arcuate nucleus (ARC) during long term malnutrition of female ovariectomized rats.
Materials and Methods: Twelve female ovariectomized rats were divided into two equal groups (n=6) of normal and restricted diet groups. Four ovariectomized rats were selected as controls. Using real-time PCR, the relative expressions (compared to controls) of MC4R and AgRP mRNAs in the ARC of rats were compared between both diet groups.
Results: The relative expression of MC4R and AgRP mRNA in the ARC of female ovariectomized rats during long term malnutrition was higher than those with normal diet (P<0.05).
Conclusion: Changes in the relative expression level of MC4R and AgRP mRNAs during long term malnutrition of rat indicated a stimulatory role of MC4R and AgRP in regulating energy balance in ARC of rat hypothalamus.
Keywords: Melanocortin-4 receptor, Agouti-related peptide, Hypothalamus, Malnutrition, Rat
Melanocortin-4 receptor (MC4R) is the cognate receptor for α-melanocyte stimulating hormone (α-MSH), a cleavage product of proopiomelanocortin (POMC) which is expressed in hypothalamic arcuate nuclei (ARC) neurons (1). This receptor belongs to the melanocotrin receptors and one of the members of G protein-coupled receptors that activates adenylate cyclase (2). MC4R neurons have been observed in ARC, periventricular nuclei (PVN) and medial preoptic area (MPO) and preoptic area (POA) of hypothalamus of rats which these nuclei are involved in regulate appetite (3-5). MC4R blockage relieved an anorectic condition in rat (6). Moreover, MC4R agonist suppresses food intake when administered to rats and mice that lack functional leptin receptors (7). Conversely, centrally administration of a selective MC4R antagonist potently increased food intake in rats (7). Activation of MC4R by agonists such as α-MSH inhibits feeding and causes weight loss (3). In rodents, stimulation of MC4R causes a reduction in food intake, whereas antagonism of MC4R increases food intake (8). MC4R regulates both sides of the energy intake/energy expenditure balance (9).
Agouti related peptide (AgRP), a MC4R antagonist, stimulated feeding and caused obesity (3). AgRP is the neuropeptide with 132 amino acid that are expressed in the ARC of mice (10) and sheep (11). Using immunohistochemistry, AgRP-containing cell bodies were found almost exclusively in the ARC, but their projections were distributed widely in the hypothalamus, most conspicuously in the PVN, ARC, dorsomedial nuclei, and the posterior hypothalamic area (12). In some species, AgRP neurons are involved in energy balance (13). AgRP is an appetite stimulus (14) and increases during the lack of energy (15). Perfusion of monkey and rodents with AgRP increase food intake (16). Intracerebroventricular (ICV) injection of AgRP, increased food intake and inhibited α-MSH in the rat (16). Mice with deficient in the MC4R expression (17) or high expression of AgRP (18) were fat. Various hormones such as insulin, leptin and glucocorticoids could change AgRP expression based on homeostasis mechanism (14). Neuropeptide Y (NPY) and the endogenous MC4R antagonist, AgRP, coexist in the ARC, and both exert orexigenic effects (19). Ectopic AgRP expression in the hypothalamus causes obesity in the mouse, while AgRP is expressed by NPY neurons in the ARC (3) and NPY is expressed by neurons that project to important appetite-regulating nuclei, including the PVN (3). NPY injected into the PVN is the most potent central appetite stimulant known (3). The NPY neurons in the ARC are stimulated by starvation, probably mediated by decreases in circulating leptin and insulin (which both inhibit these neurons), and contribute to the increased hunger in energy deficit conditions (3).
These results support the hypothesis that the brain MC4R and AgRP is intimately involved in the control of food intake and act homeostatically to correct negative energy balance. Therefore the aim of the present study was to investigate MC4R and AgRP mRNAs expression in the ARC during long term malnutrition of female ovariectomized rats.
Material and methods
Sixteen female adult (3-4 months old) Sprague-Dawley rats (Rattus norvegicus) that weighed 200±20 g (mean ± SD) were randomly selected from the Laboratory Animal Center of Shiraz University of Medical Sciences, Shiraz, Iran. They were housed under controlled temperature (22±2°C), humidity (60±6%) and light (12 h light to 12 h dark ratio; lights on at 7:30 AM) conditions. All experimental procedures were carried out between 12.00-2.00 pm and in compliance with the Animal Care Committee recommendations of the Shiraz University of Medical Sciences. Standard rat feed (before the start of the study) and water were freely available to them. The rats were ovariectomized to remove the effects of reproductive hormones during the estrous cycle. The rats were anesthetized by ketamine (intraperitoneal injection, 100 mg/kg, Woerden, Netherlands) and xylazine (intraperitoneal injection, 7 mg/kg, Alfazyne, Woerden, Netherlands). They were ovariectomized through a ventral midline incision and after a two week recovery period, further procedures were undertaken.
Standard rat diet contained 90% dry matter, 8% ash, 4.1% crude fat, 21.6% crude protein, 70.8% total digestible nutrients (TDN), 0.4% calcium, 0.35% potassium and 0.1% sodium, which were measured based on AOAC, 1995. Two weeks after surgery, 12 rats were randomly divided into two equal groups and the first group were fed with a complete ration (15 g/kg) of standard rat diet (normal diet group, n=6) and the other group with a half ration (7.5 g/kg) of the first group (restricted diet group, n=6) for 14 days and then were anesthetized with ether and were ethically killed. Four rats of control group were ethically killed two weeks after surgery (day 0).
The rats were decapitated, brains immediately dissected out, and the diencephalon was dissected out by an anterior coronal section, anterior to the optic chiasm, and a posterior coronal cut at the posterior border of the mammillary bodies. To separate ARC from other nuclei, a third coronal cut was made through the middle of the optic tract, just rostral to infundibulum (20). The specimens consisted of ARC and DMH were stored in liquid nitrogen and then stored at -80°C. RNA extraction, DNase treatment, cDNA synthesis and relative real-time PCR procedure were performed as described elsewhere (21). Primers were designed with Allele ID 7 software for the reference gene, AgRP (NM_033650.1) and MC4R (NM_013099.2). The rat glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene (M32599) was used as reference gene for data normalization (Table 1).
Relative expressions of AgRP and MC4R based on the threshold cycle (CT) method were calculated for quantitative real-time PCR data. Using Line-gene K software (22), CT for each sample was calculated. Fold expression of the target mRNAs over reference values was calculated by the equation 2-ΔΔCT (23), where ΔCT is determined by subtracting the internal control (corresponding GAPDH CT value) from the specific CT of the AgRP or MC4R. ΔΔCT was obtained by subtracting the ΔCT of each experimental sample from that of the control ovariectomized rats.
Normality of the data on the relative expression of AgRP and MC4R mRNAs were evaluated by Kolmogorov-Smirnov test using SPSS version 11.5 (SPSS Inc, Chicago, Illinois). Expression of AgRP and MC4R mRNAs were compared between groups using independent sample t-test. Correlation coefficient of their expression was analyzed by Pearson correlation test. We considered P<0.05 as significant.
Expression of AgRP (P=0.048, Fig 1) and MC4R (P=0.027, Fig 2) mRNAs in the ARC of restricted diet group of female ovariectomized rats was more than normal diet group. Food-restricted rats showed a 6.2 fold increase in the expression of AgRP mRNA in the ARC of the hypothalamus. Moreover, the expression of MC4R mRNA increased 6.7 times in long term food-restricted in comparison with normal feeding female rats. A positive correlation was observed between expression of AgRP and MC4R mRNAs in the ARC of female ovariectomized rats of both diet groups (r=0.99, P<0.001, Fig 3).
Conflict of interest
There is no financial interest.
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Table 1: Sequences of real-time PCR primers used to evaluate relative expression of AgRP and MC4R genes in the rat
Amplicon length (bp)
5` TGGGTGTCATAAGCCTGTTGG 3`
5` GCGTCCGTGTCCGTACTG 3`
5` TGAAGAAGACAGCAGCAGACC 3`
5` TGAAGAAGCGGCAGTAGCAC 3`
5` AAGAAGGTGGTGAAGCAGGCATC 3`
5` CGAAGGTGGAAGAGTGGGAGTTG 3`
Fig 1. Mean (± standard error) of the relative expression of agouti-related peptide (AgRP) mRNAs in the arcuate nucleus (n=6) during long term malnutrition in female ovariectomized rats. Different letters indicate significant difference (P<0.05).
Fig 2. Mean (± standard error) of the relative expression of melanocortin-4 receptor (MC4R) mRNAs in the arcuate nucleus (n=6) during long term malnutrition in female ovariectomized rats. Different letters indicate significant difference (P<0.05).
Fig 3. Correlation of the relative expression of agouti-related peptide (AgRP) and melanocortin-4 receptor (MC4R) mRNAs in the arcuate nucleus (n=6) in female ovariectomized rats.