IGF-I Gene Expression Research Articles

Exogenous phytase and xylanase supplementation of formulated diets for rohu (Labeo rohita): impact on haematology, histology and IGF I gene expression.

The present study aims to delineate the effect of exogenous enzyme supplementation of fermented or non-fermented de-oiled rice bran (DORB) on haematology, histology and expression of IGF I gene expression of Labeo rohita. Four test diets, namely, T1 (DORB), T2 (fermented DORB), T3 (DORB+exogenous enzyme) and T4 (fermented DORB+exogenous enzyme) were formulated and fed to the L. rohita for a period of 60 days. The test diets T3 and T4 were supplemented with 0.1 g kg-1 xylanase (16,000 U kg-1) and 0.1 g kg-1 phytase (500 U kg-1) enzymes. A total of 120 juveniles of L. rohita (average weight 5.01 ± 0.02 g) were stocked in 12 rectangular tanks with 10 fish per tank in triplicates. At the end of the experiment, haematology, histology and IGF I gene expression of the different groups were analysed. The haemoglobin (Hb) content, RBC count and WBC count of L. rohita varied significantly (p < 0.05) among different groups. T3 diet-fed group had the highest Hb content, RBC count and WBC count as compared to the other groups. The MCV content was significantly (p < 0.05) lower in T3 group. The DORB type, exogenous enzyme supplementation and their interaction have no significant (p > 0.05) effect on MCH, MCHC and lymphocyte content of the cultured fish. The group which were fed T3 diet had significantly (p < 0.05) higher IGF-I gene expression as compared to other groups. The histological examination of liver revealed no pathological alteration of this organ. Similarly, there were no pathological changes observed in intestinal tissue in any dietary treatment group. Based on the findings of the present study, it is concluded that exogenous enzyme supplementation of DORB-based diets improves the physiological status and growth performances of Labeo rohita.

Analysis of the Gene Expression Profile of Stromal Pro-Tumor Factors in Cancer-Associated Fibroblasts from Luminal Breast Carcinomas.

Luminal tumors are the most frequent type of breast carcinomas showing less tumor aggressiveness, although heterogeneity exists in their clinical outcomes. Cancer-associated fibroblasts (CAFs) are a key component of the tumor stroma which contribute to tumor progression. We investigated by real-time PCR the gene expression of 19 factors implicated in tumor progression. Those factors included the calcium-binding protein S100A4, several growth factors (FGF2, FGF7, HGF, PDGFA, PDGFB, TGFβ, VEGFA, and IGF2), and we also studied inflammatory cytokines (IL6 and IL8), chemokines (CCL2, CXCL12), important proteases (uPA, MMP2, MMP9 and MMP11), the nuclear factor NFκB, and the metalloprotease inhibitor TIMP1, from luminal A and luminal B breast carcinoma CAFs. We performed a similar analysis after co-culturing CAFs with MCF-7 and MDA-MB-231 breast cancer cell lines. MMP-9 and CCL2 gene expressions were higher in CAFs from luminal B tumors. We also found different patterns in the induction of pro-tumoral factors from different CAFs populations co-cultured with different cancer cell lines. Globally, CAFs from luminal B tumors showed a higher expression of pro-tumor factors compared to CAFs from luminal A tumors when co-cultured with breast cancer cell lines. Moreover, we found that CAFs from metastatic tumors had higher IGF-2 gene expression, and we detected the same after co-culture with cell lines. Our results show the variability in the capacities of CAFs from luminal breast carcinomas, which may contribute to a better biological and clinical characterization of these cancer subtypes.

Influence of Lacto-Immuno-Vital on growth performance and gene expression of IgA, MUC-2, and growth factor IGF-2 in the jejunum of broiler chickens

The effects of Lacto-Immuno-Vital synbiotic preparation on gene expression of IgA, MUC-2, and growth factor IGF-2 in the jejunum and on BW gain in broiler chickens were studied. A flock of 64,400 1-day-old Hybrid ROSS 308 chickens was inducted in the 42-day experiment. The chickens were divided into 2 equally size groups in separate halls. The chickens in the experimental (E) group received 500 g of Lacto-Immuno-Vital in 1,000 L of drinking water. The preparation was administered daily from the first day (day 1) to day 7 of the experiment. From day 7 to day 22, it was given in pulsed manner (every third day) at a dose of 300 g in 1,000 L of drinking water. The broiler chickens in the E group gained more weight (P < 0.001) compared with control from day 10 to day 42. Death of animals during feeding period was 1,078 chickens in the E group compared with 1,115 dead chickens in the control group. Feed conversion ratio was 1.61 kg of supplemented diet/kg of BW in the E group compare with 1.67 kg of nonsupplemented diet/kg of BW in control. The relative expression of IgA gene in the jejunum was upregulated on day 22 in the E group compared with control (P < 0.05), whereas relative expression of MUC-2 gene was upregulated in the E group compared with control on day 8 and day 22 (P < 0.05; P < 0.001). Similarly, relative expression of IGF-2 gene was upregulated in the E group compared with control on both samplings (P < 0.01). The composition of Lacto-Immuno-Vital synbiotic preparation showed beneficial effects on growth performance, feed conversion ratio, morbidity, mortality, and selected parameters of mucosal immunity in the chicken jejunum.

Genetic and Hormonal Difference between High Growth Rate Breed (Cobb Broiler chicken) and Low Growth Rate Breed (Native Fayoumi chicken)

Abstract The present study aimed at investigating the genetic and hormonal differences between a low growth rate chicken breed (a native breed: Fayoumi chicken) and a high growth rate chicken breed (Cobb broiler chicken). A total number of 100 one-day-old Fayoumi chicks and 100 one-day-old Cobb chicks were used. Chicks of each breed were allocated into three equal replicates. The growth parameters (body weight, BWG and FCR), genetic expression of some growth related genes (GH, IGF1, ghrelin and Myostatin gene) and plasma level of some growth related hormones (Insulin, T3, T4 and corticosterone) were recorded. The obtained results revealed that, Cobb chicken had significantly higher body weight, BWG and feed intake than Fayoumi chicken but the FCR of Fayoumi chicken was higher than that of broiler chicken. Cobb recorded significantly lower plasma level of corticosterone, T3 and T4 than Fayoumi chicken while Insulin is higher in cobb chicken. Cobb recorded highly significant values of GH, IGF1 and ghrelin Gene expression while myostatin gene expression was higher in Fayoumi chicken than in Cobb From the obtained results could be concluded that, the observed high growth rate in cobb chicken may be attributed the difference gene expression related growth as well as hormonal difference

Downregulation of IGF2 expression in third trimester placental tissues from Zika virus infected women in Brazil

ObjectivesScreening for genes differentially expressed in placental tissues, aiming to identify transcriptional signatures that may be involved in ZIKV congenital pathogenesis. MethodsTranscriptome data from placental tissues of pregnant women naturally infected with Zika virus during the third trimester were compared to those from women who tested negative for Zika infection. The findings were validated using both a cell culture model and an immunohistochemistry/morphological analysis of naturally infected placental tissues. ResultsTranscriptome analysis revealed that Zika virus infection induces downregulation of insulin-like growth factor II (IGF2) gene, an essential factor for fetal development. The Caco-2 cell culture model that constitutively expresses IGF2 was used for the transcriptome validation. Asiatic and African Zika virus strains infection caused downregulated IGF2 gene expression in Caco-2 cells, whereas other flaviviruses, such as dengue serotype 1, West Nile and wild-type yellow fever viruses, had no effect on this gene expression. Immunohistochemical assays on decidual tissues corroborated our transcriptome analysis, showing that IGF2 is reduced in the decidua of Zika virus-infected women. ConclusionsOur results draw attention to IGF2 modulation in uterine tissues, and this finding is expected to support future studies on strategies to ameliorate the harmful effects of Zika virus infection during pregnancy.

Expression of the insulin-like growth factor (IGF) gene family in feline uterus during pregnancy

ABSTRACT Members of the IGF gene family participate in cell differentiation and proliferation during pregnancy. We used 35 cats assigned to experimental groups (G) based on pregnancy stages: G1, pre-implantation; G2, implantation; G3, early pregnancy; G4, mid-pregnancy; G5, nonpregnant. Quantitative polymerase chain reaction (qPCR) and immunohistochemistry were used to analyze the expression of the IGF gene family. During pregnancy, expression of IGF-1 gene was significantly greater at implantation sites in the G1 and G2 groups than at placentation sites in G3 and G4 groups. IGF-2 expression was greater in the G2, G3 and G4 groups than in G1. Expression of the IGF-1R gene was significantly greater at placental sites in G3 than in G1 and G4. IGF-2R genes were expressed in all groups. Insulin-like growth factor binding proteins (IGFBPs) were expressed at intensities that depended on the stage of pregnancy; they were detected in different cell types and at different sites in the uterus. We found that members of the IGF gene family were expressed differentially in the endometrium during pregnancy. Our findings suggest that the IGF family may be a regulatory factor for pregnancy in cats.

IGF-I gene expression in liver and white muscles confirming promotion effect of dietary NaCl on Growth indices of Giant sturgeon (Huso huso) juveniles

TThis study was conducted to evaluate effects of different levels of NaCl used in the diet of cultivated Huso huso juveniles based on gene expression of Insulin-like Growth Factor (IGF), IGF mRNA in the liver and muscle. Totally 480 specimen beluga juvenile by the average weight of 173.8±0.49 g stocked in 12 tanks and reared for 12 weeks. The NaCl added in 4 levels and with three replicates of 0(control), 3, 6 and 9 percent to the basic diet. After 12 weeks total RNA extracted from the16 liver and muscle which were sampled from two replicates of treatments and evaluated by electrophoresis. β2m-qPCR primer was used as gene reference. The size of the product obtained from primers and the specific degree of action of primers was confirmed using agarose gel (1.5%) and the sequencing of the genes.According to the results, significant changes in IGF mRNA expression observed in the treatments and control group (p <0.05). The data of IGF gene expressions showed that the highest levels observed in the control group and treatment 3% respectively. Moreover, in the tissue of white muscle, IGF mRNA gene expression showed highest gene expression in the control group (6.4) and lowest expression were in treatment 3% (0.7) and treatment 6% (0.8). Also, growth indices results including body weight, Specific Growth Rate(SGR), Body Weight Index(BWI), Hepatosomatic Index(his) and Average Daily Growth(ADG) significantly were increased in all treatments, with significant differences among treatments and the control group (p <0.05). The SGR in the control group increased from 1.41 to 1.58 in treatments 3% and 6% and the BWI increased from 68.88 in the control group to 98.28 in treatment 6%. HSI increased from 3.64 g in the control group to 4.37 g in treatment two. FCR showed a significant difference in the control group (1.27) and 1.14 in 3% and 9%, respectively. Statistical analysis of FCR, SGR and IGF mRNA gene expression showed better growth indices in fish fed by a diet containing NaCl.

The effect of protease on growth performance, nutrient digestibility, and expression of growth-related genes and amino acid transporters in broilers.

During the course of this trial, our team assessed the influence of protease upon the growth performance, the nutrient digestibility, and the expression of growth-related genes and amino acid transporters within the liver, muscle, and small intestines of broilers. During the first step, our team allocated 600 broilers into four dietary treatments for a period of 35 days in order to measure the growth performance and nutrient digestibility of the broilers selected. The separate treatments contained 10 replicates (15 birds per replicate). The treatments were composed of: 1) CON, basal diet; 2) T1, basal diet + 0.03% protease; 3) T2, basal diet + 0.06% protease; and 4) T3, basal diet + 0.09% protease. Next, the broiler chick sample tissue was harvested from the CON and T3 groups in order to conduct gene expression analysis following the feeding trials the broilers underwent. Our team discovered that the broilers fed protease diets possessed increased body weight and an average daily gain, but conversely, had lower feed conversion ratios when their dietary protease levels increased from 0% to 0.09% (p < 0.05). Additionally, significant linear improvements were identified among the nutrient digestibility of dry matter, crude protein, energy, and amino acids within broilers supplied with protease diets when contrasted and compared with broilers supplied with the basal diet (p < 0.05). In addition, the gene expression of the genes IGF1, IGF2, GH, and LEP in the liver, and the genes MYOD1 and MYOG in the breast muscles, was significantly increased after broilers were fed with a protease diet as compared to broilers that subsisted on a basal diet (p < 0.05). Protease supplementation also raised the expression levels within these amino acid transporters: SCL6A19, SLC7A1, SLC7A7, SLC7A2, SLC7A6, SLC7A9, and SLC15A1, located in the small intestine, when compared to the basal diet (p < 0.05). Our results suggest that protease supplementation in their diet improved the growth performance of broilers via an increase in the expression growth-related genes within broiler liver and muscle tissue. In addition, protease supplementation enhanced broiler digestibility via the upregulation of amino acid transporter expression within the small intestine.

Effects of maternal low-protein diet and spontaneous physical activity on the transcription of neurotrophic factors in the placenta and the brains of mothers and offspring rats.

Maternal protein restriction and physical activity can affect the interaction mother-placenta-fetus. This study quantified the gene expression of brain-derived neurotrophic factor (BDNF), neurothrophin 4, tyrosine kinase receptor B (TrkB/NTRK2), insulin-like growth factor (IGF-1), and insulin-like growth factor receptor (IGF-1r) in the different areas of mother's brain (hypothalamus, hippocampus, and cortex), placenta, and fetus' brain of rats. Female Wistar rats (n = 20) were housed in cages containing a running wheel for 4 weeks before gestation. According to the distance spontaneously traveled daily, rats were classified as inactive or active. During gestation, on continued access to the running wheel, active and inactive groups were randomized to receive normoprotein diet (18% protein) or a low-protein (LP) diet (8% protein). At day 20 of gestation, gene expression of neurotrophic factors was analyzed by quantitative polymerase chain reaction in different brain areas and the placenta. Dams submitted to a LP diet during gestation showed upregulation of IGF-1r and BDNF messenger RNA in the hypothalamus, IGF-1r and NTRK2 in the hippocampus, and BDNF, NTRK2, IGF-1 and IGF-1r in the cortex. In the placenta, there was a downregulation of IGF-1. In the brain of pups from mothers on LP diet, IGF-1r and NTRK2 were downregulated. Voluntary physical activity attenuated the effects of LP diet on IGF-1r in the hypothalamus, IGF-1r and NTRK2 in the hippocampus, IGF-1 in the placenta, and NTRK2 in the fetus' brain. In conclusion, both maternal protein restriction and spontaneous physical activity influence the gene expression of BDNF, NTRK2, IGF-1, and IGF-1r, with spontaneous physical activity being able to normalize in part the defects caused by protein restriction during pregnancy.

How Different Stocking Densities Affect Growth and Stress Status of Acipenser baerii Early Stage Larvae.

Simple SummarySiberian sturgeon is a freshwater fish species currently at risk of extinction. Few studies have been performed on the environmental conditions during early larval stages, a phase of development where mortality rate is still relevant. In this study, we focused on assessing the impact of different rearing densities during the endogenous feeding stage of the Siberian sturgeon on growth, stress status, and muscle development, using a multidisciplinary approach. Results indicate that lower densities seem more advantageous in this stage of development in terms of growth rate and stress levels. However, rearing larvae at such low densities is not economically feasible in commercial hatcheries but it could be interesting, instead, in larvae production for repopulation purposes.In the present study, a multidisciplinary approach was used in order to evaluate growth, muscle development, and stress status in Siberian sturgeon Acipenser baerii larvae at schooling (T1) and complete yolk sac absorption (T2), reared at three stocking densities (low, medium, and high). Larvae growth, morphological muscle development, and whole-body cortisol levels were assessed. The expression of genes involved in the growth process (igf1 and igf2), in the myogenesis (myog), and in the regulation of cellular stress (glut1, glut2, glut4, and hsp70) was analyzed using a quantitative PCR. Larvae reared at lower densities showed a higher Specific Growth Rate and showed a physiological muscle development. Cortisol levels were low and did not differ significantly, both in different time sampling and across densities, suggesting that either the considered densities are not stressors in this species in the early stages of development or the hypothalamus-pituitary-adrenal (HPA) axis is not yet fully mature. Gene expression of glut1, igf1, and igf2 showed an up-regulation in both developmental stages at all the rearing densities considered, while myog significantly up-regulated at T1 at the highest density. Considering all of the results, it would seem that lower densities should be used in these stages of development, as these showed a higher growth rate, even if it is not economically feasible in commercial hatcheries. Therefore, choosing an intermediate stocking density could be a good compromise between larval performance and economical feasibility.

Evaluating antitumor activity of antiglypican-3 therapy in experimentally induced skin cancer in mice.

Glypican-3 (GPC3) is considered as a cell surface heparan sulfate proteoglycan. It is overexpressed in skin cancer and promotes tumor progression and pathogenicity. Therefore, we aimed to find out the therapeutic effects of immuno-suppressing GPC3 in skin cancer experimentally induced in mice as well as to underline molecular mechanisms especially inflammatory and apoptotic pathways. Skin cancer was experimentally induced in mice by repeated rubbing of mice skin with 7,12-dimethylbenz (a) anthracene. Mice were injected with anti-GPC3. Skin samples were isolated to investigate the gene and protein expression of GPC3, Wnt-1, NFκB, TNF-α, IGF-1, p38 MAPK and caspase-3 using PCR, Western blot and ELISA. Moreover, skin sections were stained with hematoxylin and eosin. Treating skin cancer mice with anti-GPC3 significantly blocked GPC3, which is accompanied by amelioration of skin cancer-induced increase in the numbers of tumors and scratching behavior. Moreover, anti-GPC3 attenuated skin cancer-induced increase in the expression of Wnt-1, NFκB, TNF-α, IGF-1, p38 MAPK and caspase-3. In parallel, anti-GPC3 reduced degeneration of melanocyte cells and reduced phagocytic cells epidermal hyperplasia and dysplasia in skin sections stained with hematoxylin and eosin stain. In conclusion, anti-GPC3 produced anti-tumor effects against skin cancer, which can be explained by reduction in both inflammatory and apoptotic pathways. Targeting GPC3 is a promising therapeutic approach for skin cancer.

Aerobic and resistance training improve alveolar bone quality and interferes with bone-remodeling during orthodontic tooth movement in mice.

The direct effects of physical activity on long bones are already recognized. However, little information is available regarding distant osseous sites, such as maxillary bone. We evaluated the influence of physical training on alveolar bone quality, with and without mechanically-induced load during orthodontic tooth movement in mice. Forty-two C57BL/6 mice were divided into sedentary, resistance and aerobic training groups. Training period lasted for eight weeks and mechanical loads (orthodontic tooth movement - OTM) were applied during the last 14days of training. Both types of training enhanced the quality of maxillary bone, increasing bone mineral density (BMD), trabecular bone volume (BV) and bone volume/total volume ratio (BV/TV). OTM significantly reduced in trained groups. Consistently, the number of osteoblasts increased whereas the number of osteoclasts decreased on the OTM side in trained groups in comparison to the sedentary group. IGF-1, RUNX2 and OPG genes expression were also increased. The RANKL/OPG ratio and IL-6 expression were reduced in the maxillary bone. Similar results were verified in the femoral bone. In line with these findings, physical training resulted in a decrease of osteoclast differentiation from femoral bone marrow; as well as the force required to fracture the tibia of trained animals increased. Physical training also caused EDL muscle hypertrophy and increased expression of IGF-1 and IGF-1/Myostatin ratio in the gastrocnemius muscle, whereas FNDC5 gene expression was similar among groups in femur, but decreased in alveolar bone submitted to OTM. In conclusion, physical training increased bone quality, not only on long bones, but also in a distant site such as the maxilla. Differences were more evident in the course of maxillary mechanical loading. Mechanisms involve systemic and local effects on bone cells and target molecules as RANKL, OPG, IL-6 and IGF-1.

A combination of rapeseed, cottonseed and peanut meal as a substitute of soybean meal in diets of Yellow River carp Cyprinus carpio var

A feeding trial was conducted to evaluate the results of replacing soybean meal (SBM) with other blend plant protein (BP) (rapeseed meal, cottonseed meal and peanut meal) sources on growth, fish body composition, biochemical parameters, non-specific immune index and gene expression of growth hormone/insulin-like growth factor-1 in Yellow River carp Cyprinus carpio. The results showed that the 600 g/kg replacement with BP in diet did not affect the growth performance of Yellow River carp, but the 800 g/kg SBM replacement diet could depress the growth of fish (p < .05). The 800 g/kg SBM replacement diet significantly impacted the superoxide dismutase, malondialdehyde contents, lysozyme, alanine aminotransferase and aspartate aminotransferase activities (p < .05). Fish fed 800 g/kg SBM replacement diet showed lowest insulin-like growth factor 1 and highest growth hormone level than that of other diets (p < .05). Both gene expression levels of GH and IGF-I in hepatic showed significant difference among dietary treatments (p < .05), and the lowest GH and IGF-I mRNA level in liver were found in fish fed 800 g/kg SBM replacement diet (p < .05). In conclusion, no more than 600 g/kg SBM could be replaced by BP in diet of Yellow River carp without adverse effects on the growth performance. However, 800 g/kg SBM replacement with BP in diet inhibited the growth performance, affected some blood parameters and immune response index, and down-regulated GH and IGF-1 gene expression of liver in Yellow River carp. Further, GH level in serum was negatively correlated with GH mRNA level in liver; meanwhile, serum concentrations of IGF-I were positively correlated with hepatic IGF-I mRNA expressions.

Evaluation of cysteamine supplementation in red tilapia (Oreochromis sp.) diet: Serum insulin and somatostatin, IGF-1 and GLUT4 genes expression, growth performance, and robustness against stress

The present study evaluated the effects of cysteamine supplementation on the serum insulin and somatostatin, IGF-1 and GLUT4 genes expression, growth performance and robustness against stress in red tilapia (Oreochromis sp.). This study tested five cysteamine dietary levels (quadruplicate), i.e. treatments consisted of control (N = 0 g/kg of cysteamine), A1 (0.25 g/kg cysteamine), A2 (0.50 g/kg of cysteamine), A3 (0.75 g/kg of cysteamine) and A4 (1.00 g/kg of cysteamine). All male red tilapia juvenile, with an average body weight of 6.98 ± 0.06 g, were kept in an aquarium (100 cm × 50 cm × 50 cm) previously filled with 175 L filtered water at the density of 12 fish/aquarium. Experimental diet was fed to the fish to satiation 3 times a day for 56 days rearing period. Stress challenge test was carried out by using air exposure technique. The results showed that final body weight, feed conversion ratio (FCR), protein retention and muscle protein significantly increased (P < .05) in response to cysteamine supplementation. Polynomial orthogonal contrast analysis demonstrated that the quadratic model regression of cysteamine supplementation level for specific growth rate (SGR) is y = 58.67 × 2 + 6.9317× + 3.7973 (P = .01) with an optimum level of 0.59 g/kg of cysteamine in the diet. Optimum cysteamine supplementation resulted in reduced blood glucose, protein and triglyceride blood levels (P < .05), indicating non protein energy utilization. Plasma somatostatin levels decreased along with the increase of cysteamine supplementation. IGF-1 and Glut4 genes expression in the liver significantly upregulated (P < .05) with cysteamine supplementation. In addition, cysteamine supplementation improved the fish robustness against stress, as indicated by increased superoxide dismutase (SOD), higher post-challenge survival and lower plasma cortisol, malondialdehyde (MDA) and glucose levels (P < .05). In conclusion, optimum cysteamine supplementation (0.59 g/kg) improved growth performance and robustness against stress in red tilapia.

The effect of Pediococcus acidilactici MA 18/5M on immune responses and mRNA levels of growth, antioxidant and immune-related genes in zebrafish (Danio rerio)

This study investigated the influence of probiotic Pediococcus acidilactici MA 18/5 M on the metabolic enzyme activities and mRNA levels of growth, immunity, and antioxidative-related genes in zebrafish. Zebrafish fed with diets containing P. acidilactici MA 18/5 M at 0, 107, 108, and 109 CFU/g levels for eight weeks. The obtained results revealed that the creatine phosphokinase, lactate dehydrogenase, alkaline phosphatase, alanine aminotransferase, and aspartate aminotransferase remained unchanged in all groups (P > 0.05). Dietary P. acidilactici enhanced protease activity relative to the control group (P < 0.05). Compared with the non-treated group, lysozyme activity increased in fish fed with high and medium doses of P. acidilactici, but the mRNA level of lysozyme gene was only up-regulated in the fish received the high dose of P. acidilactici (P < 0.05). Meanwhile, gene expressions of IGF-1, TNF-α, GH-1, and catalase were increased by P. acidilactici at 107 CFU/g relative to the control group. Conversely, the expression of glutathione S-reductase (GSR) decreased in zebrafish fed with medium and high doses of P. acidilactici compared to the control group. Thus, dietary administration of P. acidilactici MA 18/5 M, especially at 107 CFU/g diet, could improve the growth, immunity, and health status of zebrafish.

Using of betaine to replace fish meal with soybean or/and corn gluten meal in nile tilapia (Oreochromis niloticus) diets: Histomorphology, growth, fatty acid, and glucose-related gene expression traits

The present study was conducted to replace fish meal with alternative plant protein sources in aquafeeds. Therefore, soybean meal (SBM), corn gluten meal (CGM), and mix of SBM + CGM were used as alternatives to fish meal (FM) with or without betaine (B) in Nile tilapia diets. Positive control diet using FM and six other diets were formulated to contain SBM, SBM + B, CGM, CGM + B, SBM + CGM, or SBM + CGM + B. Dietary B improved fish growth and body protein content in comparison to the control and equal to fish fed FM-based diet. Reduced FCR and body fat content were observed in the case of fish fed FM, SBM + B, CGM + B, or SBM + CGM + B diets. The survival rate was significantly increased in the group of fish fed SBM + CGM + B when compared to fish fed CGM diet (P = 0.013) while no significant differences were reported among the other groups (P > 0.05). Markedly increased intestinal villi length and the number of goblet cells were found in FM, SBM+B, CGM+B, and SBM+CGM+B groups (P < 0.05). Hemoglobin, blood total protein, and IGF-1 gene expression were significantly (P < 0.05) increased in fish fed FM, CGM+B, SBM+CGM, and SBM+CGM+B diets, while fatty acid synthetase (FAS) and lipoprotein lipase (LPL) were downregulated. The highest RBCs, WBCs, and globulin were observed in fish fed SBM + CGM + B diet, while the lowest number was found in the fish fed CGM diet. To sum up, B supplementation in tilapia diets acted synergistically with SBM, CGM, or both SBM + CGM to improve the growth, intestinal morphometrical indices, hemoglobin, and total protein and IGF-1 as well as decreased FCR, FAS, and LPL.

Gene expression in human mesenchymal stem cell aging cultures: modulation by short peptides.

Effects of the short peptides Ala-Glu-Asp (AED), Lys-Glu-Asp (KED) and Lys-Glu (KE) on the expression of IGF1, FOXO1, TERT, TNKS2, and NFκB genes were studied in human embryo bone marrow mesenchymal stem cells (line FetMSCs) variously aged in "passages" or "stationary" cultures. Both cell aging models were similar in gene expression. The main difference was in the TERT gene expression level, which showed an eightfold increase at the "stationary" aging. IGF1 gene expression levels were very similar in both cell culture aging models, being enhanced by 3.5-5.6 fold upon the addition of the peptides. The FOXO1 gene was expressed twice more actively in the "stationary" than in the "passages" aging model. KED peptide inhibited FOXO1 gene expression by 1.6-2.3 fold. KE peptide increased FOXO1 gene expression by about two-fold in the "stationary" aging model but did not affect it in the "passage" aging model. The most striking difference in the peptide effect on cell aging between "passages" and "stationary" aging models was in the KED effects on TNKS2 gene expression; this expression was inhibited by KED in the "passages" model, while stimulation was observed in the "stationary" model. AED, KED, and KE stimulated expression of the NFκB gene in both models. Thus, the peptides studied at nanomolar concentrations modulate the expression of some genes known to be involved in cell aging.

Influence of the photoperiod and light intensity on growth performance, Melatonin and Insulin-like growth factors gene expression on Acipenser persicus during the embryonic stage

The effects of different light regimes (24L: 0D, 150 lux, 12L: 12D, 300lux, 0L: 24D, 0 lux, and control treatment) on growth, melatonin concentration, and Insulin-like growth factors gene expression of Persian sturgeon (Acipenser persicus) embryos were evaluated. Four groups of Persian sturgeon eggs (450 g) were incubated in Youshchenkov[X1] incubators with three replications for each treatment. The experiment was conducted during an 8- day period of incubation. Growth rate, plasma melatonin levels, and IGF-growth factors were investigated at 1, 4, and 8 days post fertilization. Results showed that higher mean weights growth were observed in fertilized eggs exposed to a 24L: 0D photoperiod with 150lux light intensity (p<0.05). The larval body length and hatching rate of fertilized eggs were significantly higher in embryos incubated at 12L: 12D with 300lux. The melatonin hormone level between sampling days and treatments were significantly different and it would be concluded that it may be related to the species. During the first-day post fertilization, the IGF-I and IGF-IR gene expression were significantly higher than other days. However, IGF-I and IGF-IR gene expression at different treatments showed no significant difference at day 4 and 8 post fertilization. According to the results, the stimulating role of IGF-I and IGF-IR gene expression in growth at the one-day post fertilization under different light regimes can be concluded. These findings suggest that the 12L:12D photoperiod with 300lux light intensity is the appropriate light regime for Persian sturgeon eggs incubation. The results of the present study would provide fundamental information for further use of light regimes during the early development of sturgeon larvae to optimize rearing protocols in sturgeon hatcheries.

Effect of 10 Weeks of Continuous Aerobic Training on Tumor Volume and Gene Expression of IGF-1, Akt, and mTORC1 in the Myocardium of Mice with Breast Cancer

Effect of 10 Weeks of Continuous Aerobic Training on Tumor Volume and Gene Expression of IGF-1, Akt, and mTORC1 in the Myocardium of Mice with Breast Cancer

Effect of amino acids on IGF1 gene expression in human myotubes and skeletal muscle

ObjectiveInsulin-like growth factor I (IGF1) is an important regulator of collagen and extracellular matrix protein expression. We aimed to evaluate the effect of amino acids (AAs) on expression of IGF1 and IGF1-dependent genes in human myotubes and skeletal muscle and supposed that AAs administration increases IGF1 levels in blood and expression of IGF1 and IGF1-dependent genes in trained skeletal muscle, thereby reducing training-induced muscle damage. DesignHuman myotubes were incubated with Arg and Leu for 24 h. Then, the effects of long-term branched chain AAs administration (10 weeks, 0.1 g/kg body mass/day) to volunteers (six subjects per AAs and placebo groups) performing large training volumes regularly (cross country skiers, training twice a day) were examined. ResultsIncubating the myotubes with AAs increases expression of IGF1 mRNA isoforms and IGF1 secretion by 2–3 times. In athletes, long-term AAs administration increased basal blood levels of IGF1 (~50%) and expression of IGF1Ea mRNA slightly in skeletal muscle. There is no marked increase in expression of COL1A1, COL3A1, COL5A1, and LOX genes in skeletal muscle after AAs administration. However, expression of these genes in the combined group (placebo + AAs; n = 12) significantly correlated with the expression of IGF1Ea mRNA in muscle and did not correlate with IGF1 levels in the blood. ConclusionsAAs administration increases IGF1 expression in vitro and in vivo. To obtain more pronounced changes in expression of IGF1 and IGF1-dependent genes in skeletal muscle, it may be necessary to increase the dose and/or duration of AAs administration.