The effect of dietary Crataegus Sinaica on the growth performance, immune responses, hemato-biochemical and oxidative stress indices, tissues architecture, and resistance to Aeromonas sobria infection of acrylamide-exposed Clarias gariepinus

[1]  T. M. Saber,et al.  Alleviative effects of dietary Silybum marianum and co-enzyme Q10 on waterborne nickel-induced impaired growth, immunosuppression, tissue damage, immune-related genes dysregulation, and reduced resistance to Pseudomonas aeruginosa in Oreochromis niloticus , 2022, Aquaculture Reports.

[2]  I. Alsharif,et al.  Crataegus sinaica defatted methanolic extract ameliorated monosodium iodoacetate-induced oxidative stress andinhibited inflammation in a rat model of osteoarthritis , 2022, Research in pharmaceutical sciences.

[3]  F. Erkoç,et al.  Sublethal effects of acrylamide on thyroid hormones, complete blood count and micronucleus frequency of vertebrate model organism (Cyprinus carpio) , 2022, Turkish Journal of Biochemistry.

[4]  M. Metwally,et al.  Dietary Parsley Seed Mitigates Methomyl-Induced Impaired Growth Performance, Hemato-Immune Suppression, Oxidative Stress, Hepato-Renal Damage, and Pseudomonas aeruginosa Susceptibility in Oreochromis niloticus , 2022, Antioxidants.

[5]  A. Uçar,et al.  Borax relieved the acrylamide-induced hematotoxic, hepatotoxic, immunotoxic and genotoxic damages in rainbow trout by regulating apoptosis and Nrf2 signaling pathway. , 2022, Comparative biochemistry and physiology. Toxicology & pharmacology : CBP.

[6]  H. Park,et al.  High cortisol levels are associated with oxidative stress and mortality in maintenance hemodialysis patients , 2022, BMC Nephrology.

[7]  Walaa El-Houseiny,et al.  Milk thistle and co-enzyme Q10 fortified diets lessen the nickel chloride-induced neurotoxic and neurobehavioral impairments in Oreochromis niloticus via regulating the oxidative stress response, acetylcholinesterase activity, and brain nickel content , 2022, Aquaculture.

[8]  O. Pardo,et al.  Review of the state of the art of acrylamide human biomonitoring. , 2022, Chemosphere.

[9]  M. F. Madkour Hassan,et al.  The Anti-Inflammatory, Anti-Apoptotic, and Antioxidant Effects of a Pomegranate-Peel Extract against Acrylamide-Induced Hepatotoxicity in Rats , 2022, Life.

[10]  K. Abo-El-Sooud,et al.  The impact of long-term oral exposure to low doses of acrylamide on the hematological indicators, immune functions, and splenic tissue architecture in rats. , 2022, International immunopharmacology.

[11]  X. Xia,et al.  Dietary Acrylamide Intake Alters Gut Microbiota in Mice and Increases Its Susceptibility to Salmonella Typhimurium Infection , 2021, Foods.

[12]  M. Metwally,et al.  The single or combined Silybum marianum and co-enzyme Q10 role in alleviating fluoride-induced impaired growth, immune suppression, oxidative stress, histological alterations, and reduced resistance to Aeromonas sobria in African catfish (Clarias gariepinus) , 2021, Aquaculture.

[13]  Ana Paula da Fonseca Machado,et al.  Chemoprevention with a tea from hawthorn (Crataegus oxyacantha) leaves and flowers attenuates colitis in rats by reducing inflammation and oxidative stress , 2021, Food chemistry: X.

[14]  F. Bedir,et al.  Protective effect of taxifolin against prooxidant and proinflammatory kidney damage associated with acrylamide in rats. , 2021, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

[15]  N. Saenen,et al.  Gestational acrylamide exposure and biomarkers of fetal growth: Probing the mechanism underlying the association between acrylamide and reduced fetal growth. , 2021, Environment international.

[16]  J. Verreth,et al.  Quantifying methionine requirement of juvenile African catfish (Clarias gariepinus) , 2021 .

[17]  J. Ogunji,et al.  Alternative protein source: Acceptability of cow blood meal in place of fish meal assessed via growth, antioxidant enzymes functions and haematological response in Clarias gariepinus (Burchell, 1822) , 2021 .

[18]  Jun Wang,et al.  The adverse effects of acrylamide exposure on the early development of marine medaka (Oryzias melastigma) and its mechanisms. , 2021, Marine pollution bulletin.

[19]  A. Amin,et al.  Hawthorn Herbal Preparation from Crataegus oxyacantha Attenuates In Vivo Carbon Tetrachloride -Induced Hepatic Fibrosis via Modulating Oxidative Stress and Inflammation , 2020, Antioxidants.

[20]  M. Abdollahi,et al.  Oral Administration of Acrylamide Worsens the Inflammatory Responses in the Airways of Asthmatic Mice Through Agitation of Oxidative Stress in the Lungs , 2020, Frontiers in Immunology.

[21]  Gembu Abe,et al.  Assessing effects of substituting dietary fish meal with boiled donkey and cow blood meal on growth performance and digestive enzyme activities of Clarias gariepinus juvenile , 2020 .

[22]  M. Matsuoka,et al.  Intake of acrylamide at the dietary relevant concentration causes splenic toxicity in adult zebrafish. , 2020, Environmental research.

[23]  T. Liu,et al.  Protective effect of seabuckthorn berry juice against acrylamide-induced oxidative damage in rats. , 2020, Journal of food science.

[24]  R. Ahmed,et al.  Stigmasterol protects rats from collagen induced arthritis by inhibiting proinflammatory cytokines. , 2020, International immunopharmacology.

[25]  O. A. El-Shahaby,et al.  Green Synthesis and Biological Assessments of Silver Nanoparticles Using the Plant Extract of Crataegus sinaica Boiss. Fruits , 2020 .

[26]  Yanhua Huang,et al.  Effects of dietary hawthorn extracts supplementation on lipid metabolism, skin coloration and gut health of golden pompano (Trachinotus ovatus) , 2020 .

[27]  S. Iheanacho,et al.  Neurotoxicity, oxidative stress biomarkers and haematological responses in African catfish (Clarias gariepinus) exposed to polyvinyl chloride microparticles. , 2020, Comparative biochemistry and physiology. Toxicology & pharmacology : CBP.

[28]  N. Schreurs,et al.  Flavonoid bioactive compounds of hawthorn extract can promote growth, regulate electrocardiogram waves, and improve cardiac parameters of pulmonary hypertensive chickens , 2019, Poultry science.

[29]  N. Ziada.  THERAPEUTIC EFFECT OF CRATAEGUS SINAICA FRUIT ON VASCULAR DISEASES IN MALE RABBITS , 2020 .

[30]  M. Ibrahim,et al.  Acrylamide‐induced hematotoxicity, oxidative stress, and DNA damage in liver, kidney, and brain of catfish (Clarias gariepinus) , 2020, Environmental toxicology.

[31]  A. Kucharska,et al.  Hawthorn (Crataegus monogyna) Phenolic Extract Modulates Lymphocyte Subsets and Humoral Immune Response in Mice , 2019, Planta Medica.

[32]  Gang Li,et al.  Hawthorne leaf flavonoids prevent oxidative stress injury of renal tissues in rats with diabetic kidney disease by regulating the p38 MAPK signaling pathway. , 2019, International journal of clinical and experimental pathology.

[33]  M. Matsuoka,et al.  In vitro and in vivo studies of oxidative stress responses against acrylamide toxicity in zebrafish. , 2019, Journal of hazardous materials.

[34]  M. Benali,et al.  Effect of oral exposure to acrylamide on biochemical and hematologic parameters in Wistar rats , 2019, Drug and chemical toxicology.

[35]  Jian Wang,et al.  Effect of acrylamide on glucose homeostasis in female rats and its mechanisms. , 2019, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[36]  X. Shu,et al.  Carnosic acid attenuates acrylamide‐induced retinal toxicity in zebrafish embryos , 2018, Experimental eye research.

[37]  Mengmeng Huang,et al.  Characterization of acrylamide-induced oxidative stress and cardiovascular toxicity in zebrafish embryos. , 2018, Journal of hazardous materials.

[38]  Mengmeng Huang,et al.  Exposure to acrylamide induces cardiac developmental toxicity in zebrafish during cardiogenesis. , 2018, Environmental pollution.

[39]  Abdelmonem Awad Hegazy.  Effect of Administration of Acrylamide and Possible Protective Role of Vitamin E on Postnatal Rat Liver Structure , 2018 .

[40]  A. Cebi,et al.  Acrylamide in Environmental Water: A Review on Sources, Exposure, and Public Health Risks , 2019, Exposure and Health.

[41]  S. M. Hosseini,et al.  Hawthorn (Crataegus Oxyacantha) Extract in the Drinking Water of Broilers on Growth and Incidence of Pulmonary Hypertension Syndrome (PHS) , 2017 .

[42]  Xiaohong Tan,et al.  Effects of dietary hawthorn extract on growth performance, immune responses, growth‐ and immune‐related genes expression of juvenile golden pompano (Trachinotus ovatus) and its susceptibility to Vibrio harveyi infection , 2017, Fish & shellfish immunology.

[43]  Birsen Aydın,et al.  Argan oil reduces oxidative stress, genetic damage and emperipolesis in rats treated with acrylamide. , 2017, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

[44]  S. Abediankenari,et al.  Acrylamide induces immunotoxicity through reactive oxygen species production and caspase-dependent apoptosis in mice splenocytes via the mitochondria-dependent signaling pathways. , 2017, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

[45]  C. Chen,et al.  Hypoglycemic effect of hawthorn in type II diabetes mellitus rat model. , 2017, The Journal of the Science of Food and Agriculture.

[46]  Zeghal Najiba,et al.  Extra Virgin olive oil mitigates hematotoxicity induced by acrylamide and oxidative damage in adult rats , 2017 .

[47]  T. Su,et al.  Negative association between acrylamide exposure and body composition in adults: NHANES, 2003–2004 , 2017, Nutrition & diabetes.

[48]  N. Zeghal,et al.  Olive oil abrogates acrylamide induced nephrotoxicity by modulating biochemical and histological changes in rats , 2016, Renal failure.

[49]  Xingbin Yang,et al.  Polyphenols from hawthorn peels and fleshes differently mitigate dyslipidemia, inflammation and oxidative stress in association with modulation of liver injury in high fructose diet-fed mice. , 2016, Chemico-biological interactions.

[50]  Seyyed Morteza Hoseini,et al.  Serum cortisol, glucose, thyroid hormones' and non-specific immune responses of Persian sturgeon, Acipenser persicus to exogenous tryptophan and acute stress , 2016 .

[51]  O. S. Oluwagbemiga,et al.  The Growth Performance of African Catfish ( Clarias gariepinus ) Fed Commercially Prepared Imported Fish Feeds , 2016 .

[52]  Pancreatic lipase and α-amylase inhibitory activities of plants used in Traditional Chinese Medicine (TCM). , 2016, Die Pharmazie.

[53]  L. Chekir‐Ghedira,et al.  Immunomodulatory potencies of isolated compounds from Crataegus azarolus through their antioxidant activities , 2016, Tumor Biology.

[54]  Yue Wang,et al.  A urinary metabolomics study of rats after the exposure to acrylamide by ultra performance liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry. , 2015, Molecular bioSystems.

[55]  P. Baptista,et al.  Histopathological findings on Carassius auratus hepatopancreas upon exposure to acrylamide: correlation with genotoxicity and metabolic alterations , 2014, Journal of applied toxicology : JAT.

[56]  G. Shao,et al.  Mycoplasma hyopneumoniae-derived lipid-associated membrane proteins induce apoptosis in porcine alveolar macrophage via increasing nitric oxide production, oxidative stress, and caspase-3 activation. , 2013, Veterinary immunology and immunopathology.

[57]  A. Nematollahi,et al.  Effects of cadmium at sub-lethal concentration on growth and biochemical parameters in rainbow trout (Oncorhynchus mykiss) , 2013, Irish Veterinary Journal.

[58]  P. Cole,et al.  Evaluation of the national toxicology program report on carcinogens. , 2012, Regulatory toxicology and pharmacology : RTP.

[59]  S. Panserat,et al.  Glucose metabolism in fish: a review , 2012, Journal of Comparative Physiology B.

[60]  R. Fagard,et al.  Stimulation of reactive oxygen species and collagen synthesis by angiotensin II in cardiac fibroblasts. , 2012, Cardiovascular therapeutics.

[61]  G. Piccione,et al.  Automatic analysis to assess haematological parameters in farmed gilthead sea bream (Sparus aurata Linnaeus, 1758) , 2012 .

[62]  K. Kamala,et al.  Toxic Effect of Acrylamide on Body Weight, the Study of Antioxidants and Histoarchitecture of Heart in the Developing Chick Embryo , 2011 .

[63]  L. Knudsen,et al.  Analysis of hemoglobin adducts from acrylamide, glycidamide, and ethylene oxide in paired mother/cord blood samples from Denmark. , 2011, Chemical research in toxicology.

[64]  Q. Gao,et al.  Two flavanone compounds from litchi (Litchi chinensis Sonn.) seeds, one previously unreported, and appraisal of their α-glucosidase inhibitory activities , 2011 .

[65]  Fan Zhou,et al.  Partial Replacement of Fish Meal by Fermented Soybean Meal in Diets for Black Sea Bream, Acanthopagrus schlegelii, Juveniles , 2011 .

[66]  Ana Maria Carvalho,et al.  Comparing the composition and bioactivity of Crataegus Monogyna flowers and fruits used in folk medicine. , 2011, Phytochemical analysis : PCA.

[67]  Hitomi Hayashi,et al.  Disruptive neuronal development by acrylamide in the hippocampal dentate hilus after developmental exposure in rats , 2011, Archives of Toxicology.

[68]  N. Yassin,et al.  Phytochemical and biological activities of Crataegus sinaica growing in Egypt. , 2010 .

[69]  Hao Wang,et al.  Reproductive toxicity of acrylamide-treated male rats. , 2010, Reproductive toxicology.

[70]  E. Scheidegger,et al.  RFLP analysis of a PCR-amplified fragment of the 16S rRNA gene as a tool to identify Enterococcus strains. , 2009, Memorias do Instituto Oswaldo Cruz.

[71]  H. Kuo,et al.  Association Among Acrylamide, Blood Insulin, and Insulin Resistance in Adults , 2009, Diabetes Care.

[72]  Rong Tsao,et al.  Screening and structural characterization of α-glucosidase inhibitors from hawthorn leaf flavonoids extract by ultrafiltration LC-DAD-MSn and SORI-CID FTICR MS , 2009, Journal of the American Society for Mass Spectrometry.

[73]  B. Ji,et al.  Evaluation of antioxidative and hypolipidemic properties of a novel functional diet formulation of Auricularia auricula and Hawthorn , 2009 .

[74]  M. Andrew Stamper,et al.  Fish Sedation, Anesthesia, Analgesia, and Euthanasia: Considerations, Methods, and Types of Drugs , 2009 .

[75]  M. Lydy,et al.  Toxicity of anionic polyacrylamide formulations when used for erosion control in agriculture. , 2009, Journal of environmental quality.

[76]  S. El-Assouli.  Acrylamide in selected foods and genotoxicity of their extracts. , 2009, The Journal of the Egyptian Public Health Association.

[77]  P. Xie,et al.  Changes in plasma thyroid hormones and cortisol levels in crucian carp (Carassius auratus) exposed to the extracted microcystins. , 2008, Chemosphere.

[78]  N. Menković,et al.  Anti-inflammatory, gastroprotective, free-radical-scavenging, and antimicrobial activities of hawthorn berries ethanol extract. , 2008, Journal of agricultural and food chemistry.

[79]  F. Clavel-Chapelon,et al.  Cross-sectional study on acrylamide hemoglobin adducts in subpopulations from the European Prospective Investigation into Cancer and Nutrition (EPIC) Study. , 2008, Journal of agricultural and food chemistry.

[80]  E. Stackebrandt,et al.  Aeromonas aquariorum sp. nov., isolated from aquaria of ornamental fish. , 2008, International journal of systematic and evolutionary microbiology.

[81]  R. Borski,et al.  Endocrine Biomarkers of Growth and Applications to Aquaculture: A Minireview of Growth Hormone, Insulin‐Like Growth Factor (IGF)‐I, and IGF‐Binding Proteins as Potential Growth Indicators in Fish , 2008 .

[82]  W. Bajdur.  Application of acrylamide polymers as flocculants in sewages coagulation process , 2008 .

[83]  Young A Lee,et al.  Ameliorative effects of proanthocyanidin on oxidative stress and inflammation in streptozotocin-induced diabetic rats. , 2007, Journal of agricultural and food chemistry.

[84]  M. Paule,et al.  Effects of chronic low-dose acrylamide exposure on progressive ratio performance in adolescent rats. , 2007, Neurotoxicology.

[85]  A. Kozińska.  Dominant pathogenic species of mesophilic aeromonads isolated from diseased and healthy fish cultured in Poland. , 2007, Journal of fish diseases.

[86]  M. M. Tarskikh.  Damage to erythrocyte membranes as the mechanism for acrylate toxicity , 2006, Bulletin of Experimental Biology and Medicine.

[87]  K. Engin,et al.  The Effects of Cadmium on Levels of Glucose in Serum and Glycogen Reserves in the Liver and Muscle Tissues of Cyprinus carpio (L., 1758) , 2005 .

[88]  T. Tseng,et al.  Anti-inflammatory potential of flavonoid contents from dried fruit of Crataegus pinnatifida in vitro and in vivo. , 2005, Journal of agricultural and food chemistry.

[89]  J. Błasiak,et al.  Genotoxicity of acrylamide in human lymphocytes. , 2004, Chemico-biological interactions.

[90]  J. Miwa,et al.  Extremely low dose of acrylamide decreases lifespan in Caenorhabditis elegans. , 2004, Toxicology letters.

[91]  M. Claeys,et al.  Antiviral and antioxidant activity of flavonoids and proanthocyanidins from Crataegus sinaica. , 2002, Planta medica.

[92]  P. Delves,et al.  The Immune System , 2000 .

[93]  Michael E. McManus,et al.  Some industrial chemicals , 2000 .

[94]  H. Pratap,et al.  Effects of water-borne cadmium on plasma cortisol and glucose in the cichlid fish Oreochromis mossambicus , 1990 .

[95]  H. Aebi,et al.  Catalase in vitro. , 1984, Methods in enzymology.

[96]  G. Berti,et al.  Enzymic creatinine assay: a new colorimetric method based on hydrogen peroxide measurement. , 1983, Clinical chemistry.

[97]  M. Uchiyama,et al.  Determination of malonaldehyde precursor in tissues by thiobarbituric acid test. , 1978, Analytical biochemistry.

[98]  K. Yagi,et al.  The occurrence of superoxide anion in the reaction of reduced phenazine methosulfate and molecular oxygen. , 1972, Biochemical and biophysical research communications.

[99]  M. Kaplan.  Alkaline phosphatase. , 1972, Gastroenterology.

[100]  H. Badawi.  Electrophoretic studies of serum proteins of four Tilapia species (Pisces) , 1971 .

[101]  M. Walters,et al.  An ultramicromethod for the determination of conjugated and total bilirubin in serum or plasma , 1970 .

[102]  W. Valentine,et al.  Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. , 1967, The Journal of laboratory and clinical medicine.