Dietary dihydroartemisinin supplementation alleviates intestinal inflammatory injury through TLR4/NOD/NF-κB signaling pathway in weaned piglets with intrauterine growth retardation
暂无分享,去创建一个
Yongwei Zhao | Lili Zhang | Tian Wang | Z. Gan | Y. Niu | M. Shen | Jintian He | Yang Yun | Zhending Gan
[1] H. Geng,et al. Cell death of intestinal epithelial cells in intestinal diseases. , 2020, Sheng li xue bao : [Acta physiologica Sinica].
[2] Yuan-Jian Song,et al. Dihydroartemisinin ameliorates LPS-induced neuroinflammation by inhibiting the PI3K/AKT pathway , 2020, Metabolic Brain Disease.
[3] Jian Li,et al. Microbial insight into dietary protein source affects intestinal function of pigs with intrauterine growth retardation , 2020, European journal of nutrition.
[4] Ying Hu,et al. Co-Delivery Of Dihydroartemisinin And HMGB1 siRNA By TAT-Modified Cationic Liposomes Through The TLR4 Signaling Pathway For Treatment Of Lupus Nephritis , 2019, International journal of nanomedicine.
[5] Y. Yamanashi,et al. Loss of C/EBPδ enhances apoptosis of intestinal epithelial cells and exacerbates experimental colitis in mice , 2019, Genes to cells : devoted to molecular & cellular mechanisms.
[6] Ji-Hua Liu,et al. Dihydroartemisinin derivative DC32 inhibits inflammatory response in osteoarthritic synovium through regulating Nrf2/NF-κB pathway. , 2019, International immunopharmacology.
[7] Shimeng Huang,et al. Characteristics of the gut microbiota colonization, inflammatory profile, and plasma metabolome in intrauterine growth restricted piglets during the first 12 hours after birth , 2019, Journal of Microbiology.
[8] Yulong Yin,et al. Effects of dietary lysozyme levels on growth performance, intestinal morphology, immunity response and microbiota community of growing pigs. , 2018, Journal of the science of food and agriculture.
[9] Jingfei Zhang,et al. Dietary curcumin supplementation attenuates inflammation, hepatic injury and oxidative damage in a rat model of intra-uterine growth retardation , 2018, British Journal of Nutrition.
[10] Yongqing Hou,et al. Glycine Relieves Intestinal Injury by Maintaining mTOR Signaling and Suppressing AMPK, TLR4, and NOD Signaling in Weaned Piglets after Lipopolysaccharide Challenge , 2018, International journal of molecular sciences.
[11] Zhanjun Jia,et al. Role of dihydroartemisinin in regulating prostaglandin E2 synthesis cascade and inflammation in endothelial cells , 2018, Heart and Vessels.
[12] H. Zhang,et al. Effects of dietary Bacillus amyloliquefaciens supplementation on growth performance, intestinal morphology, inflammatory response, and microbiota of intra-uterine growth retarded weanling piglets , 2018, Journal of Animal Science and Biotechnology.
[13] Z. Ying,et al. Effects of dietary l-methionine supplementation on intestinal integrity and oxidative status in intrauterine growth-retarded weanling piglets , 2018, European Journal of Nutrition.
[14] Honggang Zhou,et al. Dihydroartemisinin attenuates autoimmune thyroiditis by inhibiting the CXCR3/PI3K/AKT/NF-κB signaling pathway , 2017, Oncotarget.
[15] A. Mouihate,et al. Dexamethasone-Induced Intrauterine Growth Restriction Is Associated With Altered Expressions of Metastasis Tumor Antigens and Cell Cycle Control Proteins in Rat Placentas , 2017, Reproductive Sciences.
[16] Lili Zhang,et al. Effects of medium-chain triglycerides on intestinal morphology and energy metabolism of intrauterine growth retarded weanling piglets , 2017, Archives of animal nutrition.
[17] Xiuying Wang,et al. Aspartate attenuates intestinal injury and inhibits TLR4 and NODs/NF-κB and p38 signaling in weaned pigs after LPS challenge , 2017, European Journal of Nutrition.
[18] Libo Jiang,et al. Dihydroartemisinin inhibits catabolism in rat chondrocytes by activating autophagy via inhibition of the NF-κB pathway , 2016, Scientific Reports.
[19] L. Tenenbaum,et al. Tollip, an early regulator of the acute inflammatory response in the substantia nigra , 2016, Journal of Neuroinflammation.
[20] Lili Zhang,et al. Supplementation of tributyrin improves the growth and intestinal digestive and barrier functions in intrauterine growth-restricted piglets. , 2016, Clinical nutrition.
[21] S. Mcelroy,et al. Intrauterine Growth Restriction Alters Mouse Intestinal Architecture during Development , 2016, PloS one.
[22] Li-guang Shi,et al. Effects of curcumin on growth performance, jejunal mucosal membrane integrity, morphology and immune status in weaned piglets challenged with enterotoxigenic Escherichia coli. , 2015, International immunopharmacology.
[23] Dongxia Yang,et al. Dihydroartemisinin supresses inflammation and fibrosis in bleomycine-induced pulmonary fibrosis in rats. , 2015, International journal of clinical and experimental pathology.
[24] H. Peh,et al. Artemisinins: pharmacological actions beyond anti-malarial. , 2014, Pharmacology & therapeutics.
[25] H. Anders,et al. Pattern-Recognition Receptor Signaling Regulator mRNA Expression in Humans and Mice, and in Transient Inflammation or Progressive Fibrosis , 2013, International journal of molecular sciences.
[26] Qing-Wu Yang,et al. Toll-like receptor 4 signaling in intracerebral hemorrhage-induced inflammation and injury , 2013, Journal of Neuroinflammation.
[27] M. Stronati,et al. Short-term and long-term sequelae in intrauterine growth retardation (IUGR) , 2013, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.
[28] Wen‐bin Liu,et al. Dietary L-arginine supplementation improves the intestinal development through increasing mucosal Akt and mammalian target of rapamycin signals in intra-uterine growth retarded piglets. , 2012, The British journal of nutrition.
[29] I. Connerton,et al. Campylobacter jejuni activates NF-kappaB independently of TLR2, TLR4, Nod1 and Nod2 receptors. , 2010, Microbial pathogenesis.
[30] I. Le Huërou-Luron,et al. Intrauterine growth restriction modifies the developmental pattern of intestinal structure, transcriptomic profile, and bacterial colonization in neonatal pigs. , 2010, The Journal of nutrition.
[31] T. Lawrence. The nuclear factor NF-kappaB pathway in inflammation. , 2009, Cold Spring Harbor perspectives in biology.
[32] T. Lawrence. The Nuclear Factor NF-kB Pathway in Inflammation , 2009 .
[33] Guoyao Wu,et al. Intrauterine growth restriction affects the proteomes of the small intestine, liver, and skeletal muscle in newborn pigs. , 2008, The Journal of nutrition.
[34] Gabriel Núñez,et al. Intracellular NOD-like receptors in host defense and disease. , 2007, Immunity.
[35] W. Walker,et al. TLRs in the Gut I. The role of TLRs/Nods in intestinal development and homeostasis. , 2007, American journal of physiology. Gastrointestinal and liver physiology.
[36] D. Philpott,et al. Nod-like proteins in immunity, inflammation and disease , 2006, Nature Immunology.
[37] Guoyao Wu,et al. Board-invited review: intrauterine growth retardation: implications for the animal sciences. , 2006, Journal of animal science.
[38] T. Buchmiller,et al. Effect of Esophageal Ligation on Small Intestinal Development in Normal and Growth-retarded Fetal Rabbits , 2006, Journal of pediatric gastroenterology and nutrition.
[39] Y. Tu,et al. Dihydroarteannuin ameliorates lupus symptom of BXSB mice by inhibiting production of TNF-alpha and blocking the signaling pathway NF-kappa B translocation. , 2006, International immunopharmacology.
[40] P. Lécine,et al. A Role for Erbin in the Regulation of Nod2-dependent NF-κB Signaling* , 2005, Journal of Biological Chemistry.
[41] F. Shi,et al. Effects of Intrauterine Growth Retardation on Development of the Gastrointestinal Tract in Neonatal Pigs , 2005, Neonatology.
[42] A. Tarakhovsky,et al. Negative regulation of Toll-like receptor 4 signaling by the Toll-like receptor homolog RP105 , 2005, Nature Immunology.
[43] Jeffrey S. Robinson,et al. Developmental origins of the metabolic syndrome: prediction, plasticity, and programming. , 2005, Physiological reviews.
[44] E. Pålsson-McDermott,et al. Signal transduction by the lipopolysaccharide receptor, Toll‐like receptor‐4 , 2004, Immunology.
[45] J. Hsu,et al. Uteroplacental insufficiency decreases small intestine growth and alters apoptotic homeostasis in term intrauterine growth retarded rats. , 2004, Early human development.
[46] J. Thorp,et al. Intrauterine growth restriction increases morbidity and mortality among premature neonates. , 2004, American journal of obstetrics and gynecology.
[47] J. Hsu,et al. Uteroplacental insufficiency increases apoptosis and alters p53 gene methylation in the full-term IUGR rat kidney. , 2003, American journal of physiology. Regulatory, integrative and comparative physiology.
[48] S. Foster,et al. An essential role for NOD1 in host recognition of bacterial peptidoglycan containing diaminopimelic acid , 2003, Nature Immunology.
[49] M. Chamaillard,et al. Nod2 Is a General Sensor of Peptidoglycan through Muramyl Dipeptide (MDP) Detection* , 2003, The Journal of Biological Chemistry.
[50] M. Kubo,et al. SOCS1/JAB is a negative regulator of LPS-induced macrophage activation. , 2002, Immunity.
[51] A. Baldwin. Control of oncogenesis and cancer therapy resistance by the transcription factor NF-kappaB. , 2001, The Journal of clinical investigation.
[52] Johannes Gerdes,et al. The Ki‐67 protein: From the known and the unknown , 2000, Journal of cellular physiology.
[53] David M. Rothwarf,et al. The NF-κB Activation Pathway: A Paradigm in Information Transfer from Membrane to Nucleus , 1999, Science's STKE.
[54] A. Porter,et al. Emerging roles of caspase-3 in apoptosis , 1999, Cell Death and Differentiation.
[55] S. Saccani,et al. The Human Toll Signaling Pathway: Divergence of Nuclear Factor κB and JNK/SAPK Activation Upstream of Tumor Necrosis Factor Receptor–associated Factor 6 (TRAF6) , 1998, The Journal of experimental medicine.
[56] Z. Cao,et al. MyD88: an adapter that recruits IRAK to the IL-1 receptor complex. , 1997, Immunity.
[57] D. Baltimore,et al. NF-κB Activation: The IκB Kinase Revealed? , 1997, Cell.
[58] David M. Rothwarf,et al. A cytokine-responsive IκB kinase that activates the transcription factor NF-κB , 1997, Nature.
[59] D. Baltimore,et al. NF-kappaB activation: the I kappaB kinase revealed? , 1997, Cell.
[60] Zhaodan Cao,et al. TRAF6 is a signal transducer for interleukin-1 , 1996, Nature.
[61] T. Kirikae,et al. The chemical structure of bacterial endotoxin in relation to bioactivity. , 1993, Immunobiology.
[62] M. Bogdanffy,et al. Evaluation of proliferating cell nuclear antigen (PCNA) as an endogenous marker of cell proliferation in rat liver: a dual-stain comparison with 5-bromo-2'-deoxyuridine. , 1993, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.