5 results on '"Guang-Yin Xu"'
Search Results
2. Epigenetic upregulation of acid-sensing ion channel 1 contributes to gastric hypersensitivity in adult offspring rats with prenatal maternal stress
- Author
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Hong-Jun Wang, Meng Li, Xue Xu, Guang-Yin Xu, Yu-Cheng Xu, Ping-An Zhang, Xinghong Jiang, and You-Lang Zhou
- Subjects
medicine.medical_specialty ,Patch-Clamp Techniques ,Offspring ,Bisulfite sequencing ,Biology ,Epigenesis, Genetic ,03 medical and health sciences ,0302 clinical medicine ,Dorsal root ganglion ,Downregulation and upregulation ,030202 anesthesiology ,Pregnancy ,Stress, Physiological ,Internal medicine ,Ganglia, Spinal ,medicine ,Animals ,Epigenetics ,Acid-sensing ion channel ,Stomach ,Methylation ,Rats ,Up-Regulation ,Acid Sensing Ion Channels ,Anesthesiology and Pain Medicine ,medicine.anatomical_structure ,Endocrinology ,Neurology ,Female ,Neurology (clinical) ,Chromatin immunoprecipitation ,030217 neurology & neurosurgery - Abstract
Functional dyspepsia is a common functional gastrointestinal disorder. Gastric hypersensitivity (GHS) is a hallmark of this disorder, but the cellular mechanisms remain largely unknown. Stressors during gestational period could have effects on the offspring's tissue structure and function, which may predispose to gastrointestinal diseases. The aim of this study was to test whether prenatal maternal stress (PMS) induces GHS and to investigate role of acid-sensing ion channel (ASIC)/nuclear factor-κB (NF-κB) signaling by examining Asic1 methylation status in adult offspring rats. Gastric hypersensitivity in response to gastric distension was examined by electromyography recordings. Changes in neuronal excitability were determined by whole-cell patch-clamp recording techniques. Demethylation of CpG islands of Asic1 was determined by methylation-specific PCR and bisulfite sequencing assay. Prenatal maternal stress produced GHS in adult offspring rats. Treatment with amiloride, an inhibitor of ASICs, significantly attenuated GHS and reversed hyperexcitability of gastric-specific dorsal root ganglion (DRG) neurons labeled by the dye DiI. Expression of ASIC1 and NF-κBp65 was markedly enhanced in T7 to T10 DRGs. Furthermore, PMS led to a significant demethylation of CpG islands in the Asic1 promoter. A chromatin immunoprecipitation assay showed that PMS also enhanced the ability of NF-κBp65 to bind the promoter of Asic1 gene. Blockade of NF-κB using lentiviral-p65shRNA reversed upregulation of ASIC1 expression, GHS, and the hyperexcitability of DRG neurons. These data suggest that upregulation of ASIC1 expression is attributed to Asic1 promoter DNA demethylation and NF-κB activation, and that the enhanced interaction of the Asic1 and NF-κBp65 contributes to GHS induced by PMS.
- Published
- 2020
3. Enhanced binding capability of nuclear factor-κB with demethylated P2X3 receptor gene contributes to cancer pain in rats
- Author
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Shufen Hu, Guang-Yin Xu, Jinrong Wei, Xinghong Jiang, Wei Chen, Hong-Yan Zhu, Guo-Qin Jiang, Hong-Hong Zhang, and You-Lang Zhou
- Subjects
P2X3 receptors ,Action Potentials ,Rats, Sprague-Dawley ,chemistry.chemical_compound ,Dorsal root ganglion ,Pyrrolidine dithiocarbamate ,Ganglia, Spinal ,Sulfones ,Enzyme Inhibitors ,Receptor ,Neurons ,p65 ,Purinergic receptor ,NF-kappa B ,Long-term potentiation ,Cell biology ,medicine.anatomical_structure ,Neurology ,Hyperalgesia ,DNA demethylation ,Female ,Caner pain ,medicine.symptom ,Research Paper ,Protein Binding ,Pain Threshold ,medicine.medical_specialty ,Proline ,Pain ,Antineoplastic Agents ,Bone Neoplasms ,Methylation ,Downregulation and upregulation ,Thiocarbamates ,Internal medicine ,Nitriles ,medicine ,Animals ,Pain Management ,NFKB1 ,Rats ,body regions ,Disease Models, Animal ,Anesthesiology and Pain Medicine ,Endocrinology ,chemistry ,Case-Control Studies ,Neurology (clinical) ,Receptors, Purinergic P2X3 - Abstract
Supplemental Digital Content is Available in the Text. Epigenetic regulations of P2X3 receptors play a crucial role in cancer pain. Targeting p65 binding to demethylated P2X3 receptor gene suppresses cancer pain., Nuclear factor-kappa B (NF-κB) signaling is implicated in both cancer development and inflammation processes. However, the roles and mechanisms of NF-κB signaling in the development of cancer-induced pain (CIP) remain unknown. This study was designed to investigate the roles of the p65 subunit of NF-κB in regulation of the purinergic receptor (P2X3R) plasticity in dorsal root ganglion (DRG) of CIP rats. We showed here that tumor cell injection produced mechanical and thermal hyperalgesia, and an enhanced body weight–bearing difference, which was correlated with an upregulation of p65 and P2X3R expression in lumber DRGs and a potentiation of ATP-evoked responses of tibia-innervating DRG neurons. Inhibition of NF-κB signaling using p65 inhibitor pyrrolidine dithiocarbamate, BAY-11-7082, or lentiviral-p65 short-hairpin RNA significantly attenuated CIP and reversed the activities of P2X3R. Interestingly, tumor cell injection led to a significant demethylation of CpG island in p2x3r gene promoter and enhanced ability of p65 to bind the promoter of p2x3r gene. Our findings suggest that upregulation of P2X3R expression was mediated by the enhanced binding capability of p65 with demethylated promoter of p2x3r gene, thus contributing to CIP. NF-κBp65 might be a potential target for treating CIP, a neuropathic pain generated by tumor cell–induced injury to nerves that innervate the skin.
- Published
- 2015
4. Promoter demethylation of cystathionine-β-synthetase gene contributes to inflammatory pain in rats
- Author
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Fei-Hu Qi, Jin Tao, You-Lang Zhou, Guang-Yin Xu, Ying Xiao, Jianguo G. Gu, and Xinghong Jiang
- Subjects
biology ,Chemistry ,DNA damage ,Pharmacology ,Aminooxyacetic acid ,Cystathionine beta synthase ,chemistry.chemical_compound ,Anesthesiology and Pain Medicine ,DNA demethylation ,Neurology ,Biochemistry ,Hyperalgesia ,DNA methylation ,medicine ,biology.protein ,Neurology (clinical) ,Signal transduction ,medicine.symptom ,Protein kinase A - Abstract
Hydrogen sulfide (H2S), an endogenous gas molecule synthesized by cystathionine-β-synthetase (CBS), is involved in inflammation and nociceptive signaling. However, the molecular and epigenetic mechanisms of CBS-H2S signaling in peripheral nociceptive processing remain unknown. We demonstrated that peripheral inflammation induced by intraplantar injection of complete Freund adjuvant significantly up-regulated expression of CBS at both protein and mRNA levels in rat dorsal root ganglia (DRG). The CBS inhibitors hydroxylamine and aminooxyacetic acid attenuated mechanical hyperalgesia in a dose-dependent manner and reversed hyperexcitability of DRG neurons in inflamed rats. Intraplantar administration of NaHS (its addition mimics CBS production of H2S) or l -cysteine in healthy rats elicited mechanical hyperalgesia. Application of NaHS in vitro enhanced excitability and tetrodotoxin (TTX)-resistant sodium current of DRG neurons from healthy rats, which was attenuated by pretreatment of protein kinase A inhibitor H89. Methylation-specific PCR and bisulfite sequencing demonstrated that promoter region of cbs gene was less methylated in DRG samples from inflamed rats than that from controls. Peripheral inflammation did not alter expression of DNA methyltransferase 3a and 3b, the 2 major enzymes for DNA methylation, but led to a significant up-regulation of methyl-binding domain protein 4 and growth arrest and DNA damage inducible protein 45α, the enzymes involved in active DNA demethylation. Our findings suggest that epigenetic regulation of CBS expression may contribute to inflammatory hyperalgesia. H2S seems to increase TTX-resistant sodium channel current, which may be mediated by protein kinase A pathway, thus identifying a potential therapeutic target for the treatment of chronic pain.
- Published
- 2013
5. Enhanced binding capability of nuclear factor-κB with demethylated P2X3 receptor gene contributes to cancer pain in rats.
- Author
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You-Lang Zhou, Guo-Qin Jiang, Jinrong Wei, Hong-Hong Zhang, Wei Chen, Hongyan Zhu, Shufen Hu, Xinghong Jiang, Guang-Yin Xu, Zhou, You-Lang, Jiang, Guo-Qin, Wei, Jinrong, Zhang, Hong-Hong, Chen, Wei, Zhu, Hongyan, Hu, Shufen, Jiang, Xinghong, and Xu, Guang-Yin
- Published
- 2015
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