Hong Jiang

ORCID: 0000-0003-1524-7519
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Research Areas
  • Parkinson's Disease Mechanisms and Treatments
  • Trace Elements in Health
  • Glass properties and applications
  • Nuclear Receptors and Signaling
  • Iron Metabolism and Disorders
  • Regulation of Appetite and Obesity
  • Neurological diseases and metabolism
  • Biochemical Analysis and Sensing Techniques
  • Advancements in Battery Materials
  • Alzheimer's disease research and treatments
  • Crystallization and Solubility Studies
  • Neuroscience and Neuropharmacology Research
  • X-ray Diffraction in Crystallography
  • RNA regulation and disease
  • Nerve injury and regeneration
  • Transition Metal Oxide Nanomaterials
  • Adipose Tissue and Metabolism
  • Advanced Battery Materials and Technologies
  • Heavy Metal Exposure and Toxicity
  • Boron and Carbon Nanomaterials Research
  • Recycling and utilization of industrial and municipal waste in materials production
  • Hemoglobinopathies and Related Disorders
  • Neurological disorders and treatments
  • MXene and MAX Phase Materials
  • Surface Modification and Superhydrophobicity

Qingdao University
2016-2025

Affiliated Hospital of Qingdao University
2002-2025

Wuhan University
2008-2025

Renmin Hospital of Wuhan University
2008-2025

Hainan University
2014-2024

Qingdao Municipal Hospital
2024

Cosmetic (Greece)
2024

Yantai University
2014-2023

Fujian Medical University
2023

Hainan Agricultural School
2023

Our objective is to determine the neuromodulatory role of ghrelin in brain. To identify neurons that express receptor [GH secretagogue (GHS-R)], we generated GHS-R-IRES-tauGFP mice by gene targeting. Neurons expressing GHS-R exhibit green fluorescence and are clearly evident hypothalamus, hippocampus, cortex, midbrain. Using immunohistochemistry combination with fluorescent protein fluorescence, identified coexpress dopamine subtype 1 (D1R) GHS-R. The potential physiological relevance...

10.1210/me.2005-0084 article EN Molecular Endocrinology 2006-04-07

The gut-derived orexigenic peptide hormone ghrelin enhances neuronal firing in the substantia nigra pars compacta, where dopaminergic neurons modulate function of nigrostriatal system for motor coordination. Here we describe a novel mechanism by which nigral inhibiting voltage-gated potassium Kv7/KCNQ/M-channels through its receptor GHS-R1a and activation PLC-PKC pathway. Brain slice recordings compacta reveal that inhibits native Kv7/KCNQ/M-currents. This effect is abolished selective...

10.1038/ncomms2439 article EN cc-by-nc-sa Nature Communications 2013-02-05

Abstract We recently reported that expression levels of tumor necrosis factor (TNF) receptors, TNFR1 and TNFR2, are significantly changed in the brains cerebrospinal fluid (CSF) with Alzheimer's disease (AD). Moreover, we also found that, an mouse model, genetic deletion TNF receptor (TNFR1) reduces amyloid plaques beta peptides (Aβ) production through β-secretase (BACE1) regulation. TNF-α converting enzyme (TACE/ADAM-17) does not only cleave pro- but however, whether TACE activity was CSF...

10.1186/1750-1326-6-69 article EN cc-by Molecular Neurodegeneration 2011-10-06

Both ghrelin and somatostatin (SST) inhibit glucose-stimulated insulin secretion (GSIS) from pancreatic β-cells, but how these independent actions are regulated has been unclear. The mechanism must accommodate noncanonical receptor (GHS-R1a)-G-protein coupling to Gα(i/o) instead of Gα(q11) dependence on energy balance. Here we present evidence for an equilibrium model heteromerization that fulfills criteria. We show GHS-R1a rather than requires interactions between SST subtype 5 (SST5) in...

10.1073/pnas.1209590109 article EN Proceedings of the National Academy of Sciences 2012-10-29

Coke-resistant defect-confined Ni-based nanosheet-like catalysts derived from halloysites were developed for CO<sub>2</sub> reforming of methane.

10.1039/c8nr02006j article EN Nanoscale 2018-01-01
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