Haiqiang Dou

ORCID: 0000-0002-1551-4114
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Pancreatic function and diabetes
  • Receptor Mechanisms and Signaling
  • Diabetes Management and Research
  • Neuroscience and Neuropharmacology Research
  • Photoreceptor and optogenetics research
  • Diabetes and associated disorders
  • Neurotransmitter Receptor Influence on Behavior
  • Ion channel regulation and function
  • Diabetes Treatment and Management
  • Cellular transport and secretion
  • Toxic Organic Pollutants Impact
  • Nicotinic Acetylcholine Receptors Study
  • Pluripotent Stem Cells Research
  • Erythrocyte Function and Pathophysiology
  • Blood properties and coagulation
  • Pancreatitis Pathology and Treatment
  • Lipid Membrane Structure and Behavior
  • Diet, Metabolism, and Disease
  • Air Quality and Health Impacts
  • Neuroscience and Neural Engineering
  • Cannabis and Cannabinoid Research
  • Dam Engineering and Safety
  • Geotechnical Engineering and Underground Structures
  • Calcium signaling and nucleotide metabolism
  • Endoplasmic Reticulum Stress and Disease

University of Gothenburg
2018-2025

Peking University
2006-2020

McGovern Institute for Brain Research
2014-2015

Center for Life Sciences
2011-2015

Institute of Molecular Medicine
2015

Laboratoire de Biologie Physico-Chimique des Protéines Membranaires
2015

Chinese Institute for Brain Research
2014

First Automotive Works (China)
2013

Gansu Agricultural University
2009

University of Tsukuba
2001

Glucagon is the body's main hyperglycemic hormone, and its secretion dysregulated in type 2 diabetes mellitus (T2DM). The incretin hormone glucagon-like peptide-1 (GLP-1) released from gut used T2DM therapy. Uniquely, it both stimulates insulin inhibits glucagon thereby lowers plasma glucose levels. In this study, we have investigated action of GLP-1 on release human pancreatic islets. Immunocytochemistry revealed that only <0.5% α-cells possess detectable GLP-1R immunoreactivity. Despite...

10.14814/phy2.13852 article EN cc-by Physiological Reports 2018-09-01

By restoring glucose-regulated insulin secretion, glucagon-like peptide-1–based (GLP-1–based) therapies are becoming increasingly important in diabetes care. Normally, the incretins GLP-1 and glucose-dependent insulinotropic polypeptide (GIP) jointly maintain normal blood glucose levels by stimulation of secretion pancreatic β cells. However, reason why only GLP-1–based drugs effective improving after presentation has not been resolved. ATP-sensitive K+ (KATP) channels play a crucial role...

10.1172/jci140046 article EN Journal of Clinical Investigation 2020-11-15

Glucose-induced insulin secretion depends on β-cell electrical activity. Inhibition of ATP-regulated potassium (KATP) channels is a key event in this process. However, KATP channel closure alone not sufficient to induce activity; activation depolarizing membrane current also required. Here we examine the role mechanosensor ion PIEZO1 Yoda1, specific agonist, activates small and thereby triggers activity with resultant stimulation Ca2+-influx secretion. Conversely, antagonist GsMTx4 reduces...

10.1038/s41467-022-31103-y article EN cc-by Nature Communications 2022-07-22

Abstract The generation of pancreatic cell types from renewable sources holds promise for replacement therapies diabetes. Although most effort has focused on generating beta cells, considerable evidence indicates that glucagon secreting alpha cells are critically involved in disease progression and proper glucose control. Here we report the stem cell-derived human (SC-alpha) pluripotent via a transient pre-alpha intermediate. These exhibit transcriptional profile similar to mature although...

10.1038/s41467-020-16049-3 article EN cc-by Nature Communications 2020-05-07

Whole-body glucose homeostasis is coordinated through secretion of glucagon and insulin from pancreatic islets. When low, released α-cells to stimulate hepatic production. However, the mechanisms that regulate remain unclear. Here we show in α-cells, interaction between fatty acid oxidation metabolism controls secretion. The glucose-dependent inhibition relies on pyruvate dehydrogenase carnitine palmitoyl transferase 1a activity lowering mitochondrial by increases glucose. This results...

10.2337/db23-0056 article EN Diabetes 2023-07-26

Significance With a combination of HPLC and carbon fiber electrodes, we demonstrate that grafted neural stem cells directly release dopamine in the damaged striatum vivo partially rescue Parkinson’s disease (PD) model. ( i ) Primitive cell–dopamine-like neuron (pNSC–DAn) retained tyrosine hydroxylase expression reduced PD-like asymmetric rotation; ii depolarization-evoked reuptake were significantly rescued vitro (brain slices) vivo, as determined jointly by microdialysis-based...

10.1073/pnas.1408484111 article EN Proceedings of the National Academy of Sciences 2014-10-20

Key points The timing of synaptic transmission is critical to plasticity in the striatum. However, striatal dopamine (DA) release induced by cholinergic interneurons (ChIs) striatum unclear. In this study, we focused on temporal components DA and replenishment triggered different pathways. We show that stimulation ChIs induces with a total delay 20.6 ms, including 2.8 ms for action potential firing ChIs, 7.0 between acetylcholine terminals terminals, 10.8 downstream release. via ChI pathway...

10.1113/jphysiol.2014.271825 article EN The Journal of Physiology 2014-06-28

Abstract Recent work has shown that chemical release during the fundamental cellular process of exocytosis in model cell lines is not all‐or‐none. We tested this theory for vesicular from single pancreatic beta cells. The vesicles these cells insulin, but also serotonin, which detectible with amperometric methods. Traditionally, it assumed Here, we use a multidisciplinary approach involving nanoscale methods to explore nature insulin exocytosis. amperometrically quantified number serotonin...

10.1002/anie.202015902 article EN Angewandte Chemie International Edition 2020-12-19

The pancreatic islet hormones insulin, glucagon and somatostatin play a crucial role in maintaining normoglycaemia. Effective communication between beta, alpha, delta cells is essential for glucose homeostasis disruption of this intra-islet crosstalk observed diabetes. Optogenetics great way to study islets as it eliminates the need drugs that might have off-target effects, while preserving architecture. We generated mouse models optogenetics interrogate physiological humoral response...

10.1101/2025.03.18.643880 preprint EN cc-by-nc bioRxiv (Cold Spring Harbor Laboratory) 2025-03-19

By stimulating hepatic glucose production, glucagon (released by islet α-cells) restores normal blood levels when they fall below the range. We used optogenetics in conjunction with electrophysiology, [Ca2+]i imaging and hormone release measurements to explore intrinsic paracrine regulation of secretion. Many α-cells were spontaneously active at 1mM glucose. However, up ∼50% α- cells electrically silent. KATP channel blockade, amino acids somatostatin receptor (SSTR) antagonism restored...

10.2337/db24-1053 article EN Diabetes 2025-04-04

&lt;p dir="ltr"&gt;&lt;b&gt;By stimulating hepatic glucose production, glucagon (released by islet α-cells) restores normal blood levels when they fall below the range. We &lt;/b&gt;&lt;b&gt;used&lt;/b&gt;&lt;b&gt; optogenetics in conjunction with electrophysiology, [Ca&lt;/b&gt;&lt;sup&gt;&lt;strong&gt;2+&lt;/strong&gt;&lt;/sup&gt;&lt;b&gt;]&lt;/b&gt;&lt;sub&gt;&lt;strong&gt;i&lt;/strong&gt;&lt;/sub&gt;&lt;b&gt; imaging and hormone release measurements to explore intrinsic paracrine...

10.2337/figshare.28715987.v1 preprint EN 2025-04-04

&lt;p dir="ltr"&gt;&lt;b&gt;By stimulating hepatic glucose production, glucagon (released by islet α-cells) restores normal blood levels when they fall below the range. We &lt;/b&gt;&lt;b&gt;used&lt;/b&gt;&lt;b&gt; optogenetics in conjunction with electrophysiology, [Ca&lt;/b&gt;&lt;sup&gt;&lt;strong&gt;2+&lt;/strong&gt;&lt;/sup&gt;&lt;b&gt;]&lt;/b&gt;&lt;sub&gt;&lt;strong&gt;i&lt;/strong&gt;&lt;/sub&gt;&lt;b&gt; imaging and hormone release measurements to explore intrinsic paracrine...

10.2337/figshare.28715987 preprint EN 2025-04-04

10.1007/s12239-013-0058-3 article EN International Journal of Automotive Technology 2013-07-27

Action potential (AP) patterns and dopamine (DA) release are known to correlate with rewarding behaviors, but how codes of AP bursts translate into DA in vivo remains elusive. Here, a given pattern was defined by four codes, termed total number, frequency, number bursts, interburst time [N, f, b, i].. The 'burst effect' calculated the ratio (γ) overflow multiple that single burst when fixed. By stimulating medial forebrain bundle using at either physiological (20 Hz) or supraphysiological...

10.1111/j.1471-4159.2011.07440.x article EN Journal of Neurochemistry 2011-08-20

Abstract Recent work has shown that chemical release during the fundamental cellular process of exocytosis in model cell lines is not all‐or‐none. We tested this theory for vesicular from single pancreatic beta cells. The vesicles these cells insulin, but also serotonin, which detectible with amperometric methods. Traditionally, it assumed Here, we use a multidisciplinary approach involving nanoscale methods to explore nature insulin exocytosis. amperometrically quantified number serotonin...

10.1002/ange.202015902 article EN Angewandte Chemie 2020-12-19

While glucose-stimulated insulin secretion depends on Ca(2+) influx through voltage-gated channels in the cell membrane of pancreatic β-cell, there is also ample evidence for an important role intracellular stores secretion, particularly relation to drug stimuli. We report here that thiopental, a common anesthetic agent, triggers from intact pancreas and primary cultured rat β-cells. investigated underlying mechanisms by measurements whole K(+) currents, potential, cytoplasmic concentration...

10.1152/ajpcell.00081.2011 article EN AJP Cell Physiology 2011-12-02
Coming Soon ...