Results 1 to 10 of about 5,036 (195)

Calcium Release from Stores Inhibits GIRK

open access: yesCell Reports, 2016
Synaptic transmission is mediated by ionotropic and metabotropic receptors that together regulate the rate and pattern of action potential firing. Metabotropic receptors can activate ion channels and modulate other receptors and channels.
Paul Kramer, John Williams
exaly   +6 more sources

Targeting GIRK Channels for the Development of New Therapeutic Agents [PDF]

open access: yesFrontiers in Pharmacology, 2011
G protein-coupled inward rectifier K+ (GIRK) channels represent novel targets for the development of new therapeutic agents. GIRK channels are activated by a large number of G protein-coupled receptors (GPCRs) and regulate the electrical activity of ...
Kenneth Walsh
exaly   +7 more sources

GIRK Channels as Candidate Targets for the Treatment of Substance Use Disorders

open access: yesBiomedicines, 2022
Substance use disorders (SUDs) are chronic, lifelong disorders that have serious consequences. Repeated substance use alters brain function. G-protein-activated inwardly rectifying potassium (GIRK) channels are expressed widely in the brain, including ...
Kazutaka Ikeda, Soichiro Ide
exaly   +4 more sources

Direct modulation of G protein-gated inwardly rectifying potassium (GIRK) channels [PDF]

open access: yesFrontiers in Physiology
Ion channels play a pivotal role in regulating cellular excitability and signal transduction processes. Among the various ion channels, G-protein-coupled inwardly rectifying potassium (GIRK) channels serve as key mediators of neurotransmission and ...
Paul Slesinger, Ian Glaaser
exaly   +4 more sources

Epilepsy in a mouse model of GNB1 encephalopathy arises from altered potassium (GIRK) channel signaling and is alleviated by a GIRK inhibitor

open access: yesFrontiers in Cellular Neuroscience, 2023
De novo mutations in GNB1, encoding the Gβ1 subunit of G proteins, cause a neurodevelopmental disorder with global developmental delay and epilepsy, GNB1 encephalopathy.
Nathan Dascal   +2 more
exaly   +5 more sources

Live-cell quantitative monitoring reveals distinct, high-affinity Gβγ regulations of GIRK2 and GIRK1/2 channels [PDF]

open access: yesNature Communications
Gi/o protein-coupled receptors (GPCRs) inhibit cardiac and neuronal excitability via G protein-activated K+ channels (GIRK), assembled by combinations of GIRK1 - GIRK4 subunits.
Reem Handklo-Jamal   +18 more
doaj   +3 more sources

GABAB receptor‐mediated modulation of sensory neuron excitability: Roles of CaV2.2, G‐protein‐coupled inwardly rectifying potassium (GIRK) channels, and hyperpolarisation‐activated cyclic nucleotide‐gated (HCN) channels in human and mouse nociception [PDF]

open access: yesExperimental Physiology
Chronic visceral pain is a key symptom of irritable bowel syndrome. Modulation of voltage‐gated calcium and potassium channels by G protein‐coupled receptors plays a key role in dampening nociceptive transmission.
Mariana Brizuela   +4 more
doaj   +2 more sources

Membrane-associated estrogen receptor α prevents the amyloid β-induced suppression of GIRK channel activity in hippocampal neurons from female mice [PDF]

open access: yesBiology of Sex Differences
Background Amyloid β oligomers (oAβ) are a key pathogenic driver in Alzheimer’s Disease (AD). Neuronal G protein-gated inwardly rectifying K+ (GIRK/Kir3) channels are important regulators of neuronal excitability and prominent somatodendritic effectors ...
Haichang Luo   +7 more
doaj   +2 more sources

Loss of expression and function of Gβγ by GNB1 encephalopathy-associated L95P mutation of the Gβ1 subunit [PDF]

open access: yesFrontiers in Pharmacology
BackgroundG-proteins areindispensable regulators of cellular signaling, with G-protein-gated inwardly rectifying potassium channels (GIRK) as key effectors. GNB1 encephalopathy (GNB1E) is a congenital neurological syndrome resulting from mutations in the
Haritha P. Reddy   +6 more
doaj   +2 more sources

Reactivating the phototransduction cascade with a mutation agnostic gene therapy preserves vision in rod-cone dystrophies [PDF]

open access: yesiScience
Summary: Rod-cone dystrophy (RCD) comprises genetic conditions where rod photoreceptor degeneration leads to cone loss, causing progressive vision loss.
Cardillia-Joe Simon   +18 more
doaj   +2 more sources

Home - About - Disclaimer - Privacy