Results 11 to 20 of about 434,844 (347)

SYNTHESIS OF 1,3,4-OXADIAZOLES AS SELECTIVE T-TYPE CALCIUM CHANNEL INHIBITORS. [PDF]

open access: diamondHeterocycles, 2020
Zhang M   +10 more
europepmc   +2 more sources

Genetic deletion of Cav3.2 T-type calcium channels abolishes H2S-dependent somatic and visceral pain signaling in C57BL/6 mice

open access: goldJournal of Pharmacological Sciences, 2019
We tested whether genetic deletion of Cav3.2 T-type Ca2+ channels abolishes hydrogen sulfide (H2S)-mediated pain signals in mice. In Cav3.2-expressing HEK293 cells, Na2S, an H2S donor, at 100 μM clearly increased Ba2+ currents, as assessed by whole-cell ...
Kazuki Matsui   +13 more
doaj   +2 more sources

T-Type Calcium Channels: A Mixed Blessing

open access: yesInternational Journal of Molecular Sciences, 2022
The role of T-type calcium channels is well established in excitable cells, where they preside over action potential generation, automaticity, and firing. They also contribute to intracellular calcium signaling, cell cycle progression, and cell fate; and, in this sense, they emerge as key regulators also in non-excitable cells.
Dario Melgari   +5 more
openaire   +2 more sources

N-/T-Type vs. L-Type Calcium Channel Blocker in Treating Chronic Kidney Disease: A Systematic Review and Meta-Analysis

open access: yesPharmaceuticals, 2023
Renin-angiotensin system (RAS) inhibitors and calcium channel blockers (CCB) are often used together in chronic kidney disease (CKD). The PubMed, EMBASE, and Cochrane Library databases were searched to identify randomized controlled trials (RCTs) in ...
Mingming Zhao   +9 more
doaj   +1 more source

Structure, gating, and pharmacology of human CaV3.3 channel

open access: yesNature Communications, 2022
T-type calcium channels are implicated in many diseases. Here, multiple structures of CaV3.3 channel elucidate molecular mechanisms of T-type CaV channels activation at low voltage and interaction with different clinically used channel blockers.
Lingli He   +13 more
doaj   +1 more source

Verapamil Block of T-Type Calcium Channels [PDF]

open access: yesMolecular Pharmacology, 2011
Verapamil is a prototypical phenylalkylamine (PAA), and it was the first calcium channel blocker to be used clinically. It tonically blocks L-type channels in the inner pore with micromolar affinity, and its affinity increases at depolarized membrane potentials.
Pamela, Bergson   +4 more
openaire   +2 more sources

Inactivation of CACNA1H induces cell apoptosis by initiating endoplasmic reticulum stress in glioma

open access: yesTranslational Neuroscience, 2023
Ca2+ channels are abnormally expressed in various tumor cells and are involved in the progression of human glioma. Here, we explored the role of a calcium channel, voltage-dependent, T-type, alpha 1H subunit (CACNA1H), which encodes T-type Ca2+ channel ...
Liu Sheng   +3 more
doaj   +1 more source

T-type calcium channels in neuropathic pain [PDF]

open access: yesPain, 2016
Pain is a quite frequent complaint accompanying numerous pathologies. Among these pathological cases, numerous neuropathies are retrieved with identified etiologies (chemotherapies, diabetes, surgeries…) and also more diffuse syndromes such as fibromyalgia. More broadly, pain is one of the first consequences of most inherited diseases.
Bourinet, Emmanuel   +2 more
openaire   +3 more sources

Effect of Efonidipine on TGF-β1–Induced Cardiac Fibrosis Through Smad2-Dependent Pathway in Rat Cardiac Fibroblasts

open access: yesJournal of Pharmacological Sciences, 2011
.: Transforming growth factor beta-1 (TGF-β1) plays a critical role in progression of cardiac fibrosis, which may involve intracellular calcium change. We examined effects of efonidipine, a dual T-type and L-type calcium channel blocker (CCB), on TGF-β1 ...
Bai Lei   +10 more
doaj   +1 more source

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