WordNet

existing in possibility; "a potential problem"; "possible uses of nuclear power" (同)possible
the inherent capacity for coming into being (同)potentiality, potency
a cellular structure that is postulated to exist in order to mediate between a chemical agent that acts on nervous tissue and the physiological response

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1. 血管新生阻害剤の概要 overview of angiogenesis inhibitors
2. 心筋活動電位および抗不整脈剤の作用 myocardial action potential and action of antiarrhythmic drugs
3. インスリン受容体の構造および機能 structure and function of the insulin receptor
4. T細胞受容体シグナル伝達 t cell receptor signaling
5. アンギオテンシン変換酵素阻害剤とアンギオテンシン受容体拮抗剤との相違 differences between angiotensin converting enzyme inhibitors and receptor blockers

Craighead DH1, Alexander LM2.
Microvascular research.Microvasc Res.2016 Apr 27;107:39-45. doi: 10.1016/j.mvr.2016.04.010. [Epub ahead of print]
Menthol, the active ingredient in several topically applied analgesics, activates transient receptor potential melastatin 8 (TRPM8) receptors on sensory nerves and on the vasculature inducing a cooling sensation on the skin. Ilex paraguariensis is also a common ingredient in topical analgesics that
PMID 27131832

Hydrogen sulfide depolarizes neurons in the nucleus of the solitary tract of the rat.

Malik R1, Ferguson AV2.
Brain research.Brain Res.2016 Feb 15;1633:1-9. doi: 10.1016/j.brainres.2015.12.029. Epub 2015 Dec 23.
Hydrogen sulfide (H2S) is a gasotransmitter that has been described to affect the membrane potential of neurons in a number of brain areas. Using whole cell patch-clamp electrophysiological techniques, we investigated the effects of H2S on the membrane potential of neurons in the nucleus of the soli
PMID 26721687

Dunn WR1, Alexander SP2, Ralevic V2, Roberts RE2.
Pharmacology & therapeutics.Pharmacol Ther.2016 Feb;158:101-13. doi: 10.1016/j.pharmthera.2015.12.007. Epub 2015 Dec 17.
In recent years, it has become apparent that the gaseous pollutant, hydrogen sulphide (H2S) can be synthesised in the body and has a multitude of biological actions. This review summarizes some of the actions of this 'gasotransmitter' in influencing the smooth muscle that is responsible for controll
PMID 26706238

Enhancing Effects of Salicylate on Quinidine-Induced Block of Human Wild Type and LQT3 Related Mutant Cardiac Na+ Channels

Urashima Tadashi,Hisatome Ichiro,Mizuta Einosuke,Miake Junichiro,Adachi Masamitsu,Ogura Kazuyoshi,Kato Masaru,Yano Akio,Kato Masahiko
Journal of Arrhythmia 27(Supplement), OP04_3, 2011
… Salicylate enhanced the quinidine-induced tonic block and UDB of both wild-type hH1 and hSkM1 currents at a holding potential (HP) of −100 mV but not at a HP of −140 mV. … Salicylate further produced a shift of the steady-state inactivation curve of hH1 toward hyperpolarizing direction in the presence of quinidine. … Based on the modulated receptor theory, it is probable that salicylate decreases the dissociation constant for quinidine binding to inactivated state channels. …
NAID 130002130439

宮崎俊一,MIYAZAKI Shunichi
東京女子医科大学雑誌 78(1), 61-68, 2008-01
… These properties were implicated in the electrical polyspermy block due to overshoot of the fertilization potential. … In 1981, we recorded long-lasting repetitive hyperpolarizing responses during fertilization of hamster eggs. … In 1992, we showed that each Ca2+ rise is due to Ca2+ release from the endoplasmic reticulum through inositol 1, 4, 5-trisphosphate receptor (IP_3R), forming a Ca2+ wave based on Ca2+ -induced Ca2+ release. …
NAID 110007524599

三好博史
Journal of smooth muscle research. Japanese section 8(2), "J-77"-"J-88", 2004-08-28
… The membrane potential is regulated by various types of ion channels. … K^+ channels play important roles in controlling the resting potential and repolarization of action potentials. … Both channels regulate the resting potential to keep the myometrium quiescent and are suggested to be a target of β-stimulants. … Transient receptor potential channels have been identified in human myometrium and PHM1-41 cells using RT-PCR. …
NAID 110002694898