نتایج جستجو برای: muscarinic antagonists

تعداد نتایج: 58413  

Journal: :Investigative ophthalmology & visual science 1990
R J Walkenbach G S Ye

Particulate fractions from fresh bovine corneal endothelium exhibited high affinity, specific binding by a potent muscarinic cholinergic radioligand, [3H]QNB. Particulate fraction binding sites exhibited half maximal binding at approximately 0.3 nM [3H]QNB and reached a maximal binding capacity of 820 fmoles/mg of protein at 3 nM [3H]QNB. Muscarinic cholinergic antagonists and agonists competed...

Journal: :Investigative ophthalmology & visual science 1994
S Matsumoto T Yorio L DeSantis I H Pang

PURPOSE To characterize the pharmacology of the carbachol-induced changes of phospholipase C (PLC) activity and intracellular calcium concentration ([Ca2+]i) in cultured human ciliary muscle cells. METHODS Changes in PLC activity of cultured human ciliary muscle cells were determined by production of inositol phosphates. Single-cell dynamic fluorescence ratio imaging was used to determine [Ca...

Journal: :American journal of respiratory cell and molecular biology 2003
Reinoud Gosens S Adriaan Nelemans Mechteld M Grootte Bromhaar Sue McKay Johan Zaagsma Herman Meurs

Muscarinic receptor agonists have been considered to act synergistically in combination with growth facors on airway smooth muscle growth. Characterization of the proliferative responses and of the receptor subtype(s) involved has not yet been studied. Therefore, we investigated mitogenesis induced by stimulation of muscarinic receptors, alone and in combination with stimulation by platelet-der...

Journal: :American journal of physiology. Cell physiology 2000
M C Cilluffo E Esqueda N A Farahbakhsh

We have examined the interaction between muscarinic and alpha(2)-adrenergic receptor activation on inositol phosphate (IP) formation in the nonpigmented cells of the ciliary body epithelium (NPE cells) of the rabbit. We have compared these changes with those previously observed in the intracellular free Ca(2+) concentration. Whereas muscarinic receptor activation causes an increase in intracell...

Journal: :Journal of chemical neuroanatomy 2005
Fuencisla Pilar-Cuéllar Miguel Angel Paniagua Ricardo Mostany Carlos César Pérez Arsenio Fernández-López

In this work, we studied the in vitro G-protein activation induced by muscarinic agonists using [(35)S]guanylyl-5'-O-(gamma-thio)-triphosphate ([(35)S]GTPgammaS) autoradiographic methods to characterize the M(2) and M(4) muscarinic subtypes response. Thus, we describe a detailed characterization of the increases in [(35)S]GTPgammaS binding elicited by carbachol (Cch) and oxotremorine (OXO) (bin...

Journal: :Bioscience trends 2010
Ryo Orii Yasuhiko Sugawara Shigehito Sawamura Yoshitsugu Yamada

Information about the muscarinic receptor subtype(s) mediating pulmonary circulatory vasodilator responses to acetylcholine (ACh) is limited. The aim of this study was to pharmacologically characterize the muscarinic receptors associated with ACh-induced pulmonary vasodilation in a pulmonary hypertension model. Vasodilation of rabbit isolated buffer-perfused lungs in which pulmonary hypertensio...

Journal: :Brain research bulletin 2008
Behnaz Esmaeili Zahra Basseda Ahmad Reza Dehpour

M1 muscarinic receptor has been shown to be involved in cognitive functions of the brain. Conditioned place preference (CPP) paradigm involves memory for the association between environmental stimuli and the rewarding properties produced by a treatment. Using a balanced CPP design, we studied the possible involvement of M1 muscarinic receptors on the acquisition, expression and consolidation of...

Journal: :Chemical & pharmaceutical bulletin 2000
G R Mandelli S Maiorana P Terni G Lamperti M L Colibretti B P Imbimbo

A series of 5H-dibenz[b,f]azepine derivatives was prepared and evaluated for binding affinities to muscarinic receptors in vitro. Among them, compound 8 showed a high affinity for human recombinant M2 receptors (Ki=2.6 nm), a low affinity for M4 receptors (39-fold less than for M2 receptors) and a very low affinity for M1 and M3 receptors (119- and 112-fold less than for M2 receptors, respectiv...

2017
Nana Du Yanfang Liu Xiuli Zhang Jixia Wang Jianqiang Zhao Jian He Han Zhou Lijuan Mei Xinmiao Liang

Scopolia tangutica (S. tangutica) is a traditional Chinese medicinal plant used for antispasmodics, anesthesia, analgesia and sedation. Its pharmacological activities are mostly associated with the antagonistic activity at muscarinic acetylcholine receptors (mAchRs) of several known alkaloids such as atropine and scopolamine. With our recent identification of four hydroxycinnamic acid amides fr...

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