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- ...muscarinic [[acetylcholine receptor]]s ([[acetylcholine]] being the main [[neurotransmitter]] used by the [[parasympathetic]] nervous system). Therefore, it may cause ...upillary sphincter]] muscle, which is normally stimulated by acetylcholine release, thereby allowing the radial [[pupillary dilator]] [[muscle]] to contract a16 KB (2,198 words) - 16:46, 27 September 2010
- ...f needed to assess potential adverse effects on patients.<ref>{{cite press release |title=Severe Pain Relief may be Possible with a Common Anesthetic Drug |pu .... NMDA and AMPA are receptors for the [[neurotransmitter]] [[Glutamic acid#Neurotransmitter|glutamate]]. The glutamate system has been implicated in depression recentl69 KB (9,697 words) - 21:01, 24 September 2010
- ...he muscarinic [[acetylcholine receptor]]s ([[Acetylcholine]] is the main [[neurotransmitter]] used by the [[parasympathetic]] nervous system). Therefore, it may cause ...upillary sphincter]] muscle, which is normally stimulated by acetylcholine release, thereby allowing the radial [[pupillary dilator]] [[muscle]] to contract a15 KB (1,975 words) - 15:07, 6 July 2010
- Valproate is believed to affect the function of the [[neurotransmitter]] [[GABA]] in the human brain, making it an alternative to [[Lithium pharma | title = FDA Issues Approvable Letter For Stavzor Delayed Release Valproic Acid Capsules25 KB (3,328 words) - 16:47, 27 September 2010
- ...by the [[hypothalamus]]. Its main function as a hormone is to inhibit the release of [[prolactin]] from the anterior lobe of the [[pituitary]]. ...[[norepinephrine]] (noradrenaline) and [[epinephrine]] (adrenaline), but a neurotransmitter as well.48 KB (6,470 words) - 16:48, 27 September 2010
- '''Epinephrine''' (also known as '''adrenaline''') is a [[hormone]] and [[neurotransmitter]].<ref>{{cite pmid|6278965}}</ref>. It increases heart rate, contracts bloo ...aline from the cytosol back into chromaffin granules in preparation for release.{{Citation needed|date=April 2009}}22 KB (2,916 words) - 16:50, 27 September 2010
- ...}}</ref> The pharmacological action of diazepam enhances the effect of the neurotransmitter GABA by binding to the benzodiazepine site on the [[GABAA receptor|GABA<sub ** Capsules, time-release – 15 mg (marketed by Roche as '''Valrelease''')<ref name="ElephantCa78 KB (10,295 words) - 16:51, 27 September 2010
- ...ain pharmacological action of temazepam is to increase the effect of the [[neurotransmitter]] [[GABA]] (gamma-aminobutyric acid) at the GABA<sub>A</sub> receptor. This ...or=Welt T, Engelmann M, Renner U, ''et al.'' |title=Temazepam triggers the release of vasopressin into the rat hypothalamic paraventricular nucleus: novel ins45 KB (6,129 words) - 22:16, 19 September 2010
- Natural release of the hormone [[oxytocin]] can cause mild to moderate mydriasis. Strong se ...sed for this task however. Any potent norepinephrine reuptake inhibitor or release agent should be capable of such an effect.9 KB (1,223 words) - 09:40, 20 September 2010
- ...{{cite journal |author=Korenke AR, Rivey MP, Allington DR |title=Sustained-release fampridine for symptomatic treatment of multiple sclerosis |journal=Ann Pha ..., prolonging [[action potentials]] and thereby increasing neurotransmitter release at the [[neuromuscular junction]].<ref>{{cite journal |author=Judge S, Beve9 KB (1,146 words) - 09:44, 20 September 2010
- ...A receptors does not occur. The administration of sulbutiamine reduces the release of [[dopamine]] in the prefrontal cortex, which increases the density of D<19 KB (2,584 words) - 13:11, 20 September 2010
- ...he salivary glands of the [[octopus]] and has since been found to act as [[neurotransmitter]], [[neurohormone]] and [[neuromodulator]] in [[invertebrate]]s. It is wide ...ne has a major role in learning and memory. In the [[firefly]], octopamine release leads to light production in the lantern.7 KB (980 words) - 13:14, 20 September 2010
- ...ut bullets lodged in the joints are the exception, as they deteriorate and release lead into the body over time.<ref>{{cite pmid|2926538}}</ref> ...ure takes place over years, clearance is much slower, partly due to the re-release of lead from bone.<ref name="Hu07"/> Many other tissues store lead, but tho90 KB (13,109 words) - 21:36, 20 September 2010
- ...h, in turn are derived from [[neuroectoderm]]. They release a variety of [[neurotransmitter]]s, including [[acetylcholine]], [[adenosine triphosphate|ATP]], and [[dopa ...2+</sup> entry, excitation of glomus cells and consequent neurotransmitter release <ref name="pmid10811732>{{cite journal |author=Buckler KJ, Williams BA, Hon10 KB (1,411 words) - 21:27, 21 September 2010
- ...]], the parasympathetic nervous system stimulates neurons that release the neurotransmitter [[acetylcholine]] (ACh) at synapses with [[cardiomyocyte|cardiac muscle cel3 KB (424 words) - 21:28, 21 September 2010
- ...e]]s (e.g. [[Antidiuretic hormone|vasopressin]] and [[angiotensin]]) and [[neurotransmitter]]s (e.g. [[epinephrine]]) from the nervous system. Permeability of the [[endothelium]] is pivotal in the release of nutrients to the tissue. It is also increased in [[inflammation]] in res8 KB (1,132 words) - 21:29, 21 September 2010
- ...rocannabinol (Δ<sup>8</sup>-THC), mimic the action of [[anandamide]], a [[neurotransmitter]] produced naturally in the body. The THCs produce the ''high'' associated ...cellular signaling role they are similar to the well-known [[monoamine]] [[neurotransmitter]]s, such as [[acetylcholine]] and [[dopamine]], endocannabinoids differ in49 KB (6,487 words) - 22:06, 21 September 2010
- ...tin was initially synthesized to mimic the [[chemical structure]] of the [[neurotransmitter]] gamma-aminobutyric acid ('''GABA'''), but is not believed to act on the s {{News release section|date=March 2010}}30 KB (4,025 words) - 22:06, 21 September 2010
- ...at: [http://books.google.com/books?id=nNH3p29wjK4C&pg=PA116&dq=endorphins+neurotransmitter&hl=en&ei=IwwlTKfzHMr-_Aa-w6zGBA&sa=X&oi=book_result&ct=result&resnum=10&ved ...By hijacking this process, exogenous opioids cause inappropriate dopamine release, and lead to aberrant [[synaptic plasticity]], which causes addiction. Opio18 KB (2,467 words) - 22:06, 21 September 2010
- ...synthesize and degrade the endocannabinoids anandamide and 2-AG. Unlike [[neurotransmitter]]s, endogenous cannabinoids are not stored in [[vesicle]]s after synthesis, ...ignaling in a variety of physiological processes, including neuromodulator release,<ref>{{cite journal |author=Fortin DA, Levine ES |title=Differential effect23 KB (3,059 words) - 22:08, 21 September 2010