ArticleNaunyn-Schmiedeberg's archives of pharmacology1994
P2-purinoceptor-mediated autoinhibition of sympathetic transmitter release in mouse and rat vas deferens.
Article in Naunyn-Schmiedeberg's archives of pharmacology, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
19 citing papers in PubMed, 49 citations in OpenAlex.
- P2Y Receptors in Synaptic Transmission and Plasticity: Therapeutic Potential in Cognitive Dysfunction.Neural plasticity · 2016Review
- Neuroeffector Ca2+ transients for the direct measurement of purine release and indirect measurement of cotransmitters in rodents.Experimental physiology · 2009Article
- P2 receptor-mediated modulation of neurotransmitter release-an update.Purinergic signalling · 2007Article
- P2Y purinoceptors inhibit exocytosis in adrenal chromaffin cells via modulation of voltage-operated calcium channels.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2000Article
- Individual sympathetic varicosities possess different sensitivities to alpha 2 and P2 receptor agonists and antagonists in mouse vas deferens.British journal of pharmacology · 1999Article
- ATP stimulates sympathetic transmitter release via presynaptic P2X purinoceptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1999Article
- Presynaptic modulation by L-glutamate and GABA of sympathetic co-transmission in rat isolated vas deferens.British journal of pharmacology · 1996Article
- Purinoceptor modulation of noradrenaline release in rat tail artery: tonic modulation mediated by inhibitory P2Y- and facilitatory A2A-purinoceptors.British journal of pharmacology · 1996Article
- Caffeine enhances sympathetic purinergic and noradrenergic transmission in the guinea-pig isolated vas deferens.Naunyn-Schmiedeberg's archives of pharmacology · 1995Article
- Cultured chick sympathetic neurons: modulation of electrically evoked noradrenaline release by P2-purinoceptors.Naunyn-Schmiedeberg's archives of pharmacology · 1995Article
- P2-purinoceptor-mediated inhibition of noradrenaline release in rat atria.British journal of pharmacology · 1995Article
- Effects of suramin on contractions of the guinea-pig vas deferens induced by analogues of adenosine 5'-triphosphate.British journal of pharmacology · 1995Article
- Noradrenaline release from rat sympathetic neurons evoked by P2-purinoceptor activation.Naunyn-Schmiedeberg's archives of pharmacology · 1994Article
- Evidence for P2-purinoceptor-mediated inhibition of noradrenaline release in rat brain cortex.British journal of pharmacology · 1994Article
- Blockade of P2X-purinoceptors by trypan blue in rat vas deferens.British journal of pharmacology · 1994Article
- Corelease of noradrenaline and ATP by brief pulse trains in guinea-pig vas deferens.Naunyn-Schmiedeberg's archives of pharmacology · 1994Article
- P1-purinoceptor-mediated modulation of neural noradrenaline and ATP release in guinea-pig vas deferens.Naunyn-Schmiedeberg's archives of pharmacology · 1994Article
- Blockade by 4,4'-diisothiocyanatostilbene-2,2'-disulphonate (DIDS) of P2X-purinoceptors in rat vas deferens.British journal of pharmacology · 1994Article
- Purinergic Receptors of the Central Nervous System: Biology, PET Ligands, and Their Applications.Molecular imagingReview
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Effects of drugs acting at P2-purinoceptors on the release of newly taken up [3H]-noradrenaline were studied in slices of mouse and rat vas deferens. The slices were superfused and stimulated electrically, in most experiments by trains of 60 pulses/8 Hz. In mouse vas deferens, the P2-purinoceptor antagonists reactive blue 2 (1.8-100 microM) and brilliant blue G (10-300 microM) increased the stimulation-evoked overflow of tritium in a concentration-dependent manner as shown previously for suramin. Reactive blue 2, which preferentially blocks the P2Y-subtype, was the most potent compound and the compound with highest maximal effect, an increase by 104%. Pyridoxal phosphate-6-azophenyl-2',4'-disulfonic acid (PPADS), in contrast, caused a small increase only at a single concentration (30 microM). The effects of reactive blue 2, brilliant blue G and suramin were not additive. The P2 agonist adenosine 5'-O-(3-thio)-triphosphate (ATP gamma S) reduced the evoked overflow of tritium. As shown previously for suramin, reactive blue 2 30 microM and brilliant blue G 100 microM antagonized the effect of ATP gamma S. From the shift of the ATP gamma S concentration-response curve to the right, an apparent pKB value of 5.3 was estimated for reactive blue 2 and an apparent pKB of 4.5 for brilliant blue G. In rat vas deferens, reactive blue 2 (3-30 microM), brilliant blue G (10 microM) and suramin (30-300 microM) also increased the evoked overflow of tritium. As in the mouse, reactive blue 2 was the most potent compound and the compound with highest maximal effect, an increase by 90%.(ABSTRACT TRUNCATED AT 250 WORDS)
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.