https://nova.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 The relationship of exhaled nitric oxide to airway inflammation and responsiveness in children https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:532 Thu 25 Jul 2013 09:10:32 AEST ]]> Room temperature synthesis and binding studies of solution-processable histamine-imprinted microspheres https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:36741 Thu 02 Jul 2020 16:31:42 AEST ]]> Assessment of the binding performance of histamine-imprinted microspheres by frontal analysis capillary electrophoresis https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:31522 Kd ∼ 0.4 mM). FACE was easily carried out at shorter binding equilibration time (i.e. 30 min) and without the need to separate the microspheres, circumventing laborious and, in the case of the system under study, inefficient sample filtration. It also allowed for competitive binding studies by virtue of its ability to distinctly separate intact microspheres and all tested amines which could not be resolved in HPLC. Kd’s for nonimprinted (control) microspheres (NIM) from FACE and HPLC were also comparable (∼ 0.6 mM) but at higher histamine concentrations, HPLC gave lower histamine binding. This discrepancy was attributed to inefficient filtration of the batch binding samples prior to HPLC analysis resulting in an over-estimation of the concentration of free histamine brought about by the presence of unfiltered histamine-bound microspheres.]]> Sat 24 Mar 2018 08:43:51 AEDT ]]> Elevated serum cytokines during human anaphylaxis: identification of potential mediators of acute allergic reactions https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:7164 Sat 24 Mar 2018 08:34:16 AEDT ]]> Anaphylaxis: clinical patterns, mediator release, and severity https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:14482 Sat 24 Mar 2018 08:25:52 AEDT ]]> Extracellular Ca<sup>2+</sup> entry and mobilization of inositol trisphosphate-dependent Ca<sup>2+</sup> stores modulate histamine and electrical field stimulation induced contractions of the guinea-pig prostate https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:18122 2+ mobilization that leads to the contractile response to either exogenously added histamine (1 μM–1 mM) or electrical field stimulation (10 Hz, 0.5 ms, 60 V). Removal of extracellular Ca2+ by removal of Ca2+ from the bathing medium reduced histamine (1 mM) induced responses by 34% and responses induced by electrical field stimulation by 94%. Similarly, blockade of L-type Ca2+ channels by nifedipine (1 μM) reduced histamine (1 mM) induced responses by 43% and responses induced by electrical field stimulation by 77%. Application of cyclopiazonic acid (CPA) (10 μM) to inhibit Ca2+ reuptake to the sarcoplasmic reticulum enhanced both histamine-induced and electrical field stimulation induced responses to a small degree, while the addition of the inosotol triphosphate (IP3) receptor antagonist, 2-aminophenoxyethane borane (2-APB) (100 μM) inhibited histamine induced responses by 70% and electrical field stimulation induced responses by 57%. Ryanodine (1 μM) did not affect contractile responses to either histamine or electrical field stimulation, either in the absence or presence of 2-APB (100 μM). During both histamine and electrical field stimulation induced contractions, prostate smooth muscle generates IP3 receptor mediated Ca2+ release in conjunction with Ca2+ entry from the extracellular environment. Ryanodine receptors on the other hand, appear not to play a role in this physiological mechanism.]]> Sat 24 Mar 2018 08:04:47 AEDT ]]> Ions, channels, and receptors https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:3157 Sat 24 Mar 2018 07:18:08 AEDT ]]>