4,288 research outputs found

    Role of atrial receptors in the control of sodium excretion

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    Responses of an innervated and a contralateral chronically denervated kidney to mild positive pressure breathing are compared for saline volume expansions in chloralose anesthetized dogs. It is shown that mild pressure breathing significantly reduces sodium excretion, urine flow, free water clearance, and PAH clearance. After 20 minutes of positive pressure breathing, both kidney responses are identical suggesting the release of natriuretic hormone which reduces renal function in addition to the demonstrated change in renal nerve activity. Increase of the left atrial pressure through balloon obstruction of the mitral orifice increases urine flow, sodium excretion and PAH clearance; inflation of the balloon and positive pressure breathing again depresses renal function. Preliminary evidence indicates that receptors in the right atrium are more severely affected by pressure breathing than those in the left atrium

    Monitoring cardiovascular function in the primate under prolonged weightlessness

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    Monitoring cardiovascular function in primates under prolonged weightlessnes

    The impact of a changing financial climate on a UK local charitable sector: voices from the front line

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    Forced to compete with private and public sector providers, charities experience tensions as the quest for a more commercially-oriented position may conflict with their social imperative. Little attention has been given to understanding the experiences of local charities as service providers. This paper captures the reactions of those working on the charity front line

    Differential binding patterns of anti-sulfatide antibodies to glial membranes

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    Sulfatide is a major glycosphingolipid in myelin and a target for autoantibodies in autoimmune neuropathies. However neuropathy disease models have not been widely established, in part because currently available monoclonal antibodies to sulfatide may not represent the diversity of anti-sulfatide antibody binding patterns found in neuropathy patients. We sought to address this issue by generating and characterising a panel of new anti-sulfatide monoclonal antibodies. These antibodies have sulfatide reactivity distinct from existing antibodies in assays and in binding to peripheral nerve tissues and can be used to provide insights into the pathophysiological roles of anti-sulfatide antibodies in demyelinating neuropathies

    The effects of passing speed distribution on rail corrugation growth rate

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    The transportation phenomenon known as wear-type rail corrugation is a significant problem in railway engineering, which manifests as a periodic wear pattern developing on the surface of the wheel and rail with use. Some field studies and recent theoretical results by the current authors have suggested that uniformity in pass speed causes an increase in corrugation growth rate. This paper presents the predicted change in corrugation growth rate and dominant wavelengths with change in passing speed distribution, based on state of the art cornering growth modelling techniques

    Contriibutors to the March Issue/Notes

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    Notes by Robert J. Callahan, John Kelly, William A. Meehan, Joseph R. Rudd, Arthur M. Diamond, John J. Doyle, Robert E. Sullivan, Roger Gustafson, William F. Martin, Robert A. Macdonell, Robert E. Million, Arthur A. May, and John F. Power

    A novel cellular pathway of antigen presentation and CD4 T cell activation in vivo

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    Dendritic cell activation of CD4 T cells in the lymph node draining a site of infection or vaccination is widely considered the central event in initiating adaptive immunity. The accepted dogma is that this occurs by stimulating local activation and antigen acquisition by dendritic cells, with subsequent lymph node migration, however the generalizability of this mechanism is unclear. Here we show that in some circumstances antigen can bypass the injection site inflammatory response, draining freely and rapidly to the lymph nodes where it interacts with subcapsular sinus (SCS) macrophages resulting in their death. Debris from these dying SCS macrophages is internalized by monocytes recruited from the circulation. This coordinated response leads to antigen presentation by monocytes and interactions with naïve CD4 T cells that can drive the initiation of T cell and B cell responses. These studies demonstrate an entirely novel pathway leading to initiation of adaptive immune responses in vivo
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