2,213 research outputs found

    Optical and X-ray Variability in The Least Luminous AGN, NGC4395

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    We report the detection of optical and X-ray variability in the least luminous known Seyfert galaxy, NGC4395. The featureless continuum changed by a factor of 2 in 6 months, which is typical of more luminous AGN. The largest variation was seen at shorter wavelengths, so that the spectrum becomes `harder' during higher activity states. In a one week optical broad band monitoring program, a 20% change was seen between successive nights. In a 1 month period the spectral shape changed from a power law with spectral index alpha ~0 (characteristic of quasars) to a spectral index alpha ~2 (as observed in other dwarf AGN). ROSAT HRI and PSPC archive data show a variable X-ray source coincident with the galactic nucleus. A change in X-ray flux by a factor \~2 in 15 days has been observed. When compared with more luminous AGN, NGC4395 appears to be very X-ray quiet. The hardness ratio obtained from the PSPC data suggests that the spectrum could be absorbed. We also report the discovery of weak CaIIK absorption, suggesting the presence of a young stellar cluster providing of the order of 10% of the blue light. Using HST UV archive data, together with the optical and X-ray observations, we examine the spectral energy distribution for NGC4395 and discuss the physical conditions implied by the nuclear activity under the standard AGN model. The observations can be explained by either an accreting massive black hole emitting at about 10^(-3) L_(Edd) or by a single old compact SNR with an age of 50 to 500 yr generated by a small nuclear starburst.Comment: 19 pages, 9 figures, to appear in MNRA

    Dialysis residential care : a future dialysis service model

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    People with chronic kidney disease are ageing and have increasing co-morbidities. The current delivery of renal replacement therapy, dialysis and transplantation, needs to adjust to changing patient needs. This paper proposes a potential future service delivery model featuring a dialysis residential care facility and a care coordination focus. The residential care facility would be composed of four levels of care; high, hostel, independent and outpatient. The paper argues that this model may result in decreased morbidity, improved patient quality of life and may prove cost effective. Patients\u27 nutritional status, medication adherence and transport efficiency may be improved. We propose this model to stimulate further debate in order to meet the needs of current and future chronic kidney disease patients.<br /

    The Skeletal L-type Ca2+ Current Is a Major Contributor to Excitation-coupled Ca2+ entry

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    The term excitation-coupled Ca2+ entry (ECCE) designates the entry of extracellular Ca2+ into skeletal muscle cells, which occurs in response to prolonged depolarization or pulse trains and depends on the presence of both the 1,4-dihydropyridine receptor (DHPR) in the plasma membrane and the type 1 ryanodine receptor in the sarcoplasmic reticulum (SR) membrane. The ECCE pathway is blocked by pharmacological agents that also block store-operated Ca2+ entry, is inhibited by dantrolene, is relatively insensitive to the DHP antagonist nifedipine (1 μM), and is permeable to Mn2+. Here, we have examined the effects of these agents on the L-type Ca2+ current conducted via the DHPR. We found that the nonspecific cation channel antagonists (2-APB, SKF 96356, La3+, and Gd3+) and dantrolene all inhibited the L-type Ca2+ current. In addition, complete (>97%) block of the L-type current required concentrations of nifedipine >10 μM. Like ECCE, the L-type Ca2+ channel displays permeability to Mn2+ in the absence of external Ca2+ and produces a Ca2+ current that persists during prolonged (∼10-second) depolarization. This current appears to contribute to the Ca2+ transient observed during prolonged KCl depolarization of intact myotubes because (1) the transients in normal myotubes decayed more rapidly in the absence of external Ca2+; (2) the transients in dysgenic myotubes expressing SkEIIIK (a DHPR α1S pore mutant thought to conduct only monovalent cations) had a time course like that of normal myotubes in Ca2+-free solution and were unaffected by Ca2+ removal; and (3) after block of SR Ca2+ release by 200 μM ryanodine, normal myotubes still displayed a large Ca2+ transient, whereas no transient was detectable in SkEIIIK-expressing dysgenic myotubes. Collectively, these results indicate that the skeletal muscle L-type channel is a major contributor to the Ca2+ entry attributed to ECCE
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