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191.
Unilateral renal artery plication in dogs reduced renal blood flow by 80% and produced a sustained elevation in arterial pressure whereas plasma renin activity increased for only 4 days. Sodium was retained for 3 days after plication, but this response is similar to that after a sham operation. Of seven dogs studied chronically, elevated arterial pressure was sustained for 27 days or longer in six animals. In three dogs hypertension continued for 2 mo before collateral vessels developed and arterial pressure fell; ligation of these collaterals restored hypertension. Arterial pressure was unaffected by an infusion of [1-sarcosine, 8-alanine] angiotensin II in chronic hypertensive dogs on a normal sodium intake. This angiotensin antagonist lowered arterial pressure after sodium depletion, but became ineffective following rapid sodium repletion. Chronic hypertensive dogs showed normal responses to deoxycorticosterone acetate. These findings suggest that the renin-angiotensin system is not critically involved in maintenace of chronic two-kidney renovascular hypertension in the dog. The data also show that the homeostatic role played by the renin-angiotensin system in the maintenance of arterial pressure remained intact in chronic hypertension.  相似文献   
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Recent evidence has indicated that physician judgments of patients can be influenced by contextual factors. This study examined three contextual factors relevant to hypothetical patients with low back pain, using vignettes that were varied in a 2 x 2 x 2 factorial design: level of reported pain (high vs low), level of supporting medical evidence (high vs low), and the valence of the physician-patient interaction (positive vs negative). Perceived levels of pain, disability, emotional distress, and somatic preoccupation were rated by internists after reading a vignette. Ratings of pain and disability were lower for patients without supporting medical evidence; ratings of distress, somatic preoccupation, and disability were greater for patients who exhibited negative rather than positive affect; internist ratings of pain were lower than patient ratings among patients reporting high levels of pain, while ratings were inflated for patients with low levels of pain. The results suggest that characteristics of both the patient and the situation may influence medical judgments.  相似文献   
194.
The d.c. and a.c. (100 Hz–1 MHz) conductivities of HCl-doped polyaniline have been measured in the temperature range 77–300 K. At 77 K, the a.c. conductivity data, (), can be described by the relation ()=As, where the parameter s lies close to unity and decreases with increase in the doping level. The ratio of measured a.c. to d.c. conductivity shows dispersion at 77 K, which decreases with increase in the doping level. This decrease is found to be sharp around pH3.0. In the temperature range 77–150 K, the observed d.c. conductivity data can be described by Mott's three dimensional variable range hopping (VRH) model. Scanning electron microscopy studies reveal a sharp change in structural morphology of HCl-doped polyaniline at a pH3.0. A strikingly remarkable structural morphology has been observed in the formc of a channel at this pH value. This change is accompanied by a rapid increase in d.c. conductivity, dielectric constant, along with sharp changes in structural morphology, which indicates the existence of a doping-induced structural conductivity correlation in this system. © 1998 Chapman & Hall  相似文献   
195.
Tyrosine hydroxylase (TyrOH) catalyzes the conversion of tyrosine to L-DOPA, the rate-limiting step in the biosynthesis of the catecholamines dopamine, adrenaline, and noradrenaline. TyrOH is highly homologous in terms of both protein sequence and catalytic mechanism to phenylalanine hydroxylase (PheOH) and tryptophan hydroxylase (TrpOH). The crystal structure of the catalytic and tetramerization domains of TyrOH reveals a novel alpha-helical basket holding the catalytic iron and a 40 A long anti-parallel coiled coil which forms the core of the tetramer. The catalytic iron is located 10 A below the enzyme surface in a 17 A deep active site pocket and is coordinated by the conserved residues His 331, His 336 and Glu 376. The structure provides a rationale for the effect of point mutations in TyrOH that cause L-DOPA responsive parkinsonism and Segawa's syndrome. The location of 112 different point mutations in PheOH that lead to phenylketonuria (PKU) are predicted based on the TyrOH structure.  相似文献   
196.
The complaint of hand cramps is common among patients who consult the neurologist or the hand surgeon. Classic writer's cramp is best characterized as a focal dystonia, and electromyographic studies reveal a characteristic pattern of cocontraction of the agonist and antagonist muscles of the forearm and hand. Although the outcome of treatment in the past has been unsatisfying, recent experience with new pharmacologic therapy, such as injections of botulinum toxin, has produced promising results. Further experience and improvement in this area will likely increase the therapeutic success in the treatment of writer's cramp and other focal dystonias.  相似文献   
197.
Wavelength Conversion Placement in WDM Mesh Optical Networks*   总被引:1,自引:0,他引:1  
Wavelength conversion helps improve the performance of wavelength division multiplexed (WDM) optical networks that employ wavelength routing. In this paper, we address the problem of optimally placing a limited number of wavelength converters in mesh topologies. Two objective functions, namely, minimizing the average blocking probability and minimizing the maximum blocking probability over all routes, are considered. In the first part of the paper, we extend an earlier analytical model to compute the blocking probability on an arbitrary route in a mesh topology, given the traffic and locations of converters. We then propose heuristic algorithms to place wavelength converters, and evaluate the performance of the proposed heuristics using the analytical model. Results suggest that simple heuristics are sufficient to give near-optimal performance.  相似文献   
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The ability of receptors (R) to activate G-proteins (G) is promoted by the binding of agonists, reflecting their induction of a receptor conformation which facilitates both the formation of a RG complex and guanine nucleotide exchange. Recent evidence from isolated membrane studies has indicated, however, that some receptors have the inherent ability to form RG complexes and promote GDP/GTP exchange in their unoccupied state. These receptors preferentially activate pertussis toxin-sensitive G-proteins (i.e. Gi/G(o)) and the interactions of R and G are modulated by monovalent cations (most notably Na+) both in the unoccupied and agonist-occupied states. Basal G-protein activation by such receptors is reduced both by increasing levels of cation and by antagonists which may act by inducing receptor conformations which are less favorable for RG complexation. This behaviour conforms to the predictions of a ternary complex model of receptor function and can be considered in structural terms for those receptors such as the alpha-2 adrenergic receptor where ligand binding and G-protein activation regions have been proposed.  相似文献   
200.
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