PubMed Health⌕ Search

Biomedical subjects

R Pape

Publications and source records attributed to R Pape.

At least 19 recordsLinked to original sources
PubMed2005

Delayed inhibition of Nogo-A does not alter injury-induced axonal sprouting but enhances recovery of cognitive function following experimental traumatic brain injury in rats.

Traumatic brain injury causes long-term neurological motor and cognitive deficits, often with limited recovery. The inability of CNS axons to regenerate following traumatic brain injury may be due, in part, to inhibitory molecules associated with myelin. One of these myelin-associated proteins, Nogo-A, inhibits neurite outgrowth in vitro, and inhibition of Nogo-A in vivo enhances axonal outgrowth and sprouting and improves outcome following experimental CNS insults. However, the involvement of Nogo-A in the neurobehavioral deficits observed in experimental traumatic brain injury remains unknown and was evaluated in the present study using the 11C7 monoclonal antibody against Nogo-A. Anesthetized, male Sprague-Dawley rats were subjected to either lateral fluid percussion brain injury of moderate severity (2.5-2.6 atm) or sham injury. Beginning 24 h post-injury, monoclonal antibody 11C7 (n=17 injured, n=6 shams included) or control Ab (IgG) (n=16 injured, n=5 shams included) was infused at a rate of 5 microl/h over 14 days into the ipsilateral ventricle using osmotic minipumps connected to an implanted cannula. Rats were assessed up to 4 weeks post-injury using tests for neurological motor function (composite neuroscore, and sensorimotor test of adhesive paper removal) and, at 4 weeks, cognition was assessed using the Morris water maze. Hippocampal CA3 pyramidal neuron damage and corticospinal tract sprouting, using an anterograde tracer (biotinylated dextran amine), were also evaluated. Brain injury significantly increased sprouting from the uninjured corticospinal tract but treatment with monoclonal antibody 11C7 did not further increase the extent of sprouting nor did it alter the extent of CA3 cell damage. Animals treated with 11C7 showed no improvement in neurologic motor deficits but did show significantly improved cognitive function at 4 weeks post-injury when compared with brain-injured, IgG-treated animals. To our knowledge, the present findings are the first to suggest that (1) traumatic brain injury induces axonal sprouting in the corticospinal tract and this sprouting may be independent of myelin-associated inhibitory factors and (2) that post-traumatic inhibition of Nogo-A may promote cognitive recovery unrelated to sprouting in the corticospinal tract or neuroprotective effects on hippocampal cell loss following experimental traumatic brain injury.

Analysis of Variance↗
PubMed1996

[A Trojan horse in nursing? Nursing diagnosis and its theoretical context].

Nursing diagnosis and their theoretical context. The necessity of developing and using nursing diagnoses is indisputable. In the process of the professionalisation of nursing they constitute a fundamental aspect of nursing science. However, if nursing diagnoses are not to harm nursing, they must be developed with care. One difficulty will be to translate the theoretical framework in its abstract form into realisable elements in practice. For this purpose the nursing related terminology must be unambiguous and understandable. Nursing must seek the discussion with allied sciences. Nurses must develop their cognitive skills to ensure a valid use of nursing diagnoses. The areas common with other occupational groups in the treatment process have to be classified and their contents have to be determined. This is a challenge to colleagues in all areas of work and indifferent functions to participate in this development. It is also a challenge to nursing science itself.

Clinical Competence↗
PubMed1990

Secretory organelle docking at the cell membrane of Paramecium cells: dedocking and synchronized redocking of trichocysts.

We present the first evidence that secretory organelle docking at the cell membrane can be reversed in vivo. In nondischarge (nd) mutants of Paramecium tetraurelia all trichocysts can be detached from the cell surface within 2-3 h by different means, including cytochalasin B (but not D), high cell density, or Ca2+ ionophores. Considering the well-established ultrastructural differences between nd and wild-type (wt) cells, one can conclude that trichocyst docking at the cell periphery involves two docking sites (I, II): Site I ties the organelles to the epiplasm, and site II is the connection to the cell membrane at the fusogenic zone (expressed only in wt cells); both sites are close to the cell surface and only 150 nm apart. When the trigger for detachment of cortically docked trichocysts (high cell density, cytochalasin B) is relieved, trichocysts are synchronously reattached at the cell membrane, within 40-50 min, with a rate of 20-40 organelles/min, which far exceeds spontaneous docking rates. This is therefore also the first report on synchronization of secretory organelle docking. It is shown by radioactive leucine labeling that the same organelles are redocked, because trichocyst biogenesis is minimal under the conditions of de/redocking used. Surprisingly not only redocking but also detachment of trichocysts from the cell surface can be abolished by inhibitors of protein synthesis. Since Ca2+ ionophores mimic the effects of other conditions sufficient to detach trichocysts from the cell surface, we assume that a protein-dependent mechanism sensitive to Ca2+ (or other ions in exchange) may operate in trichocyst detachment. The precise mechanism involved in attachment or detachment of trichocysts remains to be elucidated.

Animals↗
PubMed1988

Antihypertensive thiadiazoles. 1. Synthesis of some 2-aryl-5-hydrazino-1,3,4-thiadiazoles with vasodilator activity.

Some 2-aryl-5-hydrazino-1,3,4-thiadiazoles have been synthesized and screened for antihypertensive activity. In general, compounds with a 2-substituted phenyl ring had higher activity than their 3- or 4-substituted counterparts or those containing heteroaryl groups. The 2-methylphenyl and 2-ethylphenyl derivatives 7 and 18 were the most potent members of the series. Preliminary studies indicated that the hypotensive action of these compounds was due to a direct relaxant effect on vascular smooth muscle.

Animals↗
PubMed1988

Antihypertensive thiadiazoles. 2. Vasodilator activity of some 2-aryl-5-guanidino-1,3,4-thiadiazoles.

Some 2-aryl-5-guanidino-(or N-substituted guanidino)-1,3,4-thiadiazoles and closely related analogues were found to lower blood pressure in metacorticoid (DOCA) hypertensive rats. In the unsubstituted guanidines that exhibited low toxicity, optimum activity resulted when the aryl group was a 2-methylphenyl ring (11). Modifications to the guanidine group did not increase antihypertensive activity, but, in the 2-methylphenyl series, the N-n-butyl- and N-(2-methoxyethyl)guanidines (63 and 78) and the related iminoimidazolidine 93 were of comparable activity to that of the unsubstituted guanidine 11. The iminoimidazolidine 93 showed a somewhat longer duration of action than the guanidine derivatives. Preliminary studies in a pithed rat preparation indicated that these thiadiazole derivatives (11, 63, and 93) lowered blood pressure by a direct relaxant effect on vascular smooth muscle.

Animals↗
PubMed1986

[Holter ECG monitoring during peridural anesthesia with bupivacaine 0.75%].

Electrocardiographic monitoring was undertaken in thirteen women and seven men before, during, and after epidural anaesthesia with bupivacaine 0.75%. The average surveying time lasted 18:28 h. Bupivacaine 0.75% was given in a dose of 1.5 mg/kg body weight (n = 8) and 2 mg/kg body weight (n = 12). Eleven patients (8 female/3 male) = 55% showed VES of category I of the LOWN-classification. Three subjects (3 female) suffered VES before and after injection of bupivacaine 0.75%. Five patients (3 female/2 male) showed VES before and three (2 female/1 male) only after epidural blockade. Serious arrhythmias or other signs of toxic actions on the myocardium were not registered.

Anesthesia, Epidural↗
PubMed1985

Synchronous exocytosis in Paramecium cells. VI. Ultrastructural analysis of membrane resealing and retrieval.

After the synchronous induction of exocytosis of secretory organelles (trichocysts) in Paramecium tetraurelia cells the process of membrane resealing and retrieval could be followed under synchronous conditions. The characteristic aggregates of membrane intercalated particles (MIPs) contained within the freeze-fractured cell membrane (rings and rosettes) and trichocyst membranes (annulus MIPs), in addition to collar striations on the top of trichocyst membranes, served as endogenous ultrastructural markers. This allowed us to follow the re-arrangement of membrane constituents during and after exocytosis with high temporal and spatial precision. Membrane specificity is maintained to a considerable extent (approximately 99.5%), as judged from the rare occurrence of aberrant resealing (according to freeze-fracture data) and from the rather minute shift of glycocalyx components (according to electron staining experiments) during normal membrane resealing. Coated pits are not involved in membrane retrieval (155 ghosts analysed); since the membrane regions involved in exocytotic fusion are backed by apposed materials, probably proteins, this may restrain membrane constituents from intermixing. Another factor for maintaining membrane specificity is the fact that resealing of the exocytotic opening occurs much more rapidly than in most other systems. The retrieval operates with a half-life of 3 (strain 7S) to 9 min (K401); the involvement of cortical microtubules in the retrieval can be largely excluded, since only two microtubules (of unidentified origin) were seen to approach ghost structures in 4074 cases analysed during this period of intense ghost retrieval. Phalloidin microinjected at a dose that blocked all cytoplasmic streaming (before synchronous exocytosis was induced) did not abolish membrane resealing and retrieval, which, therefore, may be passive processes.

Animals↗
PubMed1985

Synchronous exocytosis in Paramecium cells. V. Ultrastructural adaptation phenomena during re-insertion of secretory organelles.

We used aminoethyldextran (AED) as a secretagogue for the simultaneous exocytosis of a great proportion of secretory organelles (trichocysts) from Paramecium tetraurelia cells and we applied freeze-fracturing and ultrathin sectioning for a quantitative analysis of the re-arrangement of ultrastructural details within the cell membrane during re-insertion of new trichocysts. Characteristic arrangements of membrane-intercalated particles (MIPs) occur over trichocyst docking sites: 300 nm large double rings of MIPs and a MIP rosette in the middle. Empty sites, displaying a compressed ring ("parenthesis") without a rosette, are expanded to full size rings when a trichocyst is docked. We obtained a first hint on the possible existence of a short lived (approximately 5 min) adaptation stage, represented by rings without a rosette. This could mean that docking of a trichocyst would induce the assembly of rosette MIPs over a newly docked trichocyst. The reformation of rosettes is paralleled by an increasing number of extrudable trichocysts which underscores the causal role of rosette MIPs in exocytosis performance. New trichocysts are inserted at the old predetermined sites after removal of ghosts and formation of a "plug" as a receptor-type structure. The number of non-docked, free trichocysts in the cytoplasm is only slightly changed, indicating a continuous synthesis and docking rate (approximately 2-3 organelles per min). Since in strain 7S ghosts are removed within approximately 10 min and docking goes on over 9 h, there occur many empty docking sites in the time period in between, with a maximum of approximately 1 h after AED triggering, thus providing a unique situation for further experiments.

Adaptation, Physiological↗