Relevant bibliographies by topics / Push-pull perfusion

Academic literature on the topic 'Push-pull perfusion'

Author: Grafiati
Published: 10 December 2022
Last updated: 28 January 2023

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Journal articles on the topic "Push-pull perfusion"

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Kottegoda, Sumith, Imtiazuddin Shaik, and Scott A. Shippy. "Demonstration of low flow push–pull perfusion." Journal of Neuroscience Methods 121, no. 1 (November 2002): 93–101. http://dx.doi.org/10.1016/s0165-0270(02)00245-5.

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Ojeda-Torres, G., L. Williams, D. E. Featherstone, and S. A. Shippy. "Sample collection and amino acids analysis of extracellular fluid of mouse brain slices with low flow push–pull perfusion." Analyst 140, no. 19 (2015): 6563–70. http://dx.doi.org/10.1039/c5an00805k.

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Gliessman, P. M., K. Y. Pau, J. D. Hill, and H. G. Spies. "Chronic push-pull brain perfusion in unrestrained rhesus macaques." Journal of Applied Physiology 61, no. 6 (December 1, 1986): 2273–79. http://dx.doi.org/10.1152/jappl.1986.61.6.2273.

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A system was developed to permit perfusion of local brain regions and simultaneous peripheral blood sampling in free-moving caged monkeys. The system comprises a calvarial headpiece that contains multiple push-pull cannulas (PPC), a flexible stainless steel tether, a four-channel fluid swivel, and a surgical procedure for simultaneous multisite brain cannulation. Rhesus macaques were fitted surgically with an indwelling jugular catheter and PPC directed into the third ventricle, median eminence, and preoptic area. These animals were tethered for periods of 14–70 h during which brain perfusates and peripheral blood samples were collected at 10- to 30-min intervals through the tether-swivel assembly. Levels and pulsatile patterns of gonadotropin-releasing hormone in 10-min perfusate samples and luteinizing hormone and cortisol in sequential plasma samples were quantified by specific radioimmunoassays. The normal endocrine profiles in these animals suggest that this system provides a valuable method to study patterns of neurosecretions in an unrestrained simian.
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Singh, Ava V., and Howard R. Morris. "An HPLC/push-pull perfusion technique for investigating peptide metabolism." Biochemical and Biophysical Research Communications 130, no. 1 (July 1985): 37–42. http://dx.doi.org/10.1016/0006-291x(85)90378-x.

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Wolf, Rainer, Ursula Tscherne, and Hinderk M. Emrich. "Suppression of preoptic GABA release caused by push-pull-perfusion with sodium valproate." Naunyn-Schmiedeberg's Archives of Pharmacology 338, no. 6 (December 1988): 658–63. http://dx.doi.org/10.1007/bf00165631.

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Cox, P. S., D. A. Denton, D. R. Mouw, and E. Tarjan. "Natriuresis induced by localized perfusion within the third cerebral ventricle of sheep." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 252, no. 1 (January 1, 1987): R1—R6. http://dx.doi.org/10.1152/ajpregu.1987.252.1.r1.

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Push-pull perfusion was performed at four different sites in the third cerebral ventricle of conscious sheep. The recovery of the infused solution was 75–90%, suggesting a localized change in the ionic composition and osmolality restricted to a relatively small area in the cerebrospinal fluid (CSF). Sodium and potassium excretion and urine flow were studied before, during, and after perfusion of 200, 150, and 100 mM Na-CSF. Localized perfusion in the anterior dorsal third ventricle (AD3V) of 200 mM Na-CSF caused an increase in sodium and potassium excretion, in urine flow, and a decrease in free water clearance. Perfusion of 200 mM Na-CSF at the other three perfusion sites, i.e., anterior ventral third ventricle, posterior dorsal third ventricle, and posterior ventral third ventricle, did not influence sodium excretion and urine flow. Perfusions with 150 and 100 mM Na-CSF did not cause any change in sodium, potassium excretion, or urine flow at any of the four perfusion sites. These results suggest that sensors sensitive to changes of sodium concentration are located close to the ventricular surface in the anterior dorsal part of the third cerebral ventricle. When stimulated with increased sodium concentration they will initiate increased sodium excretion.
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Rupert, Amy E., Y. Ou, M. Sandberg, and S. G. Weber. "Assessment of Tissue Viability Following Electroosmotic Push–Pull Perfusion from Organotypic Hippocampal Slice Cultures." ACS Chemical Neuroscience 4, no. 5 (May 2, 2013): 849–57. http://dx.doi.org/10.1021/cn4000814.

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Myers, R. D., and Leslie Gurley-Orkin. "New “micro push-pull” catheter system for localized perfusion of diminutive structures in brain." Brain Research Bulletin 14, no. 5 (May 1985): 477–83. http://dx.doi.org/10.1016/0361-9230(85)90026-7.

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RAMIREZ, V. D., J. C. CHEN, E. NDUKA, W. LIN, and A. D. RAMIREZ. "Push-Pull Perfusion of the Hypothalamus and the Caudate Nucleus in Conscious, Unrestrained Animals." Annals of the New York Academy of Sciences 473, no. 1 Neurochemical (December 1986): 434–47. http://dx.doi.org/10.1111/j.1749-6632.1986.tb23634.x.

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Myers, R. D., Amir H. Rezvani, and L. A. Gurley-Orkin. "New double-lumen polyethylene cannula for push-pull perfusion of brain tissue in vivo." Journal of Neuroscience Methods 12, no. 3 (January 1985): 205–18. http://dx.doi.org/10.1016/0165-0270(85)90003-2.

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Dissertations / Theses on the topic "Push-pull perfusion"

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Favre, de Thierrens Carle. "Contribution à l'étude de l'incidence des molécules-signaux du système neuro-endocrinien dans la physiopathologie odontologique : apport de la technique de "perfusion push-pull modifiée" à l'étude in vivo des prostaglandines et des enképhalines pulpaires ; détection et quantification radioimmunologique de somatostatine-IR dans la pulpe dentaire du rat." Montpellier 1, 1996. http://www.theses.fr/1996MON12200.

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黃靖雯. "Online In-tube Solid Phase Extraction Coupled with Push-pull Perfusion Sampling and ICP-MS Determination for in vivo Monitoring Extracellular Silver anoparticles in Rat Liver." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/48198763158913686798.

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Abstract:
碩士
國立清華大學
生醫工程與環境科學系
98
Recently, the massive progression of nanotechnology has led a large number of applications and consumer goods. Around 50% of nanotechnology-based consumer products were made of silver nanoparticles (AgNPs), making them applicable to wound dressings, socks, and food containers due to the effective inhibition of growth in various microorganisms. Being applied for human use, however, the biokinetic and risk of AgNPs in mammal were rarely assessed, because there is still lack of an adequate analytical technique can provide dynamic information of AgNPs in mammal up to now. To in vivo monitoring of AgNPs in the extracellular fluids of rat liver, we developed an unsophisticated, automatic, and online hyphenated system comprising push-pull perfusion (PPP) sampling, the established in-tube solid phase extraction (SPE) procedure, and inductively coupled plasma mass spectrometry (ICP-MS) in this study. This system takes advantage of adsorbing AgNPs onto the inner wall of polytetrafluoroethylene (PTFE) tubing which means AgNPs can be extracted from the complicated biological matrix. To optimize the analytical performance, the effect of sampling flow rate, sample loading flow rate, sample pH, tubing inner diameter and blood matrix were investigated. It has been demonstrated that under the optimized conditions, the detection limit of analyte AgNPs were found in the range of sub–?慊/L. The accuracy of our proposed system was confirmed by analyzing biological samples spiking with defined amounts of AgNPs to demonstrate its validity. After the validation of this method, the applicability of our developed system was further demonstrated by in vivo monitoring the dynamic variation in the concentrations of AgNPs in the liver of anesthetized rats after intravenous dosing.
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Books on the topic "Push-pull perfusion"

1

D, Myers R., Knott Peter J, and New York Academy of Sciences., eds. Neurochemical analysis of the conscious brain: Voltammetry and push-pull perfusion. New York, N.Y: New York Academy of Sciences, 1986.

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2

Myers, Robert D., and Peter J. Knott. Neurochemical Analysis of the Conscious Brain: Voltammetry and Push-Pull Perfusion (Annals of the New York Academy of Sciences, Vol 473). New York Academy of Sciences, 1986.

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Book chapters on the topic "Push-pull perfusion"

1

RAMÍREZ, VICTOR D. "The Push—Pull Perfusion Technique in Neuroendocrinology." In In Vivo Perfusion and Release of Neroactive Substances, 249–70. Elsevier, 1985. http://dx.doi.org/10.1016/b978-0-12-083350-4.50020-0.

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Shippy, Scott A., and Geovannie Ojeda-Torres. "PUSH–PULL PERFUSION SAMPLING OF THIN NEURONAL TISSUES." In Compendium of In Vivo Monitoring in Real-Time Molecular Neuroscience, 321–35. WORLD SCIENTIFIC, 2017. http://dx.doi.org/10.1142/9789813220546_0014.

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SCHOENER, EUGENE P. "Neuronal Responses to Neuroactive Substances Administered by Push—Pull Perfusion." In In Vivo Perfusion and Release of Neroactive Substances, 25–39. Elsevier, 1985. http://dx.doi.org/10.1016/b978-0-12-083350-4.50008-x.

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REDGRAVE, PETER. "Technical Issues Associated with Push—Pull Perfusion in Unanesthetized and Unrestrained Animals." In In Vivo Perfusion and Release of Neroactive Substances, 11–23. Elsevier, 1985. http://dx.doi.org/10.1016/b978-0-12-083350-4.50007-8.

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IIJIMA, TOSHIHIKO, and KAZUO NUNOKI. "Superfusion and Electrical Stimulation of the Canine Brain with a Push—Pull Cannula." In In Vivo Perfusion and Release of Neroactive Substances, 41–49. Elsevier, 1985. http://dx.doi.org/10.1016/b978-0-12-083350-4.50009-1.

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VELASCO, MARCOS, FRANCISCO VELASCO, MARÍATRINIDAD PACHECO, and FRANCISCO ESTRADA-VILLANUEVA. "The Efficacy of the Push—Pull Perfusion Technique in the Study of Sleep, Epilepsy, and Tremor." In In Vivo Perfusion and Release of Neroactive Substances, 271–91. Elsevier, 1985. http://dx.doi.org/10.1016/b978-0-12-083350-4.50021-2.

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PHILIPPU, ATHINEOS. "The Use of Push—Pull Cannulae for Superfusing Various Hypothalamic Areas in Anesthetized and Conscious, Freely Moving Animals." In In Vivo Perfusion and Release of Neroactive Substances, 221–32. Elsevier, 1985. http://dx.doi.org/10.1016/b978-0-12-083350-4.50018-2.

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VANDER HEYDEN, JAN A. M., KOR VENEMA, and JAKOB KORF. "Push—Pull Perfusion Studies on the in Vivo Release of Endogenous Transmitter and Nontransmitter Amino Acids in the Rat Brain." In In Vivo Perfusion and Release of Neroactive Substances, 51–68. Elsevier, 1985. http://dx.doi.org/10.1016/b978-0-12-083350-4.50010-8.

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BAYÓN, ALEJANDRO, SARA SOLANO, BENITO ANTÓN, IRENE CASTAÑO, and DAVID DÍAZ-PONTONES. "Push—Pull Perfusion Studies on the in Vivo Release of Proteins, Enzymes, and the Neuroactive Peptides—Enkephalins from the Rat Brain." In In Vivo Perfusion and Release of Neroactive Substances, 69–93. Elsevier, 1985. http://dx.doi.org/10.1016/b978-0-12-083350-4.50011-x.

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MARTIN, GREGORY E., and DEAN R. HAUBRICH. "The Use of Push—Pull Perfusion Techniques for Measuring the Efflux of [3H]Dopamine in the Striatum of the Conscious Rat." In In Vivo Perfusion and Release of Neroactive Substances, 293–314. Elsevier, 1985. http://dx.doi.org/10.1016/b978-0-12-083350-4.50022-4.

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