Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Intracranial membrane

The reciprocal tension membrane (RTM) refers to the function ofthe mobility of intracranial and intraspinal membranes, the pia, arachnoid, and dura. Understanding the development and the anatomy of the membranes helps illustrate their function (see Section X, Chapter 102). The intracranial membranes are intimately related to the fascia throughout the rest of the body. [Pg.110]

Membranous structures in the body are all composed of coimective tissue derived from embryonic mesenchyme. AU membranes are continuous with all other mesenchymally derived connective tissues of the body. The intracranial membranes are intimately related to the fascias of the rest of the body through foramina in the cranial base and throughout the entire spine, the foramen magnum, and all fascial attachments to the undersurface of the cranial base. [Pg.550]

As described above, because MAO is bound to mitochondrial outer membranes, MAOIs first increase the concentration of monoamines in the neuronal cytosol, followed by a secondary increase in the vesicle-bound transmitter. The enlarged vesicular pool will increase exocytotic release of transmitter, while an increase in cytoplasmic monoamines will both reduce carrier-mediated removal of transmitter from the synapse (because the favourable concentration gradient is reduced) and could even lead to net export of transmitter by the membrane transporter. That MAOIs increase the concentration of extracellular monoamines has been confirmed using intracranial microdialysis (Ferrer and Artigas 1994). [Pg.433]

The ACE gene encodes two isozymes (somatic ACE isozyme and germinal ACE isozyme). ACE is a membrane-bound enzyme on the surface of vascular endothelial cells that also circulates in plasma and shows great individual variability determined by an I/D polymorphism in intron 16 of the ACE gene (ACE-I/D polymorphism). More than 160 ACE polymorphisms have been reported, 34 of which are located in coding regions, and 18 are missense mutations (606). ACE-related polymorphic variants have been associated with hypertension, atherosclerosis, stroke, left ventricular hypertrophy, chronic renal failure in IgA nephropathy, Henoch-Schonlein purpura nephritis, mechanical efficiency of skeletal muscle, intracranial aneurysms, susceptibility to myocardial infarction, diabetic nephropathy, AD, and longevity (12,606,607). [Pg.312]

A 13-year-old boy underwent a 17-hour craniotomy in an attempt to resect an arteriovenous malformation with propofol-based anesthesia. He developed frank propofol infusion syndrome after 74 hours of postoperative propofol sedation in the neurosurgical ICU (used to manage intracranial hypertension). Echocardiography showed severe biventricular dysfunction despite extraordinary pharmacological support. Extracorporeal circulation with membrane oxygenation (ECMO) was instituted at the bedside via cannulation of the left femoral vessels. Hemofiltration... [Pg.640]

Headache is most common side effect severe headache may be sign of pseudotumor cerebri (intracranial hypertension) "ATRA syndrome" pulmonary symptoms (dyspnea, respiratory distress, fever, pleural effusions) low emetogenic potential dry skin and mucous membranes, mucositis bone pain transient elevations in transaminases, bilirubin... [Pg.2315]

Lidocaine (Xylocaine) Ionized form of drug temporarily reduces the permeability of neuronal membranes to sodium. Thus, action potentials cannot be generated or propagated. All types of injection and topical anesthesia, sedation, arrhythmias (Table 4.7A), intracranial hypertension. Drowsiness, dizziness, heart block, arrhythmias, hypotension. [Pg.32]

The highly charged complex, ruthenium red (Structure 59, Chapter 6) is a powerful and specific inhibitor of calcium transport across mitochondrial membranes [16, 17], similar to the inhibition induced by lanthanides [18]. Significant amounts of the complex may also penetrate into nerve fibers in vivo and in vitro, and induce neurotoxicity [19, 20]. Interestingly, the toxicity is dependent on the route of administration intracranial administration produces convulsions while intraperitioneal injection induces paralysis [21]. [Pg.259]

The mobility of the intracranial and intraspi-nal membranes and the function of the reciprocal tension membrane... [Pg.109]

The Mobility of the Intracranial and Intraspinal Membranes and the Function of the Reciprocal Tension Membrane... [Pg.110]

THE INTRACRANIAL AND INTRASPINAL MEMBRANES AND THE RECIPROCAL TENSION MEMBRANE... [Pg.550]


See other pages where Intracranial membrane is mentioned: [Pg.393]    [Pg.68]    [Pg.563]    [Pg.31]    [Pg.252]    [Pg.399]    [Pg.57]    [Pg.223]    [Pg.2538]    [Pg.1517]    [Pg.250]    [Pg.994]    [Pg.327]    [Pg.183]    [Pg.173]    [Pg.329]    [Pg.509]    [Pg.554]    [Pg.1563]   
See also in sourсe #XX -- [ Pg.549 , Pg.550 , Pg.551 ]




SEARCH



Intracranial

© 2024 chempedia.info