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Development, of brain

Abnormal Brain Development. In a certain sense, neurodegenerative disorders reside at the opposite end of the spectrum from the so-called neurodevelopmental diseases. These result from abnormal development of brain circuitry. The causes of... [Pg.22]

In SUMMARY, it would appear that a detailed knowledge of the pharmacokinetics of the main groups of psychotropic drugs is only of very limited clinical use. This is due to limitations in the methods for the detection of some drugs (e.g. the neuroleptics), the presence of active metabolites which make an important contribution to the therapeutic effect, particularly after chronic administration (e.g. many antidepressants, neuroleptics and anxiolytics), and the lack of a direct correlation between the plasma concentration of the drug and its therapeutic effect. Perhaps the only real advances will be made in this area with the development of brain imaging techniques whereby the concentrations of the active drug in the... [Pg.99]

Another commercially available product containing naturally occurring marine products is Formulaid , produced by Martek Biosciences as a nutritional supplement for infant formulas. Formulaid contains two fatty acids, arachidonic acid (ARA) and docosahexaenoic acid (DHA), extracted from a variety of marine microalgae. ARA and DHA are the most abundant polyunsaturated fatty acids found in breast milk, and they are the most important fatty acids used in the development of brain gray matter. They are especially desirable for use in infant formulas because they come from nonmeat sources and can be advertised as vegetarian additives to the product. [Pg.32]

The recent addition of interferon-P-la and interferon-pib to the therapeutic arsenal for the treatment of MS aims to shut down inflammation at the blood-brain barrier and thereby reduce the rate of relapse and decrease frequency and severity of MS disease symptoms.Both P-interferons have demonstrated benefits in the treatment of patients with established MS, including slowing the progression of physical disability, reducing the rate of clinical relapses, and reducing the development of brain lesions, as assessed by MRI. Several trials have found that interferon-pib (Betaseron) reduced the frequency of relapse by approximately 30% [3-5]. These studies also suggested a trend toward a delay in the progression of disability. Interferon-pia (Avonex) was subsequently found to reduce the frequency of relapse [6-8]. [Pg.186]

Before the development of brain imaging techniques, neuroanatomical correlates were primarily related to structural lesions of the CNS. Despite the fact that abnormalities have been found in both schizophrenia and affective illness, interest in the neuropathology of mood disorders has not been as intense as for schizophrenia. [Pg.190]

In summary, neonatal RSD produces adult depression-like changes and behavioral changes beyond depression. In general, neonatal RSD slows the overall development of brain and behavior. At the cellular and molecular levels, neonatal RSD yields the immature features of a low-waking capacity and less voluntary movements. [Pg.136]

Hilakivi LA, Taira T, Hilakivi I, MacDonald E, Tuomisto L, Hellevuo K. Early postnatal treatment with propranolol affects development of brain amines and behavior. Psychopharmacology 1988 96 353-359. [Pg.146]

Effects of drugs on development of brain receptors and neurochemistry... [Pg.282]

V. Nair, Prenatal exposure to drugs Effect on the development of brain monoamine systems, in A. Vernadakis and N. Veiner (Eds.), Drugs and the Developing Brain, Plenum Press, New York, 1974, pp. 171-194. [Pg.309]

Betz A. L., Ennis S. R., and Schielke G. P. (1989) Blood-brain barrier sodium transport limits development of brain edema during partial ischemia in gerbils. Stroke 20,1253-1259. [Pg.76]

Human CEC cultured on filter inserts can be used to measure brain penetration of drugs to make in vitro-in vivo correlations. They can further be used to study for example brain inflammation that has been implicated in the development of brain edema and secondary brain damage in ischemia and trauma. Zhang et al. (2000) studied leukocyte infiltration across the blood-brain barrier and showed the expression of adhesion molecules and leukocyte chemoattractants under ishemia in vitro conditions. [Pg.528]

Amiry-Moghaddam M, Xue R, Haug FM, Neely JD, Bhardwaj A, Agre P, Adams ME, Froehner SC, Mori S, Ottersen OP (2004) Alpha-syntrophin deletion removes the perivascular but not endotheUeil pool of aquaporin-4 at the blood-brain barrier and delays the development of brain edema in an experimenUil model of acute hyponatremia. FASEB J 18 542-544 Anderson CM, Nedeigaard M (2003) Astrocyte-mediated control of cerebral microcirculation. Trends Neurosci 26 340-345... [Pg.156]

Kozniewska E, Roberts TP, Tsuura M, Mintorovitch J, Moseley ME, Kucharczyk J (1995) NG-nitro-L-arginine delays the development of brain injuty during focal ischemia in rats. Stroke 26 282-289... [Pg.161]

Jones LS, Gauger LL, Davis JN, Slotkin TA, Bartolome JV. Postnatal development of brain a,-adrenergic receptors in vitro autoradiography with [125I] HEAT in normal rats and rats treated with a-difluoromethylornithine, a specific, irreversible inhibitor of ornithine decarboxylase. Neuroscience 1985 15 1195-1202. [Pg.199]

It seems reasonable to assume that, from a functional point of view, the appearance of species with the ability to acquire drives for unnatural goals was the last radical turning-point in the development of brain organization. In the animal kingdom the new mechanism reached its functionally most sophisticated level in the group of anthropoid apes, but it reached perfection in Homo sapiens only. The new mechanism culminated in the development of speech - the classic, human-specific instrument that made interpersonal communication possible by capturing reality in the form of symbols - and thus opened the way for the operation of an unrestricted variety of acquired drives. [Pg.54]

Lipoxygenase (5LO) is upregulated in AD, and plays an active role in the development of brain amyloidosis in the APP transgenic mice. APP transgenic mice treated with Zileuton, a specific 5LO inhibitor, showed memory improvement reduction of Ap levels and deposition, secondary to a downregulation of the y-secretase pathway. Zileuton-treated mice had a reduction in tau phosphorylation, secondary to a decreased activation ofthe cdk5 kinase [558],... [Pg.457]

Zivadinov R, Zorzon M. Is gadolinium enhancement predictive of the development of brain atrophy in multiple sclerosis A review of the hterature. J Neuroimag 2002 12 302-309. [Pg.1019]

Belmonte MK, AUen G, Beckel-Mitchener A, Boulanger LM, Carper RA, Webb SJ (2004) Autism and abnormal development of brain connectivity. J Neurosci 24 9228-9231. [Pg.181]


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Developing brain

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