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Brain cell proliferation

In summary, there is incontrovertible evidence that antidepressants cause suicidality, irritability, violence, and mania as well as a wide range of other psychiatric adverse drug reactions often related to overstimulation, such as insomnia, anxiety, agitation, emotional instability, and akathisia. They can also cause apathy and emotional indifference. There is also strong evidence that they cause lasting abnormalities in brain function and even brain anatomy, including abnormal brain cell proliferation, death of brain cells, and shrinkage of brain tissue. [Pg.191]

T No A No A PKA t PKC Brain, lung, skeletal muscle Synaptic plasticity, arrest of cell proliferation... [Pg.31]

U (No CaM) < O Q. CL Heart, kidney, Brain, liver, widespread Cardiac function, Ca2+-dependent regulation, hormonal regulation of gluconeogenesis, cell proliferation, coincidence detector for NO... [Pg.31]

Although mast cells and basophils probably account for >90% of stored histamine in the body, histamine is also present in platelets, enterochromaffin-like cells, endothelial cells, and neurons. Histamine can act as a neurotransmitter in the brain. Histaminergic nerves have their cell bodies within a very small area of the brain (the magnocellular nuclei of the posterior hypothalamus) but have axons in most areas of the forebrain. There is also evidence for axons projecting into the spinal (Fig. 1) cord. Finally, there is evidence that histamine synthesis can be induced in tissues undergoing rapid tissue growth and repair. In certain neonatal tissues (e.g. liver), the rate of synthesis of this unstored diffusable histamine (termed nascent histamine) is profound and may point to a role for histamine is cell proliferation. [Pg.588]

CXCL12 Stimulates Brain Tumor Cell Proliferation and Survival... [Pg.258]

Edgar We have looked at proliferating neuroblasts in the brain. When we coculture the brain with fat body those cells proliferate, but when we express activated ras in them without fat body, they don t proliferate. [Pg.196]

The sympathetic nervous system (SNS) and the hypothalamic-pituitary axis work together as important modulators of the immune system after exposure to stressors. Norepinephrine (NE) and epinephrine (EPI) (catecholamines from the SNS) and neuroendocrine hormones modulate a range of immune cell activities, including cell proliferation, cytokine and antibody production, lytic activity, and migration. This chapter will focus on these two major pathways of brain-immune signaling, briefly summarizing the evidence for SNS and hypothalamic-pituitary-adrenal (HPA) modulation of immune function, their influence on immune-mediated diseases, immune modulation in aging, and early life influences on these pathways. [Pg.490]

The toxicity of C60 has been found to be related to its ability to cause oxidative stress (Oberdorster, 2004 and Sayes et al., 2005, 2007). However, literature describing the toxicity of C60 is contradictoiy. The first report on C60 cytotoxicity originated from Tsuchiya et al. who found that C60 inhibited cell proliferation and differentiation dose-dependently in mouse midbrain cells treated at -400 pg/ml for six days. Tsuchiya et al. proposed that reactive oxygen species (ROS) contributed to C60 cytotoxicity. The ROS generation and embryo head abnormalities suggested that C60 may contribute to brain and neuronal diseases such as Down syndrome, Alzheimer s, and Parkinson s disease (Tsuchaiya, 1996). The research that... [Pg.268]

Investigations into die expression of distinct PKC isoenzymes in various tissues revealed a highly variable tissue distribution. PKCa and PKCX are ubiquitously expressed. Brain contains all isoenzymes, whereas others such as skin and skeletal muscle contain only a few (Blobe et al., 1994). Such a different pattern of expression suggests Aat the PKC isoenzymes play different roles in the tissue of expression and do not suggest a general role of all isoenzymes in cell proliferation. In many publications an influence of PKC on cell proliferation has been reported. [Pg.7]

Biological issues (i) Mg bioavailabihty, metabolism and physiology . (ii) Cell proliferation and differentiation , (iii) Animal husbandry. (iv) Magnesium in blood . (v) Genetic regulation , (vi) Mineral phase composition of bone and teeth . (vii) Brain and nervous system , (viii) Renal handling of magnesium . [Pg.268]

To study the functional implication of such observations, Santarelli et al. (2003) aimed at determining if an increase in neurogenesis is required for the effect of antidepressants. X-ray irradiation of the hippocampal area in adult rats causes long-term reduction in cell proliferation in the DG (Tada et al., 2000). Hippocampal x-ray irradiation, but not irradiation of other brain areas - like the SVZ or the cerebellar region - prevented the neurogenic effect... [Pg.12]


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See also in sourсe #XX -- [ Pg.214 ]




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