7 research outputs found
ÎČâCaryophyllene, the major constituent of copaiba oil, reduces systemic inflammation and oxidative stress in arthritic rats
A comprehensive, mechanistically detailed, and executable model of the cell division cycle in Saccharomyces cerevisiae
Healthy Eating: Approaching the Selection, Preparation, and Consumption of Healthy Food as Choice Behavior
Serotonin transporter availability in adults with autismâa positron emission tomography study
War: Back to the Future
Annual Review of Anthropology, 1999.War is a fraught subject. Those who study it often fight about it. This chapter examines the current state of the study of war, described and analyzed by anthropologists and nonanthropologists who employ concepts like culture in writing about the future of war. Warfare seems bound to keep us revisiting certain aspects of the past. At the same time, nothing induces change quite like conflict. Does war have a future? The preponderance of evidence-biological, archeological, ethnological- suggests that it does. But not all anthropologists agree. This in and of itself represents one of a series of gaps that begs further consideration
Molecular imaging of depressive disorders
This chapter summarizes findings of a large number of molecular imaging studies in the field of unipolar and bipolar depression (BD). Brain metabolism in depressed unipolar and bipolar patients is generally hypoactive in the middle frontal gyri, the pregenual and posterior anterior cingulate, the superior temporal gyrus, the insula, and the cerebellum, while hyperactivity exists in subcortical (caudate nucleus, thalamus), limbic (amygdala, anterior hippocampus), and medial and inferior frontal regions. Interestingly, after depletion of serotonin or noradrenalin/dopamine in vulnerable (recovered) major depressive disorder (MDD) patients, a similar response pattern in metabolism occurs. Findings on the pre-and postsynaptic dopaminergic system show indications that, at least in subgroups of retarded MDD patients, presynaptic dopaminergic markers may be decreased, while postsynaptic markers may be increased. The findings regarding serotonin synthesis, pre-and postsynaptic imaging can be integrated to a presumable loss of serotonin in MDD, while this remains unclear in BD. This reduction of serotonin and dopamine in MDD was recently summarized in a revised version of the monoamine hypothesis, which focuses more on a dysfunction at the level of the MAO enzyme. This should be addressed further in future studies. Nevertheless, it should be acknowledged that the serotonergic and dopaminergic systems appear adaptive; therefore, it remains difficult to distinguish state and trait abnormalities. Therefore, future longitudinal molecular imaging studies in the same subjects at different clinical mood states (preferably with different tracers and imaging modalities) are needed to clarify whether the observed changes in transporters and receptors are compensatory reactions or reflect different, potentially causal mechanisms. Several suggestions for future developments are also provided at the end of this chapter