Transient changes in inflammatory and oxidative stress markers with total sleep deprivation

Sleep and Biological Rhythms - Sleep deprivation (SD) is known to modulate inflammatory and oxidative stress markers. How these markers change over the SD period have seldom been studied in healthy...     

Mendelian hypertension with brachydactyly as a molecular genetic lesson in regulatory physiology

Mendelian forms of hypertension have delivered a treasure trove of novel genes. To date, the molecular mechanisms of five such syndromes have been largely clarified, including glucocorticoid-remediable aldosteronism, Liddle's syndrome, apparent mineralocorticoid excess, an activating mutation of the mineralocorticoid receptor, and pseudohypoaldosteronism type 2. Each of these conditions features salt sensitivity with increased sodium and volume reabsorption by the kidney and low plasma renin activity. None of the gene loci for these syndromes has been convincingly linked to hypertension in the general population. We are investigating kindreds who have autosomal-dominant hypertension and brachydactyly. Affected persons invariably have both anomalies. The hypertension is severe and results in death at about age 50 years from stroke. The condition resembles essential hypertension, because renin, aldosterone, and norepinephrine responses are normal and no salt sensitivity is present. The response to antihypertensive drugs is general. Another feature is diminished baroreflex sensitivity with markedly impaired blood pressure buffering. Furthermore, the ventrolateral medulla may be compromised in these patients, because neurovascular anomalies are a regular finding. We mapped the gene(s) for this disease to chromosome 12p and narrowed the chromosomal region by studying more affected families. Interestingly, the same locus was recently mapped in Chinese families with essential hypertension. Our 3-centimorgan region contains genes encoding a phosphodiesterase, an ATP-dependent potassium channel, and its regulator the sulfonylurea receptor 2. Screening of the coding regions revealed that none of these candidate genes harbor obvious mutations; however, other genetic mechanisms may nevertheless compromise their function. Our study underscores the importance of regulatory physiology to the understanding of a complex genetic syndrome.     

Tolerance, optimum ranges, and ecological requirements of freshwater Ostracoda (Crustacea) in Lake Aladağ (Bolu, Turkey)

During monthly sampling from Lake Alada (Bolu, Turkey) between April 2003 and June 2004, nine ostracod taxa (Candona candida, Cypridopsis vidua, Darwinula stevensoni, Eucypris virens, Eucypris sp., Heterocypris sp., Limnocythere inopinata, Physocypria kraepelini, and Tonnacypris lutaria) were recorded from seven stations. Physocypria kraepelini was commonly found in the lake while the others were recorded in particular months. UPGMA analyses clustered three groups based on their occurrence. Accordingly, the occurrence of species (C. candida, E. virens, and T. lutaria) was positive and significantly related to each other. Two species, P. kraepelini and D. stevensoni, showed a significant positive relationship with electrical conductivity. A significant negative correlation was found between the occurrence of P. kraepelini and dissolved oxygen, while there was a significant positive correlation between the occurrence of P. kraepelini and turbidity. About 76% of the relationship between species and environmental factors was explained by the first two axes of canonical correspondence analyses (CCA). Temperature and dissolved oxygen were the two most important influences on the species assemblages. All species showed different but high optima and tolerance ranges, corresponding with their cosmopolitan characteristics. These responses may be related to unstable ecological characteristics of Lake Alada, which is often subjected to human activity.     

The Protective Effect of Dexanabinol (HU-211) on Nitric Oxide and Cysteine Protease-Mediated Neuronal Death in Focal Cerebral Ischemia

We hypothesized that dexanabinol can prevent neuronal death by protecting neuronal lysosomes from nitric oxide (NO)-mediated toxicity, and in turn, by suppressing the release of cathepsins during cerebral ischemia. Focal cerebral ischemia was induced in two sets of animals by permanent middle cerebral artery occlusion. The first set was used to monitor NO concentration and cathepsin activity, while the second was used for histological examination with hematoxylin and eosin, and TUNEL staining. In post-ischemic brain tissue, NO content and cathepsin B and L activity increased (p < 0.05). Dexanabinol treatment reduced NO concentration and cathepsin activity to the control level (p > 0.05). The number of eosinophilic and apoptotic neurons increased in the post-ischemic cerebral cortex (p < 0.05). However, dexanabinol treatment lowered both of these (p < 0.05). We conclude that dexanabinol might be a useful agent for the treatment of stroke patients.