Effects of bromocriptine and alpha-flupenthixol on sleep in REM sleep deprived rats.

Administration of bromocriptine mesylate (5 mg/kg, i.p.), a dopamine receptor stimulant, to rats which were deprived of REM sleep for 24 hours resulted in a significant increase in wakefulness as well as significant reduction of REM sleep during the first 5 hours of EEG recording. These effects were completely abolished by pretreatment with α-flupenthixol (0.2 mg/kg, i.p.), a dopamine receptor blocker. The loss of REM sleep has not been regained during the next 25 hours of EEG recording suggesting that the stimulation of dopamine receptors reduced REM sleep without causing subsequent REM rebound. These data raise questions on the negative dopamine control of REM sleep and on the potential use of dopamine stimulants in clinical situations characterized by excessive REM or by REM sleep dysfunction (narcolepsy).     

Arousal mechanisms: speedy flies don't sleep at night

Alertness and behavioral performance depend on an animal's level of arousal. In vertebrates, reinforcement and maintenance of arousal in the cortex are ensured by diffuse inputs from neurons releasing biogenic amine neuromodulators. Fruit flies similarly use dopamine for arousal control, indicating an ancient evolutionary origin of this essential feature of the functioning brain.     

Effects of dihydroergotoxine methane sulphonate (Redergine) on sleep in cats deprived of paradoxical sleep

Dihydroergotoxine methane sulphonate (DHET 1.0 mg/kg i.p.) was administered to cats deprived of paradoxical sleep (PS) for 72 h and 23 h of recovery sleep were recorded. During the first 12 h of recovery sleep slow-wave sleep (SWS) was significantly increased. There were no significant changes in the amounts of wakefulness (W), PS and several sleep indices. Analysis of the entire 23 h of recording period revealed no significant changes in any of the parameters studied. The results suggest that DHET has SWS enhancing property in the condition where "pressure" for PS was increased.     

Haploinsufficiency for tumour suppressor genes: when you don't need to go all the way

Classical tumour suppressor genes are thought to require mutation or loss of both alleles to facilitate tumour progression. However, it has become clear over the last few years that for some genes, haploinsufficiency, which is loss of only one allele, may contribute to carcinogenesis. These effects can either be directly attributable to the reduction in gene dosage or may act in concert with other oncogenic or haploinsufficient events. Here we describe the genes that undergo this phenomenon and discuss possible mechanisms that allow haploinsufficiency to display a phenotype and facilitate the pathogenesis of cancer.     

Nucleic acid and protein content of cells of the raphe nuclei of the rat brain when the animals are deprived of the paradoxical sleep phase

A 24 hours paradoxical sleep deprivation (PSD) with rats resulted in lowering the RNA content in neurons and gliocytes of n. raphé dorsalis by 31 and 18%, resp.; the protein content remaining unchanged. A 48 hours PSD reduced RNA and protein contents in neurons by 31%; in gliocytes both these substances being on the control level. In the neurons of n. raphé pontis, by the end of the 1st day of PSD the contents of both RNA and protein were seen reduced by 16 and 28%, resp.; however, by the end of the 2nd day their levels well compared with those in the control rats. There was a phase oscillation of protein content in gliocytes: from - 19%, on the first day of PSD, to +19%, on the 2nd day. There is a great resemblance in response to PSD between the adrenergic nucleus - locus coeruleus - and n. raphé pontis, whereas their responses differ from that of the serotoninergic n. raphé dorsalis.     

Prior sleep and perceptions of risk when driving

Fatigue represents a significant driving risk. One predictor of fatigue, and driving impairment, is prior sleep length. However, it is currently unknown how much sleep driver’s perceive as necessary to drive safety. This may be an important contributor to a driver’s decision about whether they are safe to drive. There is also evidence that reduced prior sleep leads to increased risk-taking. The aim of this study was to investigate community perceptions regarding sleep duration and fatigued driving, and to determine if sleep duration influences risk perception in relation to fatigued driving. 1081 participants completed a telephone survey addressing sleep history, fatigued driving, and risk perception. The majority of the sample (62.4 %) thought a minimum of 6–8 h sleep was necessary to drive safely, however a small percentage (5.6 %) felt that less was necessary or reported that they did not know. Women tended to report that individuals need more hours of sleep to drive safely. Younger age and male gender were both associated with an increased likelihood of reporting having driven despite feeling too tired, and male gender alone with being more likely to report falling asleep at the wheel. Reduced sleep duration in the prior 48 h was associated with reports of driving when too tired, and the perception that less sleep was required to drive safely. These findings imply that the Australian public may need guidance about sleep and safe driving, particularly in regards to the potential for sleep to influence risk propensity.

     

Sorption of sulfophthaleinic dyes by the brain synaptosomes of rats deprived of parodoxical sleep

The influence of paradoxical sleep deprivation on sorption of bromphenol blue, bromcresol green and bromthymol blue by rat's brain synaptosomes was studied. Effect of sleep disturbance (increase in the number of dye bindings) was shown to augment with the increase in hydrophobicity of the sulfophtaleinic dye.     

Psychiatry-epitomes of progress: stimulants and hyperkinesis

Although used around the world since 1949, lithium has come into extensive use in psychiatry in the United States only within the past decade. Before initiating treatment with this drug, physicians must be familiar with the diagnostic scheme of the major affective disorders, the indications and contraindications to lithium''s use, and its principles of treatment, including evaluation before lithium therapy, criteria for monitoring blood levels and signs of impending toxicity.Despite earlier reports about the toxicity of lithium when it was promoted as a salt substitute, lithium is a safe drug. Its use not only has revolutionized the treatment of the major affective disorders, but has opened up new and broad avenues of research into the regulation of man''s emotions.     

Life-history evolution in uncertain environments: bet hedging in time

Many vertebrates, forest herbs, and trees exhibit both variable age at maturity and iteroparity as adaptations to uncertain environments. We analyze a stochastic model that combines these two life-history adaptations with density-dependent fertility. Results for a model with only iteroparity are consistent with previous work; environmental uncertainty favors adult survival over juvenile survival. This holds true even if there is a moderately strong convex trade-off between adult survival and fecundity, but the direction of selection can depend on which life-history trait is considered a random variable. A life history with only developmental delay favors juvenile survival in uncertain environments, consistent with previous models of seed banks. When both developmental delay and iteroparity are included in the model, both adaptations are favored in uncertain environments. Our simulations show that selection is not necessarily a runaway process in which either developmental delay or iteroparity is favored, as recently proposed by Tuljapurkar and Wiener, but rather that selection can favor both mechanisms. Invasion analysis shows that selective pressure on life-history delays increases as environmental variation increases. Reproductive delay and adult survival can be either adaptations or constraints. Natural-history studies that estimate model parameters can resolve this uncertainty.     

Structural-functional and metabolic changes in the nervous system in low- and high-excitable rats deprived of paradoxical sleep

Studying of the influence of 24-hour deprivation of paradoxical sleep phase (PSPh) on rats with different genetically determined levels of excitability of the nervous system allowed to establish: 1) significant changes in functional state of the central part of the nervous system responsible for elaboration and preservation of defensive conditioned reflexes; 2) considerable lowering of functional state of the peripheral nervous system expressed both in a decrease of tibial nerve excitability thresholds and in changing of morpho-tinctorial characteristics of the studied nerve receptor parameters. The degree of the observed effects of PSPh deprivation is dependent on animal line belonging.