Effects of cigarette smoking on EEG spectral-band power, dimensional complexity, and nonlinearity during reaction-time task performance

Electroencephalogram (EEG) and heart rate (HR) were recorded while individuals performed visual and auditory go/no-go reaction time (RT) tasks. Overnight-abstaining smokers smoked two types of cigarettes in a single morning session. The first type was smoked once and had a nicotine yield of 0.05 mg. Two cigarettes of the second type (1.1 mg) were smoked. Four recordings were made: presmoking, postsmoking 0.05 mg, and postsmoking each 1.1 mg. HR was increased only by the first 1.1-mg cigarette. Smoking both the 1.1-mg cigarettes decreased RT. Smoking the first 1.1-mg cigarette increased EEG power in the beta2 band. A flexible effect of smoking the first 1.1-mg cigarette on EEG dimensional complexity (DCx) was obtained at locus Cz. Specifically, DCx was (a) raised when the presmoking level was low, (b) not affected when the presmoking level was intermediate, and (c) lowered when the presmoking level was high. Surrogate-data testing indicated the presence of nonlinearity in the EEG data that was not affected by smoking. Decreased RT was associated with increased DCx in the visual task only.     

POXVIRUS INFECTION AND APOPTOSIS

The following excellent reviews have been published on poxviruses and apoptosis during the last few years: P.C. Turner and R.W. Moyer, Semin. Virology, 8: 453–469, 1998; J.L. Shisler and B. Moss, Semin. Immunol., 13: 67–72, 2001; and H. Everett and G. McFadden, Curr. Opin. Microbiol., 5: 395–402, 2002. These articles dealt with the viral products and the mechanisms by which they interfere with apoptosis. In this review, we summarize new and old information and also introduce a new approach to explore interactions between the host cell and the replicating virus.     

Posttesticular development of spermatozoa of the tammar wallaby (Macropus eugenii)

Tammar wallaby spermatozoa undergo maturation during transit through the epididymis. This maturation differs from that seen in eutherian mammals because in addition to biochemical and functional maturation there are also major changes in morphology, in particular formation of the condensed acrosome and reorientation of the sperm head and tail. Of spermatozoa released from the testes, 83% had a large immature acrosome. By the time spermatozoa reached the proximal cauda epididymis 100% of sperm had condensed acrosomes. Similarly 86% of testicular spermatozoa had immature thumb tack or T shape head-tail orientation while only 2% retained this immature morphology in the corpus epididymis. This maturation is very similar to that reported for the common brush tail possum, Trichosurus vulpecula. However, morphological maturation occurred earlier in epididymal transit in the tammar wallaby. By the time spermatozoa had reached the proximal cauda epididymis no spermatozoa had an immature acrosome and thumbtack orientation. Associated with acrosomal maturation was an increase in acrosomal thiols and the formation of disulphides which presumably account for the unusual stability of the wallaby sperm acrosome. The development of motility and progressive motility of tammar wallaby spermatozoa is similar to that of other marsupials and eutherian mammals. Spermatozoa are immotile in the testes and the percentage of motile spermatozoa and the strength of their motility increases during epididymal transit. During passage through the caput and corpus epididymis, spermatozoa first became weakly motile in the proximal caput and then increasingly progressively motile through the corpus epididymis. Tammar wallaby spermatozoa collected from the proximal cauda epididymis had motility not different from ejaculated spermatozoa. Ultrastructural studies indicated that acrosomal condensation involved a complex infolding of the immature acrosome. At spermiation the acrosome of tammar wallaby spermatozoa was a relatively large flat or concave disc which projected laterally and anteriorly beyond the limits of the nucleus. During transit of the epididymal caput and proximal corpus the lateral projections folded inwards to form a cup like structure the sides of which eventually met and fused. The cavity produced by this fusion was lost as the acrosome condensed to its mature form as a small button-like structure contained within the depression on the anterior end of the nucleus. During this process the dorsal surface of the immature acrosome and its outer acrosomal membrane and overlying plasma membrane were engulfed into the acrosomal matrix. This means that the dorsal surface of the acrosomal region of the testicular tammar wallaby sperm head is a transient structure. The dorsal acrosomal surface of the mature spermatozoon appears ultrastructurally to be the relocated ventral surface of the acrosomal projections which previously extended out beyond the acrosomal depression on the dorsal surface of the nucleus of the immature spermatozoon.     

REM sleep eye movement counts correlate with visual imagery in dreaming: A pilot study

Based on the findings of our previously published positron emission tomography study, we proposed that recorded eye movements during REM sleep are visually targeted saccades. In the present study, we examined the correlation between the number of eye movements in REM sleep (EM) and visual imagery in dreaming (V) and provided further support for our proposal. All the observations (N= 11) were made with one individual to eliminate interindividual variation and were made during the second REM sleep period to control for a time-of-night effect. V, with or without dream report length partialled out, was strongly associated with EM only in the 1-min interval immediately preceding awakening. The time course of the association suggests that the strong EM–V association reflects a phasic, localized activation of the eye-movement-control system in association with REM sleep eye movements.     

THREE-DIMENSIONAL RECONSTRUCTION OF NON-HODGKIN'S LYMPHOMA IN BONE MARROW TREPHINES

The objective of this study was to analyse the location in the bone marrow of deposits of low-grade non-Hodgkin's lymphoma. This was achieved using computer-generated three-dimensional reconstruction techniques applied to serial tissue sections of five bone marrow trephines involved by lymphoma. For comparative purposes, previously published three-dimensional models of benign lymphoid aggregates in the bone marrow were used. The images generated by this new study showed that deposits of low-grade non-Hodgkin's lymphoma involving the bone marrow always assumed a paratrabecular pattern of infiltration at some point. This is in direct contrast to the pattern of bone marrow infiltration shown by benign lymphoid aggregates. It is concluded that location within the marrow space is a crucial factor in distinguishing between benign and low-grade malignant lymphoid infiltrates in the bone marrow. © 1997 by John Wiley & Sons, Ltd.     

Differential effects of waking from non-rapid eye movement versus rapid eye movement sleep on cardiovascular activity

The occurrence of cardiovascular events increases in the morning, and while the mechanism responsible is yet to be determined, possible contributors include surges in sympathetic activity and concurrent rises in blood pressure (BP). This study tested the hypothesis that the increase in sympathetic dominance and the surge in BP were greater when waking spontaneously from Stage 2 sleep compared with waking from rapid eye movement (REM) sleep. Twenty healthy young adults had overnight polysomnography, including electrocardiogram measurements. Spectral analysis of heart rate variability (HRV) was conducted on 2-min blocks of stable data selected from the last 30 min of sleep and during 30 min of resting wakefulness (supine) immediately following sleep. Outputs included absolute low frequency (LF) and high frequency (HF) power, the LF/HF ratio, heart rate (HR) and BP. To investigate the effect of waking from Stage 2 or REM sleep on HRV and BP responses, two-way analyses of variance ( anova s) (Stage 2 versus REM) with repeated measures (sleep versus morning wakefulness) were performed. It was found that waking from Stage 2 sleep was associated with significant increases in HR ( P  = 0·002) and BP ( P  < 0·001), as well as a tendency towards an increase in the LF/HF ratio ( P  = 0·08), whereas measurements during REM sleep and subsequent wakefulness were similar ( P  > 0·05). The greater increase in BP and HR when waking from Stage 2 sleep compared with REM sleep suggests that in vulnerable populations, waking from Stage 2 sleep could be an adjunct risk factor of cardiovascular events during the morning period.     

Binding of Acrylonitrile to Parvalbumin

A previous study has shown that acrylonitrile (ACN) has a longhalf-life in rainbow trout muscle and that [¹⁴C]ACN appearsto be bound to a 10,000-Da protein in muscle. The labeled proteinwas purified from muscle of trout exposed to [¹⁴C]ACN, separatedon 20% SDS–PAGE, and digested for amino acid analysisand sequence analysis. These studies indicated that the labeledprotein was the Ca2⁺-binding protein parvalbumin. Parvalbuminis an important calcium-binding protein thought to be involvedin the regulation of calcium levels in various parts of thebody ranging from neurons to fast-twitch muscle contractions.To study the reaction between parvalbumin and [¹⁴C]ACN, frogparvalbumin was incubated with [¹⁴C]ACN in vitro under variousconditions. These studies indicated that the maximum labelingoccurred at 1 nmol/nmol parvalbumin and at pH 7. Amino acidanalysis of the labeled protein indicated that the labeled aminoacid was probably histidine, and endoproteinase Glu-C (V-8)digestion studies revealed that the ¹⁴C was in the 1–81amino acid segment of the protein, an area that contains twohistidines.     

Reproductive Toxicity Evaluation of Methylethyl Ketoxime by Gavage in CD Rats

Methylethyl ketoxime (CAS No. 96-29-7; MEKO; 2-butanone oxime),an antioxidant agent used in paints, resins, and adhesives,was tested for reproductive toxicity in a two-generation studywith CD (Sprague-Dawley) rats. Thirty-eight-week-old rats/sex/group(F0) were administered MEKO in water, by gavage, at 0, 10, 100,or 200 mg/kg/day (at a dosing volume of 2 ml/kg), 5 days/weekfor 10 weeks with vaginal cytology evaluation (VCE) of F0 femalesduring the last 3 weeks of the prebreed period. Animals weremated within groups for 3 weeks with dosing during mating, gestation,and lactation for 7 days/week. F0 parents and F1 weanlings,10/sex/dose, were necropsied (after a 2-week postwean VCE inF0 females) with hematologic evaluation (including methemoglobin)and histology of adult livers, spleens, and reproductive organs.F1 weanlings, 30/sex/dose, were dosed for 11 weeks and matedas described above. Because of poor reproductive performance,not treatment related, F1 animals with no F2a litters were rebredto produce F2b litters. F1 parents and F2a weanlings, 10/sex/dose,were necropsied and evaluated as described above. Inguinal mammaryglands were examined histologically from all nonselected F1and F2 (a and b) female weanlings. Adult toxicity was observedin both generations and both sexes at all doses. Treatment-relatedparental deaths occurred at 200 mg/kg/day. At 100 and 200 mg/kg/day,parents exhibited dose-related reduced body weights and weightgains, reduced feed consumption, clinical signs of toxicity,and anemia with concomitant extramedul-lary hematopoiesis andhemosiderosis in livers and spleens (and increased spleen weights).At 10 mg/kg/day, only adult liver and spleen histologic effectswere present. There was no evidence of reproductive organ ormammary gland pathology or of reproductive or postnatal toxicityat any dose tested. There was no adult "no observable adverseeffect level" (NOAEL) established; the NOAEL for reproductiveand postnatal toxicity was at least 200 mg/kg/day for rats inthis study.     

CONTINUOUS EXTRADURAL ANALGESIA: COMPARISON OF MIDWIFE TOP-UPS, CONTINUOUS INFUSIONS AND PATIENT CONTROLLED ADMINISTRATION

We have compared three techniques used to provide extraduralanalgesia during the first stage of labour: 0.25% plain bupivacaine10ml demand top-ups delivered by the midwife; continuous infusionof 0.125% plain bupivacaine 10 ml h^–1 and patient-controlledextradural analgesia (PCEA) delivering 3-ml boluses of 0.25%bupivacaine. Each technique produced comparable analgesia achievingequivalent maternal satisfaction, with no difference in modeof delivery and no complications. This regimen for PCEA proveda viable alternative for continuous extradural analgesia andwas popular with the mothers, midwives and anaesthetists. ^*Present address: Department of Anaesthesia, Victoria Infirmary,Langside, Glasgow