Small Physiological Changes Research Articles

The Absence of (p)ppGpp Renders Initiation of Escherichia coli Chromosomal DNA Synthesis Independent of Growth Rates.

The initiation of Escherichia coli chromosomal DNA replication starts with the oligomerization of the DnaA protein at repeat sequences within the origin (ori) region. The amount of ori DNA per cell directly correlates with the growth rate. During fast growth, the cell generation time is shorter than the time required for complete DNA replication; therefore, overlapping rounds of chromosome replication are required. Under these circumstances, the ori region DNA abundance exceeds the DNA abundance in the termination (ter) region. Here, high ori/ter ratios are found to persist in (p)ppGpp-deficient [(p)ppGpp0] cells over a wide range of balanced exponential growth rates determined by medium composition. Evidently, (p)ppGpp is necessary to maintain the usual correlation of slow DNA replication initiation with a low growth rate. Conversely, ori/ter ratios are lowered when cell growth is slowed by incrementally increasing even low constitutive basal levels of (p)ppGpp without stress, as if (p)ppGpp alone is sufficient for this response. There are several previous reports of (p)ppGpp inhibition of chromosomal DNA synthesis initiation that occurs with very high levels of (p)ppGpp that stop growth, as during the stringent starvation response or during serine hydroxamate treatment. This work suggests that low physiological levels of (p)ppGpp have significant functions in growing cells without stress through a mechanism involving negative supercoiling, which is likely mediated by (p)ppGpp regulation of DNA gyrase.IMPORTANCE Bacterial cells regulate their own chromosomal DNA synthesis and cell division depending on the growth conditions, producing more DNA when growing in nutritionally rich media than in poor media (i.e., human gut versus water reservoir). The accumulation of the nucleotide analog (p)ppGpp is usually viewed as serving to warn cells of impending peril due to otherwise lethal sources of stress, which stops growth and inhibits DNA, RNA, and protein synthesis. This work importantly finds that small physiological changes in (p)ppGpp basal levels associated with slow balanced exponential growth incrementally inhibit the intricate process of initiation of chromosomal DNA synthesis. Without (p)ppGpp, initiations mimic the high rates present during fast growth. Here, we report that the effect of (p)ppGpp may be due to the regulation of the expression of gyrase, an important enzyme for the replication of DNA that is a current target of several antibiotics.

Microfluidic Single-Cell Analytics.

What is the impact of cellular heterogeneity on process performance? How do individual cells contribute to averaged process productivity? Single-cell analysis is a key technology for answering such key questions of biotechnology, beyond bulky measurements with populations. The analysis of cellular individuality, its origins, and the dependency of process performance on cellular heterogeneity has tremendous potential for optimizing biotechnological processes in terms of metabolic, reaction, and process engineering. Microfluidics offer unmatched environmental control of the cellular environment and allow massively parallelized cultivation of single cells. However, the analytical accessibility to a cell's physiology is of crucial importance for obtaining the desired information on the single-cell production phenotype. Highly sensitive analytics are required to detect and quantify the minute amounts of target analytes and small physiological changes in a single cell. For their application to biotechnological questions, single-cell analytics must evolve toward the measurement of kinetics and specific rates of the smallest catalytic unit, the single cell. In this chapter, we focus on an introduction to the latest single-cell analytics and their application for obtaining physiological parameters in a biotechnological context from single cells. We present and discuss recent advancements in single-cell analytics that enable the analysis of cell-specific growth, uptake, and production kinetics, as well as the gene expression and regulatory mechanisms at a single-cell level.

Stimuli-Responsive Polysaccharide Hydrogels for Biomedical Applications: a Review

This review aims to present methods for obtaining polysaccharide hydrogels, their properties and sensitivity to environmental stimuli, as well as their potential applications in biomedicine. Living systems respond to external stimuli by adapting themselves to changing conditions. Hydrogels are a class of materials with 3D networks of polymers that can absorb high amounts of water or biological fluids while remaining insoluble under physiological conditions compared with general absorbent materials, with their characteristic being dependent on network structure and the external environment. Stimuli-responsive hydrogels have the ability to respond to changes in their external environment. They can exhibit dramatic changes in their swelling behavior, network structure, permeability, and mechanical strength in response to variations in temperature, pH, glucose, electric field, light, etc. However, such changes are reversible; therefore, hydrogels can convert to their initial state as soon as the trigger is removed. Because of compatibility with living tissues, hydrogels can be used in different biomedical purposes. The application of stimuli-responsive polysaccharide hydrogels in the biomedical field has become increasingly popular with many research groups and industries. In addition to their ability to undergo large reversible transitions in their swelling behavior due to small physiological or environmental changes, they are also often highly biocompatible and versatile and possess a high storage capacity for the immobilization of biomolecules.

Evaluation of Neurotherapy Program for a Patient with Clinical Symptoms of Schizophrenia and Severe TBI Using Event-related Potentials

Background Despite recent interest in the brain/mind problem and the possible organic correlates of mental disease, relatively few case studies have examined the problem concretely. I examined the effectiveness of neurotherapy for a 68-year-old male schizophrenic patient whose psychotic symptoms displayed qualitative and quantitative changes after a closed-head injury. It was hypothesized that there would be good response to relative beta training applied to regulate the dynamics of brain function. Case description The patient was diagnosed with schizophrenia in the early 1960s and frequently thereafter hospitalized. Visual hallucinations were the dominant symptom, and art therapy provided some relief, which led to a successful artistic career. In 1989, while actively hallucinating, he suffered a mild TBI in a pedestrian accident, an in consequences, he presented with perseveration, hemispatial neglect, and disturbances of working memory. The patient took part in 20 sessions of relative beta training. Standardized neuropsychological testing and Event Related Potentials (ERPs) before and after the completion of the program were used. As hypothesized, there was marked improvement of neurophysiological, neuropsychological, and psychiatric symptoms, as well as executive dysfunction and behavioral disorders. He also began to paint in a completely different style. Conclusions The pathomechanisms of schizophrenia and neurobehavioral disturbances resulting from organic brain damage are not unrelated. Microgenetic theory can provide a basis for explaining the course of symptoms in this and similar cases. Relative beta training produced behavioral changes and small physiological changes. ERPs can be used to assess functional brain changes induced by neurotherapeutic programs.

Ketogenic diet sensitizes glucose control of hippocampal excitability

A high-fat low-carbohydrate ketogenic diet (KD) is an effective treatment for refractory epilepsy, yet myriad metabolic effects in vivo have not been reconciled clearly with neuronal effects. A KD limits blood glucose and produces ketone bodies from β-oxidation of lipids. Studies have explored changes in ketone bodies and/or glucose in the effects of the KD, and glucose is increasingly implicated in neurological conditions. To examine the interaction between altered glucose and the neural effects of a KD, we fed rats and mice a KD and restricted glucose in vitro while examining the seizure-prone CA3 region of acute hippocampal slices. Slices from KD-fed animals were sensitive to small physiological changes in glucose, and showed reduced excitability and seizure propensity. Similar to clinical observations, reduced excitability depended on maintaining reduced glucose. Enhanced glucose sensitivity and reduced excitability were absent in slices obtained from KD-fed mice lacking adenosine A1 receptors (A1Rs); in slices from normal animals effects of the KD could be reversed with blockers of pannexin-1 channels, A1Rs, or KATP channels. Overall, these studies reveal that a KD sensitizes glucose-based regulation of excitability via purinergic mechanisms in the hippocampus and thus link key metabolic and direct neural effects of the KD.

Robust cardiac BOLD MRI using an fMRI‐like approach with repeated stress paradigms

Use repeated stress paradigms and an approach taken from neurological blood oxygen level dependent (BOLD) functional MRI (fMRI) to derive robust cardiac BOLD measurements. Multiple-repetition, single-shot, electrocardiograph-triggered, T2-prepared BOLD balanced steady-state free precession was performed during repeated long breath-holds in 13 volunteers. Nonrigid motion correction was applied to the continuously acquired data and it was analyzed with a general linear model (GLM) taking into account the effects of the breath-hold duration, RR interval, motion, and baseline variations. Both voxel- and region of interest-based analyses were performed. The GLM model was able to isolate the component of the BOLD signal arising from the breath-holds and separate it from the background effects due to the changing heart rate and motion. A significant (P<0.05) BOLD signal increase was observed in the myocardium of healthy volunteers. Using a recent elastic motion correction algorithm and adapted acquisition techniques, it was possible to apply fMRI-like strategies for cardiac BOLD MRI in volunteers and derive robust BOLD measurements. The observed slight but significant oxygenation increase in the myocardium of volunteers might be explained by the vasodilator effect of increased CO2 concentration under apnea. Detection of such small physiological changes in volunteers performing breath-holds demonstrates that the method could have potential in identifying low oxygenation regions in the myocardium of patients during stress tests.

Effect of percussion impulse sounds on hearing

Impulse-like sounds with high peak pressure levels emitted by percussion instruments often occur in music. The potentially harmful effect to the inner ear caused by these sounds is not fully understood. Solely the physical description of impulses like peak pressure level, etc. is not considered meaningful enough to assess their hazard. Therefore, the Auditory Hazard Assessment Algorithm for Humans (AHAAH), which is based on a physiological model, seems to be more appropriate. Another quantity to assess auditory hazard is the change of otoacoustic emissions (OAEs) after a sound exposure. It allows the individual detection of small physiological changes of the outer hair cells before any serious damages and threshold shifts may occur. In a pilot experiment the sounds of several percussion instruments have been measured at the players’ ears in a regular rehearsal situation. To assess the auditory hazard of the measured sounds the players’ OAEs have been measured before and after playing on the instruments. Despite peak levels of about 140 dB, the OAEs did not change significantly and the AHAAH rated nearly all sounds as harmless. It can be concluded that impulse sounds in music with high peak levels are not necessarily hazardous.

Spatio-temporal patterns of chlorophyll fluorescence and physiological and structural indices acquired from hyperspectral imagery as compared with carbon fluxes measured with eddy covariance

This study provides insight into the assessment of the spatio-temporal trends of chlorophyll fluorescence, narrow-band physiological indices, and structural indices acquired with a hyperspectral imager flown over a flux tower in a canopy characterized by small seasonal structural changes and a heterogeneous architecture. A total of seven flights between summer and autumn were conducted with a hyperspectral camera that captured 30cm resolution imagery and 260 spectral bands in the 400-900nm region. This enabled the identification of pure-vegetation tree crown pixels around an eddy covariance flux tower without shadow components or background effects. The hyperspectral imagery was used to study the temporal patterns of canopy fluorescence and reflectance indices related to physiology and canopy structure. The seasonal trends observed in the airborne indices and fluorescence and their relationship with gross primary production (GPP) demonstrated that vegetation indices mostly related to structure such as the normalized difference vegetation index (NDVI) and the enhanced vegetation index (EVI) yielded non-significant relationships (r2=0.17; p>0.05) due to the small structural changes in the canopy through the season. By contrast, physiological indices related to chlorophyll content (TCARI/OSAVI), light use efficiency (PRI570), and canopy chlorophyll fluorescence calculated through the Fraunhofer Line Depth principle (FLD3) showed a similar seasonal trend to that of GPP measured at the same time of the flights (r2 in the range 0.75–0.84; p<0.01). These results are consistent with the physiological trend observed during summer and autumn, which showed that chlorophyll content increased by 17.9% while the NDVI and the estimated tree crown projected LAI (LAIp) remained almost constant during the experiment (3% variation). The time-series hyperspectral dataset demonstrated that the seasonal trajectories of the NDVI and EVI were weakly related (p>0.05) to the physiological indicators such as TCARI/OSAVI, PRI570 and fluorescence. The spatial variability of the hyperspectral indices investigated through the coefficient of variation (CV) showed that fluorescence around the tower varied up to 17% at the time of the maximum stress (summer), while LAIp showed little variation during that time (CV=1.8%). After the summer stress period, the CV for fluorescence and chlorophyll content decreased in autumn down to 9%. This study demonstrates that small physiological changes occurring in an evergreen canopy were still captured by remote sensing physiological indices and high-resolution airborne fluorescence. These indicators are required for GPP monitoring when the vegetation dynamics are not captured by remote sensing structural indices.

The effects of different environmental conditions on thermoregulation and clinical and hematological variables in long-distance road-transported calves1

The aim of this study was to investigate the effects of long-distance road transport (19 h, from Poland to Italy) during 2 seasons (summer vs. winter) on clinical and hematological variables in calves. The environmental temperature range that could compromise the thermoregulation system (thermal stress) of the calves was tested. For the 7 Holstein calves in each transport, the BW and rectal temperature (RT) were measured, and blood samples were collected at the farm of origin, before loading at the transit center (T2), after unloading at the farm of destination (T3), and 1, 2, 3, and 4 d after arrival. The body temperature (BT) and heart rate (HR) were continuously monitored from T2 to T3. The data were statistically analyzed according to a mixed model that considered the fixed effects of transport (repeated measurements), season of journey, and their interaction. Within the observed temperature-humidity index (THI) range (30 to 80), effective thermoregulation allowed the calves to maintain their BT with small physiologic changes to prevent thermal stress, particularly in the summer. With no seasonal differences, the HR was greater at loading than unloading (120 vs. 115 beats per min; P = 0.012). As for the transport effect, the BW was less (P < 0.001) after unloading, and the RT was greater (P = 0.004). This effect was more marked in summer. The hematological variables indicated a moderate effect of transport on the hydration condition, reactive and muscular systems, and metabolism, although hematocrit (P = 0.004), erythrocytes, cortisol, NEFA, β-hydroxybutyrate, lactate, creatine kinase, lactate dehydrogenase, and aspartate aminotransferase activity (P < 0.001), and total protein (P = 0.007) were greater after unloading. This was confirmed by a moderate decrease in total leukocytes (P = 0.031) and glucose concentration (P = 0.002). The changes in the clinical variables were similar for both seasons even though in the summer, hematocrit (P < 0.001), urea (P = 0.008), and total protein (P = 0.010) increased and glucose concentration (P = 0.038) decreased. In conclusion, the data did not show a pronounced effect attributable to the season of the journey. Long-distance road transport leads to notable changes in clinical and hematological variables at the end of the journey. However, these variables remained within their physiological ranges and returned to basal values within a few days after the journey.

Reproducibility of the CMAP scan

IntroductionThe CMAP scan is a surface EMG method based on the successive activation of motor units. It provides information about reinnervation processes, the number of functional motor units and nerve excitability. The CMAP scan has potential value as a follow-up tool in monitoring disease progression, recovery or aging of the peripheral nerves. In this study, we assessed its interobserver and different-day reproducibility. MethodsTwo investigators recorded CMAP scans in ten healthy subjects, each on two different days. Intraclass correlation coefficients (ICCs) and coefficients of variation (CoVs) were calculated for the parameters extracted from the CMAP scan. ResultsAll CMAP scan parameters had a good different day (ICCs >0.8 and CoVs <15%) and interobserver reproducibility (ICCs >0.7 and CoVs ⩽15%). Different-day reproducibility was better than interobserver reproducibility. ConclusionCMAP scan test–retest variability is small, suggesting that as a follow-up tool it may be sensitive to fairly small (patho)physiological changes in the studied variables.

Gill morphometry and hematology of juvenile chinook salmon chronically exposed to treated (elemental chlorine-free) bleached kraft pulp mill effluent at low temperature to simulate winter exposure

We used an on-site mobile laboratory to assess the effects of pulp mill effluent on juvenile (~0.9 g) chinook salmon, Oncorhynchus tshawytscha (Walbaum in Artedi, 1792), that normally overwinter under ice in the upper Fraser River at Prince George, British Columbia. After a 28-day exposure at 0.4–2.7 °C to secondary-treated bleached kraft mill effluent (TBKME; 0%, 2%, 4%, 8%, or 16%) under both normoxic and hypoxic (~67% air saturation) conditions, hematocrit (Hct), leucocrit (Lct), and differential white blood cell counts were determined and gills were examined for gross and fine morphometry. TBKME had no effect on either Hct or Lct, but the highest TBKME concentration (16%) increased lymphocyte numbers, reduced secondary lamellae numbers, and increased the blood–water diffusion distance of secondary lamellae. Given the relatively high TBKME concentration, compared with actual discharges to the river, and the small physiological changes observed, it appears that chronic winter exposure of juvenile chinook salmon to TBKME under hypoxic winter conditions is unlikely to produce major disturbances to these aspects of the fish's physiology.

Small physiologic changes in calcium and magnesium alter excitability and burst firing of CA1 pyramidal cells in rat hippocampal slices.

The effects of small physiologic changes in Ca and Mg concentrations on neuronal burst firing were examined. Intracellular electrophysiologic recordings were made from CA1 pyramidal neurons in rat hippocampal slices. There was no difference in the resting potential or the input resistance of neurons bathed in the lower Ca-Mg artificial Cerebrospinal fluid (aCSF) (1.4 mM Ca; 1.3 mM Mg) compared with the higher Ca-Mg aCSF (2 mM Ca; 2 mM Mg). However, neurons in the lower Ca-Mg aCSF, but not the higher Ca-Mg aCSF, demonstrated depolarizing waves and bursts of action potentials; no single component of the aCSF accounted for this difference. Reducing the Ca from 2 to 1 mM in the higher Ca-Mg aCSF increased the mean frequency of action potentials from 28 to 171 Hz; the addition of 6-cyano-7-nitroquinoxaline-2,3-dione did not reduce the frequency. The threshold of potassium for inducing bursts was 5.25 with 1 mM Ca, 7.25 with 2 mM Ca, and 11.25 with 3 mM Ca. When Mg was reduced from 2 to 1 mM, the number of potassium-induced bursts increased to 190%; increasing Mg from 2 to 3 mM reduced the bursts to 58% (frequency with 2 mM Mg set to 100%). Small decreases in extracellular Ca and/or Mg led to increased excitability and burst firing, which may alter physiologic and pathophysiologic processes such as enhancing long-term potentiation, pain transmission, epileptogenesis, and neuronal damage and decreasing anesthetic potency. Increases in extracellular Ca and/or Mg would have the opposite effect on these processes. These effects of extracellular divalent ions on burst firing may explain some of the pathophysiologic effects of hypocalcemia and hypomagnesemia.

Changes in extracellular Ca2+ over a physiologic concentration range differentially modulate reactivity of resistance arteries of spontaneously hypertensive and normotensive rats.

Norepinephrine-induced contractile responses of mesenteric resistance arteries of normotensive Wistar Kyoto (WKY) and spontaneously hypertensive (SHR) rats were examined in the presence of 1.25, 1.5, and 2.5 mM extracellular Ca2+. In endothelium-intact WKY segments, the three levels of extracellular Ca2+ had no effect on sensitivity to norepinephrine. However, the response of SHR vessels to low dose norepinephrine was significantly enhanced in the presence of 1.25 and 2.5 mM Ca2+ versus 1.5 mM Ca2+. After endothelial WKY vessels responded like SHR vessels, i.e. sensitivity to norepinephrine was enhanced in 1.25 mM Ca2+ compared with 1.5 mM Ca2+. This response to alterations in extracellular Ca2+ was also observed after blockade of the neuronal amine pump with cocaine. These results indicate that vascular smooth muscle of both SHR and WKY respond to small physiologic changes in extracellular Ca2+ with altered sensitivity to norepinephrine. This effect is independent of the neuronal amine pump. We conclude that the endothelium of the normotensive rat protects against Ca(2+)-induced changes in sensitivity to norepinephrine and this protection is absent in SHR.

The tilapia prolactin cell: A model for stimulus-secretion coupling

The tilapia prolactin (PRL) cell responds rapidly (10-20 min) to small physiological changes in medium osmotic pressure (OP), releasing increasing quantities of hormone as medium OP is reduced. This release is rapidly (≤ 10 min) inhibited by somatostatin (SRIF). There is now extensive evidence that tilapia PRL cell function is regulated through the second messengers Ca(++) and cAMP. Our studies have shown that PRL release is augmented by treatments that lead to increased levels of intracellular Ca(++) or cAMP. On the other hand, PRL release is blocked when tissues are incubated in Ca(++)-depleted medium or upon the addition of Co(++), an inhibitor of Ca(++)-mediated processes. The use of(45)Ca(++) to characterize the movement of Ca(++) into PRL cells has provided evidence that an increase in the influx of extracellular Ca(++) may participate in PRL release upon exposure to hyposmotic medium. Our studies have also shown that SRIF suppresses the increase in(45)Ca(++) accumulation that is brought about when OP is reduced. We have also examined the effects of OP and SRIF on cAMP levels. The reduction of medium OP did not alter cAMP metabolism during 20 min of incubation. By contrast, cAMP accumulation in the presence of IBMX was enhanced at 1 hr of incubation in reduced OP. Thus, an increase in cAMP turnover may play a role in maintaining PRL release under sustained stimulation. SRIF reduced the accumulation of cAMP during 10 min of incubation with IBMX and also reduced the forskolin-stimulated increase in cAMP. Thus, SRIF may suppress adenylate cyclase activity. Finally, our studies have revealed that the forskolin-stimulated increase in cAMP levels is not dependent upon medium Ca(++). The presence of Ca(++) in the medium is required, however, for PRL release even when the cAMP messenger system has been activated. Moreover, cAMP accumulation was augmented when intracellular Ca(++) was increased. This raises the possibility that reduced OP may stimulate an increase in cAMP turnover indirectly through its action(s) on cytosolic Ca(++).

Unusual sensitivity of cytosolic free Ca2+ to changes in extracellular Ca2+ in rat C-cells.

An essential function of C-cells is to monitor extracellular Ca2+ concentration ([Ca2+]e) and to respond to changes in [Ca2+]e by regulating hormone secretion. Using the calcitonin-secreting rat C-cell line rMTC 44-2, we have investigated a possible tight linkage between [Ca2+]e and cytosolic free Ca2+ ([Ca/+]i). We have demonstrated, using the Ca2+ indicator Quin 2, that the [Ca2+]i is particularly sensitive to changes in [Ca2+]e. Sequential increases in [Ca2+]e as small as 0.1 mM evoke clear elevations in [Ca2+]i. In contrast, other cell types tested did not alter their [Ca2+]i in response to increasing [Ca2+]e even to levels as high as 4.0 mM. Sequential 1.0 mM increments in [Ca2+]e caused the [Ca2+]i to rise from a base line of 357 +/- 20 nM Ca2+i at 1.0 mM Ca2+e to a maximum of 1066 +/- 149 nM Ca2+i at 5.0 mM Ca2+e. [Ca2+]e above 2.0 mM produced a biphasic response in [Ca2+]i consisting of an immediate (less than 5 s) spike followed by a decay to a new plateau. Treatment of rMTC 44-2 cells with either 50 mM K+ or 100 nM ionomycin at 1.0 mM Ca2+e caused an immediate spike in [Ca2+]i to micromolar levels. Pretreatment with EGTA or verapamil inhibited completely the increase in [Ca2+]i induced by 50 mM K+. However, pretreatment with EGTA only slightly attenuated the spike phase in [Ca2+]i produced by ionomycin, demonstrating that ionomycin released intracellular stores of calcium. We conclude that rMTC 44-2 cells regulate [Ca2+]i by monitoring small physiological changes in [Ca2+]e, the primary secretagogue for C-cells.

An oscillating intratubular pressure response to alterations in Henle loop flow in the rat kidney.

We describe in gas anesthetized rats an oscillating intratubular pressure response, probably of vascular origin, sensitive to small physiological changes in fluid delivery to the distal tubule. The oscillation apparently indicates that an adjustment of vascular resistance is in operation, but at present it reveals neither the effector site (afferent and/or efferent arteriole) nor the effector mechanism (vasoconstriction and/or dilatation). The renin-angiotensin system seems to be involved in this phenomenon.

Effect of acute vasopressin infusion on blood pressure and plasma angiotensin II in normotensive and DOCA-salt hypertensive rats.

1. Arginine vasopressin was infused at 0.5, 2, 6, 18 or 54 ng min(-1) kg(-1) for 1 hr into normal, sham-operated and DOCA-salt hypertensive rats. Complete vasopressin/blood pressure dose-response curves were constructed from circulating plasma vasopressin concentrations measured at the end of each infusion. 2. DOCA-salt hypertensive rats had a higher basal plasma vasopressin concentration (11.1 +/- SD 3.7 fmol/ml) than either the normal (3.9 +/- 2.3, P less than 0.01) or the sham-operated rats (4.5 +/- 2.4, P less than 0.01). 3. The DOCA-salt hypertensive rats did not have my detectable enhancement of pressor sensitivity, compared with either of the two normotensive groups. 4. There was no significant increase in blood pressure in either the normal rats or sham-operated rats until vasopressin was infused at 2 ng min(-1) kg(1), when the plasma concentration was between 30 and 40 fmol/ml. 5. Subpressor infusion of vasopressin in the normal and sham-operated rats, which gave plasma concentrations of 22-23 fmol/ml, completely suppressed plasma angiotensin II to levels similar to the basal values found in the DOCA- salt hypertensive rats (10.5 +/- 2.3, 14.5 +/- 4.5 and 8.0 +/- 1.6 fmol/ml respectively). 6. These findings suggest that the mechanism of vasopressin involvement in DOCA-salt hypertension is as yet unclear, that short-term changes in vasopressin concentration appear unimportant in the regulation of normal blood pressure, that small physiological changes of vasopressin in normal rats may be important in the regulation of renin secretion, and that the increase in vasopressin concentration seen in DOCA-salt hypertension may contribute to the suppression of renin and angiotensin II in this state.

Effect of hemorrhage on fever: the putative role of vasopressin

The effects of hemorrhage on the febrile response of the sheep was examined because hemorrhage is a potent stimulant for arginine vasopressin (AVP) release into cerebrospinal fluid and blood. Removal of 20% of the estimated blood volume of the conscious sheep led to small physiologic changes and significantly decreased fevers in response to bacterial endotoxin. Mean arterial blood pressure decreased in hemorrhaged febrile sheep to a significantly greater extent than in nonhemorrhaged febrile sheep. AVP levels were considerably greater in the blood of hemorrhaged febrile sheep than in nonhemorrhaged febrile sheep and the concentrations correlated with the magnitude of the decrease in fever. Sheep hemorrhaged in the cold had changes in body temperature similar to control sheep. These experiments support the hypothesis that AVP may be an antipyretic neuromodulator.

Physiological and subjective effects of Zen meditation and demand characteristics.

Forty male undergraduate volunteers were assigned to one of four groups. During the treatment period, the control group was asked to “just sit there.” The deactivation demand, neutral demand, and activation demand groups were shown a videotape demonstrating the Zen meditation exercise “counting breaths” and modeling and suggesting relaxation outcome, no specific outcome, and arousal outcome for each group, respectively. A baseline period preceded and a recovery period followed treatment. Respiration rate and electromyogram decreased and heart rate increased, then gradually declined for the meditation groups during the treatment period. Differences among groups in self-reported mood were not statistically reliable. Results show that Zen meditation produces small physiological changes in naive, unpracticed subjects.