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At least 595 records · Page 33Linked to original sources
PubMed1984

Body temperature responses of aged mice to ambient temperature and humidity stress.

Male C57BL/6 mice aged 6 to 7 months, 13 to 14 months, and 19 to 20 months were acutely exposed to four ambient temperature (15 degrees C, 20 degrees C, 30 degrees C, 35 degrees C) and two relative humidity (50% rh, 80% rh) conditions. Three-hour average rectal temperatures were compared across age groups and environmental conditions. At the two temperature extremes of 15 degrees C and 35 degrees C, there was a very marked age-associated hypothermia and hyperthermia, respectively. This hypothermic response was maintained by the 19 to 20-month-old mice during exposure to 20 degrees C and thermoneutrality (30 degrees C). At any given ambient temperature, relative humidity had no effect on thermoregulatory function in the oldest mice, whereas the 6 to 7-month- and 13 to 14-month-old mice were sensitive to the effects of humidity at 15 degrees C and 20 degrees C.

Aging↗
PubMed2004

The X-ray crystallographic study of the conformation of Z-DNA which bound to polyamine for the minor groove at room temperature and low temperature.

We succeeded in x-ray crystal analysis of d(CG)3 with N1-{2-[(2-amino-ethylamino)-ethylamino]-ethyl}-ethane-1,2-diamine complex at three conditions (1: room temperature 2: low temperature 3: highly salt condition). At room temperature two polyamines took extended form and bound to minor groove of d(CG)3, at low temperature two polyamines took U-shape form and lied in minor groove of d(CG)3, at highly salt condition two polyamines took fishhook form and one polyamine lied in upper side of minor groove and the other polyamine lied in down side of minor groove of d(CG)3.

Crystallography, X-Ray↗
PubMed2000

Characterization of a mutant form of SecA that alleviates a SecY defect at low temperature and shows a synthetic defect with SecY alteration at high temperature.

The secY205 mutant is cold-sensitive for protein export, with an in vitro defect in supporting ATP- and preprotein-dependent insertion of SecA into the membrane. We characterized SecA81 with a Gly516 to Asp substitution near the minor ATP-binding region, which suppresses the secY205 defect at low temperature and exhibits an allele-specific synthetic defect with the same SecY alteration at 42 degrees C. The overproduced SecA81 aggregated in vivo at temperatures above 37 degrees C. Purified SecA81 exhibited markedly enhanced intrinsic and membrane ATPase activities at 30 degrees C, while it was totally inactive at 42 degrees C. The trypsin digestion patterns indicated that SecA81 has some disorder in the central region of SecA, which encompasses residues 421-575. This conformational abnormality may result in unregulated ATPase at low temperature as well as the thermosensitivity of the mutant protein. In the presence of both proOmpA and the wild-type membrane vesicles, however, the thermosensitivity was alleviated, and SecA81 was able to catalyze significant levels of proOmpA-stimulated ATP hydrolysis as well as proOmpA translocation at 42 degrees C. While SecA81 was able to overcome the SecY205 defect at low temperature, the SecY205 membrane vesicles could not significantly support the translocation ATPase or the proOmpA translocation activity of SecA81 at 42 degrees C. The inactivated SecA81 molecules seemed to jam the translocase since it interfered with translocase functions at 42 degrees C. Based on these results, we propose that under preprotein-translocating conditions, the SecYEG channel can stabilize and activate SecA, and that this aspect is defective for the SecA81-SecY205 combination. The data also suggest that the conformation of the central region of SecA is important for the regulation of ATP hydrolysis and for the productive interaction of SecA with SecY.

ATP-Binding Cassette Transporters↗
PubMed1989

Evidence for a light compensation of the inhibition of reproduction by low temperatures in the snail Helix aspersa. Ovotestis and albumen gland responsiveness to different conditions of photoperiods and temperatures.

Four combinations of photoperiods and temperatures have been tested on the reproduction and on the activity of the genital apparatus of the snail Helix aspersa. The results show some interaction between photoperiod and temperature and reveal a predominant effect of photoperiod that compensates for the negative effect of low temperatures. A combination of long day (LD, 18L:6D) and a temperature of 20 degrees C is the most favorable condition for egg-laying as well as for the effective functioning of the ovotestis and albumen gland. In contrast, during a short day (SD, 8L:16D), egg-laying is completely inhibited at 15 degrees C and partly inhibited at 20 degrees C; the differentiation of gametes can be observed in the ovotestis, but the mature oocytes are not released and thus they degenerate. In the albumen gland, an important synthetic activity is noticed, but cellular multiplication and the release of the secretory products decrease. These results suggest that short photoperiods induce inhibition of the (neuro)endocrine centers responsible for the control of both ovulation and egg-laying.

Animals↗
PubMed2001

Determining the temperature distribution of a model vessel wall under pulsed laser irradiation: an experimental attempt to measure fibrous cap thickness and detect temperature elevation in atherosclerotic lesions.

In order to measure the temperature of atherosclerotic plaques, we developed a method to determine the temperature distribution of vessel walls using a three-layer phantom agar model. Under pulsed-laser irradiation, the thickness of upper layer corresponding to fibrous cap overlying the middle layer corresponding to atherosclerotic lesion could be calculated. The temperature was calculated from measured temperature changes under pulsed-laser irradiation.

Aorta↗
PubMed1994

A mathematical analysis of microbial inactivation at linearly rising temperatures: calculation of the temperature rise needed to kill Listeria monocytogenes in different foods and methods for dynamic measurements of D and z values.

From a theoretical analysis of the inactivation of microbes heated at linearly rising temperatures an equation was derived for predicting the linear temperature rise needed to reduce viable numbers of microbes by any chosen factor. This equation is used to predict the temperatures needed to inactivate Listeria monocytogenes in different foods based on published D and z values. Two novel mathematical methods for deriving D and z values from viable counts obtained at linearly rising temperatures are also presented.

Animals↗
PubMed2003

Influence of temperature on tRNA modification in archaea: Methanococcoides burtonii (optimum growth temperature [Topt], 23 degrees C) and Stetteria hydrogenophila (Topt, 95 degrees C).

We report the first study of tRNA modification in psychrotolerant archaea, specifically in the archaeon Methanococcoides burtonii grown at 4 and 23 degrees C. For comparison, unfractionated tRNA from the archaeal hyperthermophile Stetteria hydrogenophila cultured at 93 degrees C was examined. Analysis of modified nucleosides using liquid chromatography-electrospray ionization mass spectrometry revealed striking differences in levels and identities of tRNA modifications between the two organisms. Although the modification levels in M. burtonii tRNA are the lowest in any organism of which we are aware, it contains more than one residue per tRNA molecule of dihydrouridine, a molecule associated with maintenance of polynucleotide flexibility at low temperatures. No differences in either identities or levels of modifications, including dihydrouridine, as a function of culture temperature were observed, in contrast to selected tRNA modifications previously reported for archaeal hyperthermophiles. By contrast, S. hydrogenophila tRNA was found to contain a remarkable structural diversity of 31 modified nucleosides, including nine methylated guanosines, with eight different nucleoside species methylated at O-2' of ribose, known to be an effective stabilizing motif in RNA. These results show that some aspects of tRNA modification in archaea are strongly associated with environmental temperature and support the thesis that posttranscriptional modification is a universal natural mechanism for control of RNA molecular structure that operates across a wide temperature range in archaea as well as bacteria.

Cell Division↗
PubMed1973

Simian virus 40-host cell interactions. I. Temperature-sensitive regulation of SV40 T antigen in 3T3 mouse cells transformed by the ts*101 temperature-sensitive early mutant of SV40.

BALB/3T3 and Swiss/3T3 mouse cells transformed at permissive temperature (33 C) by the early temperature-sensitive mutant of simian virus 40 (SV40), ts(*)101, exhibited a temperature-dependent modulation of SV40 tumor (T) antigen as assayed by immunofluorescence. The percentage of T antigen-positive nuclei in ts(*)101 transformed cells was reduced at restrictive temperature (39 C) when compared to 33 C and to wild-type SV40 transformed cells at either 33 C or 39 C. The percentage of T antigen-positive nuclei in ts(*)101 transformed cells returned to the 33 C control level when the cells were shifted from 39 to 33 C. The ts(*)101 transformed cells could be superinfected with wild-type, but not ts(*)101, virions at 39 C as assayed by an increase in T antigen-positive nuclei.

Adsorption↗
PubMed1992

Differentiation of quail myoblasts transformed with a temperature sensitive mutant of Rous sarcoma virus. II. Relationship of myoblast fusion with calcium and temperature.

The effects of calcium and temperature on fusion of quail embryonic myoblasts were examined using cells transformed with a temperature-sensitive mutant of Rous sarcoma virus (ts-RSV). The transformed quail myoblasts (QM-RSV) fused to form myotubes at 41 degrees C, the non-permissive temperature, but not at 35.5 degrees C, the permissive temperature. On incubation at 41 degrees C, a period of more than 10 hr was needed for the myoblasts to become fusion-competent, but calcium was not needed for development of fusion-competence. Once the cells had become competent, fusion proceeded even at 35.5 degrees C. These results suggest that the src gene product expressed at 35.5 degrees C may control the fusion of cells in the competent stage by inactivating a component(s) that is associated with fusion-competence. However, fusion of even myoblasts in the competent stage was blocked in calcium-deficient medium, suggesting that calcium is essential for the fusion, probably at a step immediately before membrane union. Unlike fusion, other biochemical processes of differentiation proceeded even in calcium-deficient medium, indicating a distinction of fusion from these other processes during myoblast differentiation.

Animals↗
PubMed1991

Effects of temperature on the performance of finishing swine: I. Effects of a hot, diurnal temperature on average daily gain, feed intake, and feed efficiency.

Ninety-six crossbred barrows and gilts weighing 90 +/- .67 kg were used during a 21-d study to determine the effects of a hot, diurnal temperature (H; 22.5 to 35 degrees C) compared with a constant, thermoneutral temperature (TN; 20 degrees C) and the effects of sex (barrows vs gilts) on performance. A secondary objective included the determination of weight loss as a result of a 24-h fast immediately after the 21-d feeding study of commingled vs not commingled hogs of both environmental treatments (TN and H). Pigs housed in the hot, diurnal temperature gained 16.3% more slowly (P less than .001;.77 vs. .92 kg/d) than those in the constant, thermoneutral environment. Feed intake (FI) for the H pigs was 10.9% less (P less than .001; 3.01 vs 3.38 kg/d) than that for the TN pigs. The H pigs gained 17.6 g/d less and consumed 43.5 g/d less feed for every C degrees above 20 degrees C; however, no differences were observed for feed efficiency (F/G; 3.86 vs 4.19 kg for the TN and H pigs, respectively). Average daily gain and feed/gain (F/G) were not affected by sex. Likewise, no significant interactions of temperature x sex were observed for ADG, FI, or F/G. Weight loss (shrinkage) during the 24-h fast was not affected by commingling; however, the H pigs lost 17.5% more weight (P less than .05) than the TN pigs (3.82 vs 3.25%, respectively).

Animals↗
PubMed1985

The primate as a model for the human temperature-sensing system: 1. Adapting temperature and intensity of thermal stimuli.

The thermal sensitivity of three humans and two rhesus monkeys was measured behaviorally, using the "yes-no" paradigm of the Theory of Signal Detection. The aim was to evaluate the monkey's thermal-sensing system as a model for that of humans. Three of the principal variables of human thermal sensations--rate of the temperature change, area of stimulation, and site of stimulation--were held constant. The other three variables--adapting skin temperature (AT), intensity, and direction of the temperature change--were varied systematically. Systematic differences between species were not evident for warming or cooling stimuli. Isodetectability curves (d'e = 1) for small cooling stimuli plotted as a function of the AT were isomorphic, and the points for the human and monkey subjects were frequently superimposed. Isodetectability curves for warming stimuli, on the other hand, had similar shapes for ATs between 33 degrees and 40 degrees C, but the points for the different subjects were not superimposed. At ATs below 30 degrees C, one of the two humans in the warming series and the two monkeys continued to show similarly shaped curves, but the other human was markedly different. Qualitative descriptions of the thermal sensations obtained during threshold measurements of human subjects, reported previously, suggest that this unusual subject probably adopted a criterion qualitatively different from that used by the other subjects. The data presented here and in combination with previously published work from this laboratory (Kenshalo, 1970) suggest that thermal stimuli produce similar sensations in rhesus monkeys and humans, and that the neural systems responsible for coding AT and temperature change in the two species are fundamentally similar.

Adaptation, Physiological↗
PubMed1995

Temperature-induced changes in the number of vesicles in the free nerve endings of temperature neurons of the snake.

By observing ultrastructural changes under the electron microscope, we illustrated exocytosis and recycling of vesicles in the infrared receptor, a kind of free nerve ending in the pit organ of the crotaline snake, Trimeresurus flavoviridis. While maintaining the snake pit organs at stable temperatures of 15 degrees C, 25 degrees C, and 30 degrees C, we fixed them by perfusion and then processed them for transmission electron microscopy. The largest number of clear and coated vesicles appeared in the terminals at the lowest temperature. The perimeter and area of a terminal were enlarged at 30 degrees C, and "opening waves" on the plasma were prominently found at the highest temperature. We also observed coated vesicles that budded from the plasma membrane in the terminals. The configuration of mitochondria in the terminals was quantitatively different between lower and higher temperatures. The data suggest that exocytosis and endocytosis in these terminals operate in a manner similar to that observed in other cell types.

Animals↗
PubMed1999

Response surface models for effects of temperature and previous temperature on lag time and specific growth rate of Salmonella Typhimurium on cooked ground chicken breast.

Response surface models were developed for effects of temperature (16 to 34 degrees C) and previous temperature (pretemperature; 16 to 34 degrees C) on lag time (lambda) and specific growth rate (mu) of Salmonella Typhimurium on cooked ground chicken breast. The primary objective was to determine whether pretemperature is a major factor affecting growth of Salmonella Typhimurium. Growth curves for model development (n = 32) and model testing (n = 18) were fit to a two-phase linear equation that directly estimated lambda and mu. Response surface models for ln lambda and ln mu as a function of temperature and pretemperature were obtained by regression analysis. Lag time and mu of Salmonella Typhimurium were affected by temperature but not pretemperature. Models were tested against data not used in their development. Prediction error (model accuracy) was 13.4% for lambda and 11.3% for mu, whereas the median relative error of predictions (model bias) was -3.0% for lambda and 6.8% for mu. Results indicated that the models provide reliable predictions of lambda and mu of Salmonella Typhimurium on cooked ground chicken breast within the matrix of conditions modeled. In addition, pretemperature (16 to 34 degrees C) is not a major factor affecting growth of Salmonella Typhimurium.

Animals↗
PubMed1989

[Temperature influence on human testicular function--optimal temperature for testicular macromolecular synthesis].

Precursor incorporations into DNA, RNA and protein fractions of the human testicular tissue were examined at 28 degrees C-43 degrees C in vitro to study the optimal temperature for DNA, RNA and protein synthesis in the human testis. The results suggest that the DNA synthesis shows delicate temperature sensitivity and is at a maximum at 31 degrees C, whereas the RNA and protein syntheses are at a maximum at 37 degrees C-40 degrees C. The slight variation of the testicular temperature may cause spermatogenic dysfunction because of delicate temperature sensitivity of the testicular DNA synthesis.

Culture Techniques↗
PubMed1999

[The plasmid carrying the temperature-sensitive mutation in the DNa-methylase gene of the PStI system: effect on host cells at nonpermissive temperature].

Temperature-sensitive (ts) derivatives of plasmid pRMP1, the derivative of PBR322 containing restriction and modification (RM) genes of the PstI system, were obtained using hydroxylamine mutagenesis. One of the isolated plasmids responsible for the inhibition of Escherichia coli cell growth at 42 degrees C, pRMPts, was analyzed in this work. Cells of Rec+ strains carrying this plasmid were unable to divide at 42 degrees C and formed long non-septated filaments that died upon prolonged cultivation. Cells of the RecA- strains carrying pRMPts did not form filaments at 42 degrees C and rapidly disappeared. On agar media with or without ampicillin, Rec+ and RecA- strains with this plasmid formed colonies of temperature-resistant (tr) derivatives with frequencies ranging from 1.5 x 10(-4) to 4 x 10(-6) in independent clones. The structure of plasmids from cells of tr-derivatives of Rec+ and RecA- strains carrying plasmid pRMPts was analyzed by the set of restriction enzymes. Reversions to the temperature-resistant phenotype were shown to result from the following events: (1) the insertional inactivation of the PstI restriction enzyme gene in pRMPts (the insertion of the IS1 element); (2) deletions in plasmid DNA fragments that partially or completely cover the restriction enzyme gene; (3) point mutations; and (4) others. The effect of the chromosomal sulA mutation on the maintenance of the ts-plasmid in bacterial cells was studied at 42 degrees C. High efficiency loss of the plasmid was detected in pRMPts-carrying Rec+ cells with the sulA::Tn5 mutation grown in liquid and solid nutrient media at this temperature. Under similar conditions, plasmid loss was not detected in SulA+ cells. On the basis of the data obtained, it is concluded that the ts-mutation is located in the DNA-methylase gene of plasmid pRMPts. Mutant DNA methylase was unable to methylate all sites in the chromosomal DNA at 42 degrees C. Some of the unmethylated sites can be digested with the PstI enzyme, which leads to the induction of SOS response in Rec+ cells or to total mortality in cells with the recA phenotype.

Bacterial Proteins↗
PubMed2001

Use of intravesical temperature as a monitor of core temperature during and following general anaesthesia.

OBJECTIVE: The value of thermistor-bearing urinary catheters has not been extensively investigated in the postoperative period. This study compared thermistor-bearing urinary catheters with pulmonary artery catheters as a means of measuring core temperature during and following general anaesthesia in patients undergoing aortic aneurysmectomy. METHODS: Information was obtained from 16 patients divided into two equal groups; one group provided intra-operative data, and the other group postoperative data. Simultaneous temperature measurements were obtained from each of the catheters at specific time intervals--every 10 minutes for the duration of anaesthesia and every 30 minutes for 10 hours during the postoperative period. RESULTS: Agreement between the two catheters and the accuracy and precision of the intravesical catheter with regard to the pulmonary artery catheter were determined. Clinically acceptable limits of agreement between the two methods of measurement were noted, although the limits of agreement were somewhat better for the postoperative period. During the early intra-operative period the intravesical catheter tended to over-read the pulmonary artery catheter, the largest mean difference being +0.3 degree C. During the postoperative period the intravesical catheter either under-read or over-read the pulmonary artery catheter, depending on whether core temperature was rising or falling. Mean differences varied from +0.2 degree C to -0.1 degree C. However, neither during the intra-operative nor the postoperative periods were statistically significant differences noted between the two measurement methods. CONCLUSION: The study indicates that in patients undergoing aortic aneurysmectomy, the thermistor-bearing urinary catheter is a clinically acceptable measure of core temperature during and following general anaesthesia.

Anesthesia, General↗
PubMedDate not supplied

[The temperature dependence of high-resolution 1H NMR spectra of Rhodobacter sphaeroides photosynthetic reaction centres in a temperature range of 25-40 degrees C].

High-resolution 1H-NMR spectra registered within a temperature range of 25-40 degrees C revealed a nonmonotonous dome-shaped temperature dependence of the ratio between integral NMR signal intensities determined at ppm intervals 2.5-4.5 and 0.2-2.5 with a maximum at 30 degrees C. This may be due to RC structural changes accompanying the temperature rise and accelerating the recombination reaction between oxidized bacteriochlorophyll and reduced primary quinone at temperatures above 30 degrees C.

Electron Transport↗
PubMed1987

A temperature-compensated ultradian clock explains temperature-dependent quantal cell cycle times.

The effects of sublethal heat pulses on cell division have provided insights into possible molecular mechanisms. Thus Zeuthen's findings of 'set-backs' up to a transition point provides the basis for the idea that the continuous accumulation of a compound needed for cell division spans a major portion of the cell cycle. The accumulating substance is a 'division protein' which forms part of a structure which is unstable until completely assembled at the transition point. Experiments showing phase resetting of mammalian cells by temperature perturbation indicate limit-cycle oscillator control of the cell cycle with a phase-response curve with a repeat interval equal to the period of the clock. As well as providing a method for establishing synchronized cultures these observations have found application in the selective effects of hyperthermia as an antitumour agent. Circadian rhythms display several unique features distinguishing them from other periodic processes. Only recently has it been recognized that some of these characteristics may be properties of ultradian rhythms as well. The probably most striking feature of circadian timekeeping, i.e. independence of ambient temperature, was found for ultradian rhythmicity even at the level of the unicellular organization. Synchronous cultures of some lower eukaryotes were prepared by centrifugal size selection methods. Experiments with asynchronous control cultures substantiated the view that the conditions employed were such as to minimize any perturbative effects: most importantly the organisms were never removed from their culture medium. Whereas the control cultures showed smoothly increasing respiration rates, total RNA, total protein, enzyme activities and enzyme protein (e.g. for cytochrome aa3, ATPase, catalase), in synchronous cultures all these parameters showed oscillatory behaviour. Different periods were observed in different organisms: thus in Acanthamoeba castellanii the period was about 70 min, in Tetrahymena pyriformis strain ST it was about 50 min, in T. pyriformis AII it was 30 min, and in Candida utilis it was about 30 min (all measurements at 30 degrees C). In A. castellanii the periods of both the oscillations in rate of respiration and the total cell protein were hardly affected by the temperature of growth over the range 20 to 30 degrees C. The oscillations show no damping during experiments lasting 12 h: these properties suggest that we are observing temperature-compensated endogenous rhythms which presumably serve a timekeeping function in cells undergoing growth and division.(ABSTRACT TRUNCATED AT 400 WORDS)

Activity Cycles↗