Effect of temperature on intracellular pH in crayfish neurons and muscle fibers

1984 ◽  
Vol 246 (1) ◽  
pp. C45-C49 ◽  
Author(s):  
J. L. Rodeau
Keyword(s):  
Intracellular Ph ◽  
Muscle Fibers ◽  
Effect Of Temperature ◽  
Cellular Regulation ◽  
Acid Base ◽  
Astacus Leptodactylus ◽  
Acid Base Status ◽  
Effects Of Temperature ◽  
Ph Microelectrodes

Intracellular pH microelectrodes were used to determine the effects of temperature (13-26 degrees C) on the in vitro regulation of intracellular acid-base status of neurons and muscle fibers of the crayfish Astacus leptodactylus. The values of the temperature coefficients delta pH/delta T (pH unit/degrees C) were -0.019 and -0.026 for muscles and neurons, respectively, values which are close to the temperature coefficient (-0.019) of the pK' of protein imidazole buffer groups. When temperature varies, the dissociation ratio of imidazole groups is thus maintained by the cellular regulation of cytoplasmic pH. According to the alphastat regulation hypothesis, this constancy would minimize the temperature effects on enzymic systems.

Effects of temperature and acid-base state on hippocampal population spikes in hamsters

1990 ◽  
Vol 258 (5) ◽  
pp. R1140-R1146 ◽  
Author(s):  
P. Eckerman ◽  
K. Scharruhn ◽  
J. M. Horowitz
Keyword(s):  
Hippocampal Slices ◽  
Pyramidal Cells ◽  
Effect Of Temperature ◽  
Acid Base ◽  
Bathing Medium ◽  
Maximal Stimulation ◽  
Synchronous Firing ◽  
Acid Base Status ◽  
Effects Of Temperature ◽  
Induced Changes

Previous studies have shown that changes in temperature, within the range encountered by hamsters entering hibernation, alter the evoked response of hippocampal pyramidal cells to stimulation of an afferent pathway. The present study was designed to determine whether these alterations are due to changes in the acid-base status of the neural tissue brought about by changes in temperature. Extracellular-evoked responses were recorded from hamster hippocampal slices after Schaffer collateral stimulation. The pH was changed by varying the concentration of CO2 aerating the bathing medium. Buffers contained either 26 or 40 mM bicarbonate ion. The width of the population spike (the synchronous firing of pyramidal cells) was measured as pH was varied between 7.5 and 7.1, with slice temperature set at either 25 or 20 degrees C. There was a significant increase in spike width as temperature was lowered to 20 degrees C, but no significant change in spike width or amplitude as pH or bicarbonate was varied. The effect of temperature (20 degrees C for half-maximal stimulation, and from 20 to 25 degrees C for just maximal stimulation) on spike width and amplitude thus does not appear to be due to pH- or bicarbonate-induced changes.

scholarly journals Temperature Effects on Haemolymph Acid-Base Status In Vivo and In Vitro in the Two-Striped Grasshopper Melanoplus Bivittatus

1988 ◽  
Vol 140 (1) ◽  
pp. 421-435 ◽  
Author(s):  
JON M. HARRISON
Keyword(s):  
Body Temperature ◽  
Carbonic Acid ◽  
Temperature Shift ◽  
Effect Of Temperature ◽  
Locomotory Activity ◽  
Acid Base ◽  
Protein Dissociation ◽  
Acid Base Status

In this study, I examine the effect of temperature on haemolymph acid-base status in vivo and in vitro in the two-striped grasshopper Melanoplus bivittatus. Melanoplus bivittatus experience wide (up to 40 °C) diurnal body temperature fluctuations in the field, but maintain body temperature relatively constant during sunny days by behavioural thermoregulation. Haemolymph pH was statistically constant (7.12) between 10 and 25°C, but decreased by −0.017 units °C− from 25 to 40°C. Relative alkalinity and fractional protein dissociation were conserved only at body temperatures at which feeding and locomotory activity occur, above 20°C. Haemolymph total CO2 (Ctot) increased from 10 to 20°C and decreased from 20 to 40°C. Haemolymph Pco2 increased from 10 to 20°C and was statistically constant between 20 and 40°C. Carbonic acid pKapp in haemolymph was 6.122 at 35°C, and decreased with temperature by −0.0081 units°C−1. Haemolymph buffer value averaged −35mequivl−1pHunit−1. Haemolymph pH changes with temperature were small (less than −0.004 units°C−1) in vitro at constant Pco2. Therefore, passive physicochemical effects cannot account for the pattern of acid-base regulation in vivo. The temperature shift from 10 to 20°C was accompanied by a net addition of 4.2-6.2 mmoll−1 of bicarbonate equivalents to the haemolymph. The temperature shift from 20 to 40°C was accompanied by a net removal of 10–14 mmoll−1 of bicarbonate equivalents from the haemolymph. Haemolymph acid-base regulation in vivo during temperature changes is dominated by active variation of bicarbonate equivalents rather than by changes in Pco2 as observed for most other air-breathers.

scholarly journals Effects of temperature on in vitro response of Trichoderma strains against strawberry pathogen Rhizoctonia solani Kühn.

2017 ◽  
Vol 38 (SI 2 - 6th Conf EFPP 2002) ◽  
pp. 620-622
Author(s):  
M. Porras ◽  
C. Barrau ◽  
B. Santos ◽  
F.T. Arroyo ◽  
C. Blanco ◽  
...  
Keyword(s):  
Rhizoctonia Solani ◽  
Analysis Of Variance ◽  
Radial Growth ◽  
Local Strain ◽  
Effect Of Temperature ◽  
Trichoderma Spp ◽  
Inhibiting Effect ◽  
In Vitro Response ◽  
Effects Of Temperature

Effect of temperature on growth and antagonistic ability of Trichoderma spp. isolated from local strawberry culture and commercial product, against Rhizoctonia solani, strawberry pathogen, was studied in vitro. Trials were carried out twice, at 10, 25 and 30°C. Inhibitor effect was evaluated by radial growth measures of established duals on PDA’s dishes, using Royse and Ries formula, to evaluate the percentage inhibition of radial growth. Design of dishes was a randomized complete block, considering 10 replicates. Data were analyzed statistically by two-way analysis of variance. The objective has been to determine the most competitive Trichoderma strain and the best temperature that produce the inhibiting effect on the pathogen growth. Local strain has the best behavior at 10 and 25°C.

Flow and thermal responses of aortic baroreceptors

1993 ◽  
Vol 70 (6) ◽  
pp. 2596-2605 ◽  
Author(s):  
P. A. Munch
Keyword(s):  
Aortic Arch ◽  
Neural Control ◽  
Effect Of Temperature ◽  
Wide Range ◽  
Activation Response ◽  
Flow Through ◽  
Effects Of Temperature ◽  
Aortic Arch Pressure ◽  
Aortic Baroreceptors

1. The aims of this study were 1) to determine whether the impulse activity in rabbit aortic baroreceptors (BRs) was influenced by changes in nonpulsatile flow through the aortic lumen and 2) to examine the BR and aortic arch responses to changes in temperature. 2. An in vitro aortic arch-aortic nerve preparation was used to record suprathreshold steady-state discharge in a total of 29 single-unit BRs from 12 New Zealand white rabbits. Changes in BR frequency were measured relative to control and were recorded simultaneously with aortic arch pressure, flow, temperature, diameter, and calculated wall shear stress (Sw). 3. With pressure held constant, stair-step increases in flow (3–18 ml/min) constricted the arch and evoked two types of BR responses: activation in most units (15 of 17 BRs tested) and inhibition in 2 units. The activation response appeared closely related to the changes in flow and Sw, but also appeared related to uncontrolled changes in perfusate temperature. 4. When the effects of temperature were examined more closely with pressure and flow held constant, controlled step increases in temperature (between 32 and 42 degrees C) constricted the arch and again evoked two BR responses: activation in 11 of 14 BRs tested and inhibition in 3 units. The Q10 for the activation response was 1.55 +/- 0.08 (mean +/- SE), which was not significantly different from the Q10 for activation when temperature varied with flow (1.65 +/- 0.1, P < 0.05). Thus the effect of temperature on most BRs was directionally and quantitatively similar in the presence and absence of changes in flow. 5. Last, when flow was examined over a wide range (15–515 ml/min) with temperature and pressure held constant, stair-step increases in flow failed to produce any change in BR frequency in each of 15 fibers tested (10 arches). The lack of response was not due to a functionally damaged preparation because the usual BR and aortic arch responses to pressure and to drug-evoked vasoconstriction (norepinephrine) and endothelial-mediated vasodilation (acetylcholine) were intact. 6. These results demonstrate that aortic BRs in rabbits are not sensitive to flow and thus are not likely influenced by fluctuations in cardiac output apart from associated changes in pressure. The aortic BRs are affected directly by variations in temperature and in some cases indirectly by temperature-related vasoconstriction. The effects of temperature may have important implications for neural control of the circulation when core temperature varies because of physiological and environmental stress.

Changes in uterine fluid composition and acid-base status during shell formation in the chicken

1989 ◽  
Vol 257 (4) ◽  
pp. R732-R737 ◽  
Author(s):  
Z. Arad ◽  
U. Eylath ◽  
M. Ginsburg ◽  
H. Eyal-Giladi
Keyword(s):  
Sharp Increase ◽  
Blood Gases ◽  
Future Application ◽  
Epithelial Tissue ◽  
Fluid Composition ◽  
Acid Base ◽  
Co2 Partial Pressure ◽  
Uterine Fluid ◽  
Acid Base Status

The aim of this study was to characterize the dynamic changes in uterine fluid composition and acid-base status during shell calcification in the chicken. Uterine eggs at timed intervals were manually aborted and the accompanying fluid collected and analyzed for composition of osmolytes, enzymes, and acid-base parameters. Blood samples were analyzed for comparison. No considerable change in blood gases took place in relation to residence time of the calcifying egg in the uterus. A significant acidosis occurred at latter stages. Only minor changes were revealed in plasma osmotic and biochemical composition throughout egg calcification. In contrast, major changes were revealed in uterine fluid composition and acid-base status during calcification. The most prominent phenomenon was the sharp increase in CO2 partial pressure, from 82.2 Torr at 0 h to 132.8 Torr at 10 h. As bicarbonate concentration remained almost stable, fluid pH dropped from 7.412 to 7.250 within this stage. Uterine fluid sodium and chloride concentrations and osmolality dropped significantly in the course of calcification, whereas potassium concentration significantly increased. A sharp increase in glucose, calcium, and magnesium concentrations was measured in the early stages of calcification. These findings are discussed in relation to existing models for transport mechanisms of the uterine epithelial tissue. The comprehensive picture that emerges from the present study should enable future application in establishing a self-contained culturing system in vitro for studies of embryonic development.

EFFECT OF TEMPERATURE ON METABOLIC RATES OF LIVER AND BROWN FAT HOMOGENATES

1967 ◽  
Vol 45 (11) ◽  
pp. 1763-1771 ◽  
Author(s):  
Jane C. Roberts ◽  
Robert E. Smith
Keyword(s):  
Adipose Tissue ◽  
Oxygen Consumption ◽  
Brown Adipose Tissue ◽  
Brown Fat ◽  
Effect Of Temperature ◽  
Metabolic Rates ◽  
Brown Adipose ◽  
Rate Of Oxygen Consumption ◽  
Effects Of Temperature

The effects of temperature in vitro upon metabolic rates of homogenates of brown fat and liver from control and cold-acclimated rats have been examined over the range 10–37 °C. At all temperatures, brown adipose tissue exhibits a higher rate of oxygen consumption [Formula: see text] than does liver, α-ketoglutarate being used as substrate. At 10 °C, brown adipose tissue retains a larger percentage (36–38%) of its 37 °C metabolic rate than does liver (22–24%).Q10 values and energies of activation (Ea) have been determined and compared with other data reported for these tissues. At 20 °C, breaks appear in the Arrhenius plots for liver from both control and cold-acclimated rats and also for brown fat from control rats, but not for the brown fat from cold-acclimated rats. Thus brown adipose tissue from cold-acclimated rats retains relatively higher levels of respiration at temperatures below the 20 °C breaking point than does brown fat from control rats.In view of previously reported cold-induced increases in mass, vascularity, and [Formula: see text] of brown fat, this decreased temperature sensitivity in the cold-acclimated rats appears wholly consonant with the adaptive behavior of brown fat in its role as a thermogenic effector.

Cellular actions of cAMP on HCO3(-)-secreting cells of rabbit CCD: dependence on in vivo acid-base status

1994 ◽  
Vol 266 (4) ◽  
pp. F528-F535 ◽  
Author(s):  
C. Emmons ◽  
J. B. Stokes
Keyword(s):  
Anion Exchanger ◽  
Collecting Duct ◽  
Basolateral Membrane ◽  
Disulfonic Acid ◽  
Intercalated Cells ◽  
Cortical Collecting Duct ◽  
Acid Base ◽  
Acid Base Status

HCO3- secretion by cortical collecting duct (CCD) occurs via beta-intercalated cells. In vitro CCD HCO3- secretion is modulated by both the in vivo acid-base status of the animal and by adenosine 3',5'-cyclic monophosphate (cAMP). To investigate the mechanism of cAMP-induced HCO3- secretion, we measured intracellular pH (pHi) of individual beta-intercalated cells of CCDs dissected from alkali-loaded rabbits perfused in vitro. beta-Intercalated cells were identified by demonstrating the presence of an apical anion exchanger (cell alkalinization in response to removal of lumen Cl-). After 180 min of perfusion to permit decrease of endogenous cAMP, acute addition of 0.1 mM 8-bromo-cAMP or 1 microM isoproterenol to the bath caused a transient cellular alkalinization (> 0.20 pH units). In the symmetrical absence of either Na+, HCO3-, or Cl-, cAMP produced no change in pHi. Basolateral dihydrogen 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid (0.1 mM) for 15 min before cAMP addition also prevented this alkalinization. In contrast to the response of cells from alkali-loaded rabbits, addition of basolateral cAMP to CCDs dissected from normal rabbits resulted in an acidification of beta-intercalated cells (approximately 0.20 pH units). The present studies demonstrate the importance of the in vivo acid-base status of the animal in the regulation of CCD HCO3- secretion by beta-intercalated cells. The results identify the possible existence of a previously unrecognized Na(+)-dependent Cl-/HCO3- exchanger on the basolateral membrane of beta-intercalated cells in alkali-loaded rabbits.

Skeletal muscle fatigue in vitro is temperature dependent

1986 ◽  
Vol 61 (2) ◽  
pp. 660-665 ◽  
Author(s):  
S. S. Segal ◽  
J. A. Faulkner ◽  
T. P. White
Keyword(s):  
Effect Of Temperature ◽  
Isometric Contractions ◽  
Temperature Dependent ◽  
Temperature Optimum ◽  
Constant Frequency ◽  
Protocol Development ◽  
Effects Of Temperature ◽  
The Relationship ◽  
Bell Shaped Curve

Our purpose was to determine the effect of temperature on the fatigability of isolated soleus and extensor digitorum longus (EDL) muscles from rats during repeated isometric contractions. Muscles (70–90 mg) were studied at 20–40 degrees C in vitro. Fatigability was defined with respect to both the time and number of stimuli required to reach 50% of the force (P) developed at the onset of the fatigue test. Fatigue was studied during stimulation protocols of variable [force approximately 70% of maximum force (Po)] and constant frequency (28 Hz). Results for soleus and EDL muscles were qualitatively similar, but fatigue times were longer for soleus than for EDL muscles. During the variable-frequency protocol, development of approximately 70% of Po required an increase in stimulation frequency as temperature increased. During stimulation at these frequencies, fatigue time shortened as temperature increased. For both fatigue protocols, the relationship between temperature and the number of stimuli required to reach fatigue followed a bell-shaped curve, with maximum values at 25–30 degrees C. The temperature optimum for maximizing the number of isometric contractions to reach fatigue reflects direct effects of temperature on muscle function.

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