Basolateral membrane chloride permeability of A6 cells: implication in cell volume regulation

The permeability to Cl^– of the basolateral membrane (blm) was investigated in renal (A6) epithelial cells, assessing their role in transepithelial ion transport under steady-state conditions (isoosmotic) and following a hypoosmotic shock (i.e. in a regulatory volume decrease, RVD). Three different complementary studies were made by measuring: (1) the Cl^– transport rates (F/F _o · s^–1 (× 10^–3)), where F is the fluorescence of N-(6-methoxyquinoyl) acetoethyl ester, MQAE, and F _o the maximal fluorescence (×10^–3) of both membranes by following the intracellular Cl^–3 activities (a _iCl^–, measured with MQAE) after extracellular Cl^– substitution (2) the blm ⁸⁶Rb and ³⁶Cl uptakes and (3) the cellular potential and Cl^– current using the wholecell patch-clamp technique to differentiate between the different Cl^– transport mechanisms. The permeability of the blm to Cl^– was found to be much greater than that of the apical membranes under resting conditions: a _iCl^– changes were 5.3±0.7 mM and 25.5±1.05 mM (n=79) when Cl^– was substituted by NO₃ ^– in the media bathing apical and basolateral membranes. The Cl^– transport rate of the blm was blocked by bumetanide (100 M) and 5-nitro-2-(3-phenylpropylamino)benzoic acid (NPPB, 50 M) but not by N-phenylanthranilic acid (DPC, 100 M). ⁸⁶Rb and ³⁶C1 uptake experiments confirmed the presence of a bumetanide- and a NPPB-sensitive Cl^– pathway, the latter being approximately three times more important than the former (Na/K/2Cl cotransporter). Application of a hypoosmotic medium to the serosal side of the cell increased F/F _o · s^–1 (×10^–3) after extracellular Cl^–3 substitution (1.03±0.10 and 2.45±0.17 arbitrary fluorescent units·s^–1 for isoosmotic and hypoosmotic conditions respectively, n=11); this F/F _o·s^–1 (×10^–3) increase was totally blocked by serosal NPPB application; on the other hand, cotransporter activity was decreased by the hypoosmotic shock. Cellular Ca²⁺ depletion had no effect on F/F _o·s^–1 (×10^–3) under isoosmotic conditions, but blocked the F/F _o·s^–1 (×10^–3) increase induced by a hypoosmotic stress. Under isotonic conditions the measured cellular potential at rest was –37.2±4.0 mV but reached a maximal and transient depolarization of –25.1±3.7 mV (n=9) under hypoosmotic conditions. The cellular current at a patch-clamping cellular potential of –85 mV (close to the Nernst equilibrium potential for K⁺) was blocked by NPPB and transiently increased by hypoosmotic shock ( 50% maximum increase). This study demonstrates that the major component of Cl^– transport through the blm of the A6 monolayer is a conductive pathway (NPPB-sensitive Cl^– channels) and not a Na/K/2Cl cotransporter. These channels could play a role in transepithelial Cl^– absorption and cell volume regulation. The increase in the blm Cl^– conductance, inducing a depolarization of these membranes, is proposed as one of the early events responsible for the stimulation of the ⁸⁶Rb efflux involved in cell volume regulation.     

Comparison of the buffer capacity of endocytotic vesicles,lysosomes and cytoplasm in cells derived from the proximal tubule of the kidney (opossum kidney cells)

During transepithelial acid-base transport cells of the proximal tubule of the kidney have to maintain a relative constant intracellular pH. Herein cellular buffer capacity plays an important role. We measured vesicular buffer capacity in proximal tubule-derived opossum kidney cells and compared it with cytoplasmic buffer capacity to determine the possible importance of vesicular buffer capacity for cellular pH homeostasis. Under HCO₃ ^–-free conditions endocytotic vesicular buffer capacity was 43±4 mmol·l^–1·pH-unit^–1 (n=7) and exceeded cytoplasmic buffer capacity (19±3 mmol·l^–1 ·pH-unit^–1; n=7) significantly. Lysosomal buffer capacity was 19±6 mmol·l^–1·pH-unit^–1; (n=5). Inhibition of vesicular H⁺-ATPase using bafilomycin A₁ led to a dramatic increase of vesicular pH but to a decrease of cytoplasmic pH indicating the importance of organellar buffer systems. We estimated that endocytotic buffer capacity accounts for 23% of cellular buffer capacity under our experimental condition and thus, impairment of endosomal acidification may affect cytoplasmic pH indeed. From our results we conclude that endocytotic vesicles have a large buffer capacity and might play a role in cellular pH homeostasis.     

Electrically evoked isometric and isokinetic properties of the triceps surae in young male subjects

Summary The relationship between electrically evoked isometric and isokinetic properties of the triceps surae have been studied in 11 healthy male subjects. The results showed that the time to peak tension (TPT) and half relaxation time (1/2 RT) of the maximal twitch were 110±11 ms and 82±11 ms respectively, and the peak rates of rise of contraction (P ₅₀, P ₂₀₀) and relaxation (P _R50, P _R200) at 50 and 200 Hz were 0.36±0.07, 0.48±0.08 and 1.27±0.33, 1.25±0.27% Po ms^–1 respectively. The decline in force during a fatigue test was significantly (P<0.02) associated with the decrease in maximal relaxation rate (r=0.79). The TPT was significantly (P<0.05) and inversely related to P ₅₀ and P ₂₀₀. The mean angle specific torque-velocity relationship for the 11 subjects was adequately described by the empirical exponential equation of the form: V=16.5 (e ^–p/30.8–e ^–84.3/30.8) where V=velocity (rads s^–1) P=torque (Nm). The only significant association found between the isometric and isokinetic properties of the muscle was between P _R200 and the torque expressed at a given velocity of 4 rads s^–1. This lack of association between the two variables is difficult to explain with certainty but it is suggested that it may be due to the differential effects of Ca²⁺ release and uptake and cross-bridge turnover rate in the two situations.     

Characterization of two MDCK-cell subtypes as a model system to study principal cell and intercalated cell properties

Madin-Darby canine kidney (MDCK) cells originate from the renal collecting duct and consist of different cell subtypes. We cloned two MDCK cell subtypes denominated as C7 and C11 with different morphology and different function. The two clones maintained their functional differences after cloning. C7 monolayers exhibit a high transepithelial resistance (R _te=5648±206 · cm², n=20) and secrete K⁺ (K⁺=1.31±0.08 mmol/l, n=10) into the apical medium. C11 monolayers display a low R _te (330±52 · cm², n=20) and secrete Cl^– (Cl^–= 16.9±1.8 mmol/l, n=10) into the apical medium. Aldosterone (1 mol/l) stimulates K⁺ secretion (K⁺ of 3.58±0.11 mmol/l, n=7) in C7 cells and H⁺ secretion in C11 cells (pH=0.060±0.007, n=10). Aldosterone-induced stimulation of K⁺ secretion is inhibited by apical application of amiloride (1 mol/l). cAMP stimulates H⁺ secretion in C11 cells (pH= –0.068±0.004, n=10). Furthermore, C7 cells are peanut-lectin(PNA)-negative and exhibit an intracellular pH of 7.39±0.05 (n=7), whereas C11 cells maintain intracellular pH at 7.16±0.05 (n=8) and a major fraction of cells is PNA positive. We conclude that we have cloned two subtypes of MDCK cells which stably express different functional characteristics. The C7 subtype resembles principal cells (PC) of the renal collecting duct, whereas the C11 subtype resembles intercalated cells (ICC) of the renal collecting duct. The C11 subtype seems heterogenous and possibly consists of two subpopulations similar to the -ICC and -ICC of the renal collecting duct. The two cloned subtypes could serve as a valuable model to study PC-like cells and ICC-like cells independently.     

Static and dynamic activity of warm receptors in Boa constrictor

Summary Afferent impulses from multi- and single-fiber preparations of the trigeminal nerve inBoa constrictor were recorded during exactly controlled thermal stimulation of the receptive field in the labial region. At constant temperatures in the range between 18 and 37°C, multi-fiber preparations showed a continuous discharge with a maximum around 30°C. Dynamic warming caused a high increase of the discharge, whereas dynamic cooling led to a complete inhibition. No cold-sensitive fibers have been found. Mechanical stimulation elicited large spikes from specific mechanoreceptors.Single-fiber preparations from labial warm receptors did not respond to mechanical stimulation. Their discharge was always regular at constant temperatures. The average frequency of a warm receptor population was zero at about 18°C, reached a maximum of 13 sec^–1 at 30°C and fell again to zero at 37°C. In addition, a few warm receptors increased their static discharge with temperature up to 36°C, the highest frequency being 38 sec^–1. Stepwise warming by T=+5°C caused a marked overshoot in frequency, after which the discharge usually fell to a minimum and then rose again to a new static level. Stepwise cooling by T=–5°C led to a transient inhibition of activity followed by an increase until the new static level was reached. In the first group of warm receptors the height of the dynamic overshoot varied with the adapting temperature, the largest average overshoot of 160 sec^–1 occurring at an adapting temperature of 30°C. These receptors have their static maximum as well as their highest dynamic sensitivity in the temperature range of the natural tropical habitat of Boidae.Supported by a grant from the Deutsche Forschungsgemeinschaft     

Ventilatory responses to exercise and carbon dioxide in elderly and younger humans

Summary The present investigation examined the relationship between CO₂ sensitivity [at rest (S _R) and during exercise (S _E)] and the ventilatory response to exercise in ten elderly (61–79 years) and ten younger (17–26 years) subjects. The gradient of the relationship between minute ventilation and CO₂ production ( _E/ CO₂) of the elderly subjects was greater than that of the younger subjects [mean (SEM); 32.8 (1.6) vs 27.3 (0.4); P<0.01]. At rest, S _R was lower for the elderly than for the younger group [10.77 (1.72) vs 16.95 (2.13) 1 · min^–1 · kPa^–1; 1.44 (0.23) vs 2.26 (0.28) 1 · min^–1 · mmHg^–1; P<0.05], but S _E was not significantly different between the two groups [17.85 (2.49) vs 19.17 (1.62) l · min^–1 · kPa^–1; 2.38 (0.33) vs 2.56 (0.21) 1 · min^–1 · mmHg^–1]. There were significant correlations between both S _R and S _E, and _E/ CO₂ (P<0.05; P<0.001) for the younger group, bot none for the elderly. The absence of a correlation for the elderly supports the suggestion that _E/ CO₂ is not an appropriate index of the ventilatory response to exercise for elderly humans.     

Effect of endurance training on excessive CO2 expiration due to lactate production in exercise

Summary We attempted to determine the change in total excess volume of CO₂ Output (CO₂ excess) due to bicarbonate buffering of lactic acid produced in exercise due to endurance training for approximately 2 months and to assess the relationship between the changes of CO₂ excess and distance-running performance. Six male endurance runners, aged 19–22 years, were subjects. Maximal oxygen uptake (VO_2max), oxygen uptake (VO₂) at anaerobic threshold (AT), CO₂ excess and blood lactate concentration were measured during incremental exercise on a cycle ergometer and 12-min exhausting running performance (12-min ERP) was also measured on the track before and after endurance training. The absolute magnitudes in the improvement due to training for C02 excess per unit of body mass per unit of blood lactate accumulation (Ala^–) in exercise (CO₂ excess·mass^–1·la^–), 12-min ERP, VO₂ at AT (AT-VO₂) and VO_2max on average were 0.8 ml·kg^–1·l^–1·mmol^–1, 97.8m, 4.4 ml·kg^–1· min^–1 and 7.3 ml·kg^–1·min^–1, respectively. The percentage change in CO₂ excess·mass^–1·la^– (15.7%) was almost same as those of VO_2max (13.7%) and AT-VO₂ (13.2%). It was found to be a high correlation between the absolute amount of change in CO₂ excess·mass^–1·la^– and the absolute amount of change in AT-VO₂ (r=0.94, P<0.01). Furthermore, the absolute amount of change in C02 excess·mass^–1·la^–, as well as that in AT-VO₂ (r=0.92, P<0.01), was significantly related to the absolute amount of change in 12-min ERP (r=0.81, P<0.05). It was concluded that a large CO₂ excess·mass^–1·la^–1 of endurance runners could be an important factor for success in performance related to comparatively intense endurance exercise such as 3000–4000 m races.     

Seasonal changes in plasma and aortic lipids in young rats

Summary In young non-exercised rats, plasma triglyceride and plasma phospholipid levels increased in summer and low density lipoprotein cholesterol (LDL-C) increased in winter. As for lipids samples from the wall of the aorta, total cholesterol, cholesteryl ester and triglyceride decreased in summer and phospholipid decreased in winter. Exercise diminished the gain in body mass (m) and suppressed seasonal changes in the levels of LDL-C and plasma triglyceride. Seasonal changes in the aorta lipids in this case were similar to those found in non-exercised animals. The values of total energy intake (Q) and of m · Q ^–1 were found to change with season in both non-exercised and exercised rats. Seasonal changes in plasma and in aorta lipids observed in these animals ran in parallel with the respective levels of m · Q ^–1 and/or of Q. The training effect on the lipid values detected in summer and/or in winter was also found to be dependent on the reduction in m · Q ^–1 with exercise. In the non-exercised and in the exercised animals, plasma phospholipid was associated with aorta phospholipid and inversely related to aorta cholesteryl ester and aorta triglyceride. The relationship between these estimations suggests that an increase in the plasma phospholipid in summer would remove non-polar lipids from the walls of the aortae.     

Ca2+ influx induced by store release and cytosolic Ca2+ chelation in HT29 colonic carcinoma cells

Cl^– secretion in HT₂₉ cells is regulated by agonists such as carbachol, neurotensin and adenosine 5-triphosphate (ATP). These agonists induce Ca²⁺ store release as well as Ca²⁺ influx from the extracellular space. The increase in cytosolic Ca²⁺ enhances the Cl^– and K⁺ conductances of these cells. Removal of extracellular Ca²⁺ strongly attenuates the secretory response to the above-mentioned agonists. The present study utilises patch-clamp methods to characterise the Ca²⁺ influx pathway. Inhibitors which have been shown previously to inhibit non-selective cation channels, such as flufenamate (0.1 mmol·l^–1, n=6) and Gd³⁺ (10 mol·l^–1, n=6) inhibited ATP (0.1 mmol·l^–1) induced increases in whole-cell conductance (G _m). When Cl^– and K⁺ currents were inhibited by the presence of Cs₂SO₄ in the patch pipette and gluconate in the bath, ATP (0.1 mmol·l^–1) still induced a significant increase in G _m from 1.2±0.3 nS to 4.7±1 nS (n=24). This suggests that ATP induces a cation influx with a conductance of approximately 3–4 nS. This cation influx was inhibited by flufenamate (0.1 mmol·l^–1, n=6) and Gd³⁺ (10 mol·l^–1, n=9). When Ba²⁺ (5 mmol·l^–1) and 4,4-diisothiocyanatostilbene-2-2-disulphonic acid (DIDS, 0.1 mmol·l^–1) were added to the KCl/K-gluconate pipette solution to inhibit K⁺ and Cl^– currents and the cells were clamped to depolarised voltages, ATP (0.1 mmol·l^–1) reduced the membrane current (I _m) significantly from 86±14 pA to 54±11 pA (n=13), unmasking a cation inward current. In another series, the cation inward current was activated by dialysing the cell with a KCl/K-gluconate solution containing 5–10 mmol·l^–1 1,2-bis-(2-aminoethoxy)ethane-N,N,N,N-tetraacetic acid (EGTA) or 1,2-bis-(2-aminophenoxy) ethane-N,N,N,N-tetraacetic acid (BAPTA). The zero-current membrane voltage (V _m) and I _m (at a clamp voltage of +10 mV) were monitored as a function of time. A new steady-state was reached 30–120 s after membrane rupture. V _m depolarised significantly from –33±2 mV to –12±1 mV, and I _m fell significantly from 17±2 pA to 8.9±1.0 pA (n=71). This negative current, representing a cation inward current, was activated when Ca²⁺ stores were emptied and was reduced significantly (I _m) when Ca²⁺ and/or Na⁺ were removed from the bathing solution: removal of Ca²⁺ in the absence of Na⁺ caused a I _m of 5.0±1.2 pA (n=12); removal of Na⁺ in the absence of Ca²⁺ caused a I _m of 12.8±3.5 pA (n=4). The cation inward current was also reduced significantly by La³⁺, Gd³⁺, and flufenamate. We conclude that store depletion induces a Ca²⁺/Na⁺ influx current in these cells. With 145 mmol·l^–1 Na⁺ and 1 mmol·l^–1 Ca²⁺, both ions contribute to this cation inward current. This current is an important component in the agonist-regulated secretory response.     

Oxygen uptake as related to work rate increment during cycle ergometer exercise

Summary We postulated that the commonly observed constant linear relationship between and work rate during cycle ergometry to exhaustion is fortuitous and not due to an unchanging cost of external work. Therefore we measured continuously in 10 healthy men during such exercise while varying the rate of work incrementation and analyzed by linear regression techniques the relationship between and work rate ( / wr). After excluding the first and last portions of each test we found the mean ±SD of the / wr in ml · min^–1· W^–1 to be 11.2±0.15, 10.2±0.16, and 8.8±0.15 for the 15, 30, and 60 W·min^–1 tests, respectively, expressed as ml·J^–1 the values were 0.187±0.0025, 0.170±0.0027 and 0.147±0.0025. The slopes of the lower halves of the 15 and 30 W·min^–1 tests were 9.9±0.2 ml·min^–1·W^–1 similar to the values for aerobic work reported by others. However the upper halves of the 15, 30, and 60 W·min^–1 tests demonstrated significant differences: 12.4±0.36 vs 10.5±0.31 vs 8.7±0.23 ml·min^–1·W^–1 respectively. We postulate that these systematic differences are due to two opposing influences: 1) the fraction of energy from anaerobic sources is larger in the brief 60 W·min^–1 tests and 2) the increased energy requirement per W of heavy work is evident especially in the long 15 W·min^–1 tests.     

Increase of whole blood lactic acid concentration during exercise as predicted from pH andPCo 2 determinations

In 67 test subjects, an attempt was made to establish whether it is possible to predict the change in the lactic acid concentration of the arterial blood during excercise from the calculated metabolic change in the bicarbonate concentration of the arterial blood during exercise. The changes in the HCO ₃ ^– and the lactic acid concentration averaged —4.15 and 4.41 mEq./l, respectively.It was found possible to predict the measured change in lactic acid concentration from the change in HCO ₃ ^– concentration calculated from the pH and the P Co ₂. A respiratory correction in the calculation ensured the best correlation coefficient (0.81).The regression equation was lactic acid=0.29–0.99 HCO ₃ ^– metabolic.An equally good approximation was attained in calculating the change of lactic acid concentration from the total change in bicarbonate concentration, with application of a simplified respiratory correction: lactic acid=0.33–0.97 (HCO ₃ ^– total –0.18 P Co ₂).The correlation coefficient remained 0.81.With 1 Figure in the TextStudy supported by the European Coal and Steel Community and the Organization for Health Research T.N.O., Netherlands.With the technical assistance of Miss M. L. Hamelink, Mrs. G. de Leeuw-Van Zandwijk and Mr. K. A. Foest.Present address: Dept. of Cardiology.     

The continuous measurement of tubular volume changes in response to step changes in contraluminal osmolality

A new method to measure time dependent (t) volume (V) changes in proximal straight tubules (PST) is described.V is calculated from diameter (d) measurements for which a video camera and an integrating circuit are used. A tubular image of high optical contrast is recorded with the TV camera such that the scan lines run crosswise to the tubule. The video signal is analyzed by a special processor which adds 225 tubular diameters of each TV frame and feeds this analog signal to a pen recorder. The fractional error ind measurements is 10^–3. Diameter changes of less than 0.05 m can be detected, as compared to the usual error of a single measurement of about 0.4 m.P _os ^cb , the osmotic water permeability of the contraluminal cell membrane was measured by setting up osmotic steps across it in less than 0.1 s and following the ensuing d/t. the time delay between solution change and the linear part of the osmotic response was 0.51±0.05 s.P _os ^cb was found to be 50.4 (±8.7)×10^–4 cm³·cm^–2 of basement membrane area ·s^–1·osmolar^–1.     

Volume flow,hydraulic conductivity and electrical properties across bovine tracheal epithelium in vitro: Effect of histamine

Volume flow (J _v), potential difference (), shortcircuit current (i ₀) and electrical resistance (R) were measured simultaneously across bovine tracheal epithelium in vitro. Under basal conditions, with no applied hydrostatic or osmotic pressure gradient (P=0, =0), no spontaneousJ _v was observed. was 31±2 mV (lumen negative),i ₀ 161±8 A cm^–2 andR 202±9 cm²,n=50. When a was applied, by adding 20–80 mM sucrose into the medium bathing either the luminal or the serosal side of the tissue, a linear relationship was found between andJ _v toward the lumen or toward the serosa. The apparent hydraulic conductivity (apparentL _p) was 4.6–4.910^–6 cm s^–1 atm^–1. Histamine 10^–4 M did not induce any spontaneousJ _v under basal conditions and had no effect oni ₀ nor onR. However, histamine caused a 100% increase inJ _v elicited by sucrose gradients. It was concluded that histamine exerts a selective action on the hydraulic conductivity of bovine tracheal epithelium. Experiments using H₁-receptors antagonists (diphenhydramine, dimetindene, chloropyramine) and H₂-antagonists (cimetidine, metiamide) or a H₂-agonist (impromidine) showed that the increase ofL _p induced by histamine was mediated via H₂-receptors.Supported by the Swiss National Foundation (SNF), grant no. 3.5880.79     

Compartmental Analysis of Breathing in the Supine and Prone Positions by Optoelectronic Plethysmography

Optoelectronic plethysmography (OEP) has been shown to be a reliable method for the analysis of chest wall kinematics partitioned into pulmonary rib cage, abdominal rib cage, abdomen, and right and left side in the seated and erect positions. In this paper, we extended the applicability of this method to the supine and prone positions, typically adopted in critically ill patients. For this purpose we have first developed proper geometrical and mathematical models of the chest wall which are able to provide consistent and reliable estimations of total and compartmental volume variations in these positions suitable for clinical settings. Then we compared chest wall (CW) volume changes computed from OEP( V _CW) with lung volume changes measured with a water seal spirometer (SP) ( V _SP)in 10 normal subjects during quiet (QB) and deep (DB) breathing on rigid and soft supports. We found that on a rigid support the average differences between V _SP and V _CW were –4.2% ± 6.2%, –3.0% ± 6.1%, –1.7% ±7.0%, and –4.5% ± 9.8%, respectively, during supine/QB, supine/DB, prone/QB, and prone/DB. On the soft surface we obtained –0.1% ± 6.0%, –1.8% ± 7.8%, 18.0% ± 11.7%, and 10.2% ± 9.6%, respectively. On rigid support and QB, the abdominal compartment contributed most of the V _CW in the supine (63.1% ± 11.4%) and prone (53.5% ± 13.1%) positions. V _CW was equally distributed between right and left sides. In the prone position we found a different chest wall volume distribution between pulmonary and abdominal rib cage (22.1% ± 8.6% and 24.4% ± 6.8, respectively) compared with the supine position (23.3% ± 9.3% and 13.6% ± 3.0%). © 2001 Biomedical Engineering Society. PAC01: 8763Lk, 8719Uv     

Influence of mechanical and metabolic strain on the oxygen consumption slow component during forward pulled running

The possible influence of increased eccentric mechanical work on the increase in oxygen uptake (O₂) after 3 min of running (O₂) was investigated through forward pulled running. Ten subjects ran at individually predetermined constant velocity on a treadmill, while being pulled forward. Ground reaction forces, expired gas and EMGs from leg muscles were collected after 3 min and at the end of the run. O₂ and mechanical work were then calculated. The amplitude of O₂ was 138 (139) ml·min^–1 [mean (SD)]. Increased ventilation explained only 8% of O₂. Stride frequency slightly decreased, inducing a similar decrease in internal work and total mechanical work (all P<0.01), while integrated EMG showed no modifications. It was concluded that O₂ does not come from either an increase in mechanical work production or an increase in muscular activity. O₂ could come from a lower muscle efficiency that could be due to a modification of fibre type recruitment.     

The effect of certain phenothiazine derivatives on respiratory phosphorylation in the cardiac muscle of the rabbit

Summary Phenothiazine derivatives, mepazine and promazine, when added to homogenates of cardiac muscle of the rabbit in a concentration of 0.8·10^–3M, cause a rise in the efficacy of oxidative phosphorylation, increasing the P and the P: O coefficient. In a 1.2·10^–3M, concentration of mepazine and promazine P is reduced, though to a lesser degree than O₂, the P: O coefficient remaining slightly above the normal level.A 0.8·10^–3M phenergan concentration uniformly reduces both respiration and phosphorylation. With a further rise of the phenergan concentration phosphorylation decreases more sharply than respiration. High concentrations of mepazine, phenergan and promazine (1.6·10^–3M) sharply depress phosphocreatine formation and cause a decrease of P: O. The phenothiazine derivatives neither depress creatine kinase nor activate adenosinetriphosphatase.(Presented by Active Member AMN SSSR S. E. Severin) Translated from Byulleten Èksperimental'noi Biologii i Meditsiny Vol. 49, No. 4, pp. 60–63, April, 1960     

Serum carbonic anhydrase III,an enzyme of type I muscle fibres,and the intensity of physical exercise

The effects of 30 min running with stepwise increasing intensity (exhaustive, energy demand approx. 50 100% ofVO_2max), 60 s supramaximal running (anaerobic, 125% ofVO_2max) and 40–60 min low-intensity running (acrobic, 40–60% ofVO_2max) on serum concentration of muscle-derived proteins were studied in 5 male and 5 female elite orienteerers. S-Carbonic anhydrase III (S-CA III) was used as a marker of protein leakage from type I (slow oxidative) muscle fibres and S-myoglobin (S-Mb) as a non-selective (type I+II) muscular marker. The fractional increase in S-CA III (S-Ca III) was 0.37±0.09 (mean±SEM,p<0.001), 0.10±0.05 (N. S.) and 0.46±0.09 (p<0.001) 1 h after exhaustive, anaerobic and aerobic exercise, respectively. The corresponding values for S-Mb were 1.45±0.36 (p<0.001), 0.39±0.13 (p<0.01) and 0.67±0.18 (p<0.001). The value for the S-CA III/S-Mb ratio was 0.68±0.03 after the acrobic exercise, but only 0.25–0.26 (p vs. aerobic exercise <0.001) after the two high-intensity forms of exercise. Since type I fibres of skeletal muscle are known to be responsible for power production during low-intensity exercise, whereas fibres of both type I and type II are active at higher intensities, the S-CA III/S-Mb ratio may depend on the recruitment profile of type I vs. type I+II fibres.     

The anthropometrical and physiological characteristics of elite water polo players

In order to examine the physical and physiological demands of water polo, we assessed the profile of elite water polo players. Nineteen male professional water polo players (age: 25.5±5.0 years, height: 184.5±4.3 cm body mass: 90.7±6.4 kg) underwent body composition assessment by dual-energy X-ray absorptiometry. We also evaluated peak oxygen consumption O_2peak, lactate threshold (LT), energy cost of swimming (C_s), anaerobic capacity and isokinetic shoulder strength. Body fat (%) was 16.8±4.4, lean mass (LM) 75.1±4.9 kg and bone mineral density (BMD) 1.37±0.07 g·cm^–2 . O_2peak was 57.9±7 ml·kg^–1· min^–1 . LT was identified at 3.9±0.7 mmol·l^–1 at a swimming velocity (v) of 1.33±0.05 m·s^–1 with a heart rate of 154±7 bpm, corresponding to an intensity of 83±9 of O_2peak. The average C_s of swimming at the LT was 1.08±0.04 kJ·m^–1 . C_s at LT was correlated to body mass index (BMI) (r=0.22, P=0.04) and to swimming performance at 400 m (r=0.86, P=0.01) and 4×50 m (r=0.84, P<0.01). Internal rotator muscles were stronger compared to the external rotators by a 2:1 ratio. This study provides a quantitative representation of both physical and physiological demands of water polo and proposes a comprehensive battery of tests that can be used for assessing the status of a team.     

Effect of anaerobic and aerobic exercise of equal duration and work expenditure on plasma growth hormone levels

Summary Growth hormone (GH) and lactic acid levels were measured in five normal males before, during and after two different types of exercise of nearly equal total duration and work expenditure. Exercise I (aerobic) consisted of continuous cycling at 100 W for 20 min. Exercise II (anaerobic) was intermittent cycling for one minute at 285 W followed by two minutes of rest, this cycle being repeated seven times. Significant differences (P<0.01) were observed in lactic acid levels at the end of exercise protocols (20 min) between the aerobic (I) and anaerobic (II) exercises (1.96±0.33 mM·l^–1 vs 9.22±0.41 mM·l^–1, respectively). GH levels were higher in anaerobic exercise (II) than in aerobic (I) at the end of the exercise (20 min) (2.65±0.95 g·l^–1 vs 0.8±0.4 g·l^–1;P<0.10) and into the recovery period (30 min) (7.25±6.20 g·l^–1 vs 2.5±2.9 g·l^–1;P<0.05, respectively).