Search PubMed⌕ Search

Biomedical subjects

U Schreiber

Publications and source records attributed to U Schreiber.

At least 37 records · Page 2Linked to original sources

Two fundamentally different types of variable chlorophyll fluorescence in vivo.

Upon onset of saturating continuous light only the first part of the observed polyphasic fluorescence rise follows Q(A) reduction (photochemical phase), whereas the remaining part (thermal phases) is kinetically limited by relatively slow reactions with light saturated half-times in the order of 10-50 ms. A simple hypothesis is presented for the interpretation of these fundamentally different types of variable fluorescence. The hypothesis, which is based on the reversible radical pair model of PSII, assumes stimulation of both prompt and recombination fluorescence upon Q(A) reduction, with only recombination fluorescence being in competition with nonradiative energy loss processes at the reaction centers. It is proposed that changes in the rate constants of these processes modulate the yield of recombination fluorescence in closed centers, thus causing large variations in the maximal fluorescence yield and also giving rise to the 'thermal phases'. This hypothesis can reconcile numerous experimental findings which so far have seemed difficult to interpret.

Chlorophyll↗

Study of heme Fe(III) ligated by OH- in cytochrome b-559 and its low temperature photochemistry in intact chloroplasts.

EPR properties of Cyt b-559 have been investigated in intact chloroplasts that are functionally competent in O2 evolution and in CO2 fixation. After chemical oxidation of Cyt b-559 by 10 mM 2,3-dicyano, 4,5-dichloro-p-benzoquinone (DDQ) the major part of Cyt b-559 is found to be present in the high spin Fe(III) form. Only a small fraction of low spin heme Fe(III) (less than 5%) was formed by chemical or light-induced oxidation. This fraction increased during aging of intact chloroplasts. A comparison with the EPR signal of Fe(III) in myoglobin (Mb) reveals that the structure of the high spin signal in intact chloroplasts is indicative for the presence of an axial OH- ligand at the heme Fe(III). This type of ligation comprised a considerable part (approximately 40%) of the total Cyt b-559 content. Removal of the Mn-cluster caused a change of the EPR parameters of OH- ligation. When in intact chloroplasts the heme Fe is chemically oxidized to Fe(III) ligated by OH-, this OH- ligation disappeared after a subsequent illumination at 80K by red light. Upon illumination at 140K this disappearance was accompanied by the formation of a high spin Fe(III) that is not ligated by OH-. These results are discussed in terms of removal of OH- from Fe(III) caused by structural changes or photooxidation at a complex of Cyt b-559 that could possibly also comprise the Mn-cluster. This photooxidation is assumed to be accompanied by the formation of a bound OH. radical. The possibility is discussed that this process is related to photosynthetic water oxidation.

Benzoquinones↗

Spectral and thermodynamic properties of the two hemes of the D1D2cytochrome b-559 complex of spinach.

In agreement with previous work [Shuvalov, Heber and Schreiber (1988) FEBS Lett. 258, 27-31] two hemes (low potential (LP) and extra low potential (XLP)) per two pheophytins were found in isolated D1D2Cyt b-559 complexes. Reductive and oxidative redox titrations demonstrate that the Em of the LP form is at about +150 mV. It is independent of pH between pH 7.2 and 9.4. The XLP heme is autoxidizable at pH 7.2 and displays, at this pH, an Em of -45 mV. Both the LP and XLP hemes show absorption peaks at 559 nm. They are proposed to have bis-histidine ligation of the heme iron. At pH 9.4, the XLP heme splits into two forms. One of them has an Em of +40 mV, and absorption peaks at 559 nm showing the bis-histidine ligation. The other displays an Em of -220 mV and the peak is shifted to 562 nm. This last form is proposed to be due to the incorporation of OH- which occupies the 6th coordination position of the heme Fe(III) at high pH. The pK value for the conversion of the XLP heme is close to 7.7. In a structure simulation of the alpha-helices of alpha- and beta-polypeptide, the beta-polypeptide, but not the alpha-polypeptide, reveals a distance between the histidine N and the heme Fe which permits stable N-Fe coordination. In the alpha-polypeptide, OH- can be incorporated between N and Fe. The functional role of the two hemes of cyt b-559 is briefly discussed with respect to water oxidation and cyclic electron transfer.

Chlorophyll↗

Selective interaction of valinomycin/K+ with the cytochrome bf complex of chloroplasts. Synergistic effect with MOA stilbene on extent of cytochrome b563 reduction in continuous light.

Valinomycin/K+ is shown to selectively interact at sub-micromolar concentrations with the cytochrome bf complex in thylakoid membranes, inducing a red shift of the ferrohaem b absorbance alpha-band, a slow down of post-illumination b-reoxidation and a corresponding increase of b-reduction level in continuous light. These effects of valinomycin/K+ are not related to its field dissipating action, as they are not affected by nonactin. Presence of K+ is required. Phenomenologically the valinomycin/K+ effects are similar to those caused by 10 times higher MOA stilbene nonactin. Presence of K+ is required. Phenomenologically the valinomycin/K+ effects are similar to those caused by 10 times higher MOA stilbene concentrations. However, synergism is observed between the two inhibitors, suggesting different modes of action. When both inhibitors are combined more than one haem b can be reduced by illumination.

Chloroplasts↗

[Insulin-sulfonylurea combination therapy in secondary therapy failure with sulfonylurea compounds. Randomized study between evening and morning intermediary insulin administration using the Novo Pen semi-automatic insulin injector].

In 28 type II diabetics with secondary failure of sulfonylurea treatment, the efficacy and safety of combined therapy with insulin and glibenclamide were investigated. Patients were randomized in two groups and treated for 16 weeks either with insulin Novo Protaphan HM Penfill (100 IU/ml "bed time") and 10 mg of glibenclamide in the morning (group A), or with insulin Novo Actraphan HM Penfill 100 IU/ml in the morning combined with two 5 mg doses of glibenclamide at lunchtime and in the evening (group B). Subsequently a dropout trial of sulfonylurea was performed in half of the patients. Mean blood glucose levels were lowered in the whole group of patients from 13.5 +/- 1.8 mmol/l to 8.8 +/- 2.3 mmol/l after 8 weeks and 8.7 +/- 1.8 mmol/l after 16 weeks, and the HbAlc from 10.1 +/- 1.2% to 8.4 +/- 1.0% and 7.8 +/- 1.0% respectively. After a glibenclamide dropout period of one or two weeks in 14 of the patients, the mean blood glucose level rose significantly by 2.8 +/- 2.6 mmol/l. Only 2 patients did not show this increase. The mean insulin consumption was 13 +/- 3 IU after 8 weeks and 14 +/- 5 IU after 16 weeks respectively, and the incidence of hypoglycemia one in 12 weeks of treatment. The combination of glibenclamide and insulin (administered with the Novo Pen injector) is a safe and effective form of therapy in secondary failure of sulfonylurea, and is well accepted due to the mild start into insulin therapy.

Adult↗

Photosynthesis and Chlorophyll Fluorescence Characteristics in Relationship to Changes in Pigment and Element Composition of Leaves of Platanus occidentalis L. during Autumnal Leaf Senescence.

The loss of chlorophyll and total leaf nitrogen during autumnal senescence of leaves from the deciduous tree Platanus occidentalis L. was accompanied by a marked decline in the photosynthetic capacity of O(2) evolution on a leaf area basis. When expressed on a chlorophyll basis, however, the capacity for light-and CO(2)-saturated O(2) evolution did not decline, but rather increased as leaf chlorophyll content decreased. The photon yield of O(2) evolution in white light (400-700 nanometers) declined markedly with decreases in leaf chlorophyll content below 150 milligrams of chlorophyll per square meter on both an incident and an absorbed basis, due largely to the absorption of light by nonphotosynthetic pigments which were not degraded as rapidly as the chlorophylls. Photon yields measured in, and corrected for the absorptance of, red light (630-700 nanometers) exhibited little change with the loss of chlorophyll. Furthermore, PSII photochemical efficiency, as determined from chlorophyll fluorescence, remained high, and the chlorophyll a/b ratio exhibited no decline except in leaves with extremely low chlorophyll contents. These data indicate that the efficiency for photochemical energy conversion of the remaining functional components was maintained at a high level during the natural course of autumnal senescence, and are consistent with previous studies which have characterized leaf senescence as being a controlled process. The loss of chlorophyll during senescence was also accompanied by a decline in fluorescence emanating from PSI, whereas there was little change in PSII fluorescence (measured at 77 Kelvin), presumably due to decreased reabsorption of PSII fluorescence by chlorophyll. Nitrogen was the only element examined to exhibit a decline with senescence on a dry weight basis. However, on a leaf area basis, all elements (C, Ca, K, Mg, N, P, S) declined in senescent leaves, although the contents of sulfur and calcium, which are not easily retranslocated, decreased to the smallest extent.

Journal Article↗

[Structure of the wall of the gastrointestinal tract: a comparative sonographic-morphologic study].

High frequency ultrasound can resolve the structure of the wall of the gastro-intestinal tract into three highly echogenic lines with poorly echogenic zones between them. Sequential removal of layers of the walls of fresh specimens of the gastro-intestinal tract showed the following correlation between the sonographic and histological findings: the innermost and outermost highly echogenic lines correspond to incident and exit echoes. The middle line corresponds with the sub-mucosa and the junctional zones of the mucosa/muscularis mucosa and sub-mucosa/muscularis propria. The intervening low echo lines correspond with the mucosa and muscularis propria.

Animals↗

Circadian variations of urine excretion and adrenocortical function in different states of hydration in man.

On 3 different days, the circadian rhythms of urinary volume and cortisol excretion were measured under different conditions of water supply in healthy male subjects. The water intake was systematically varied (100, 350, and 600 ml/3 hr of tap water) starting 6 hr before the beginning of the measurements, which were carried out under constant bed rest in a climatic chamber. Every 3 hr, a standardized low-protein meal was administered. The daily courses of cortisol excretion showed an increase of the mesor, which was proportional to the amount of water intake. The absolute amplitude was significantly higher when 600 ml/3 hr was taken. The circadian acrophase was shifted in advance, and the slope of the curves after the nightly minimum was significantly increased in the experiments with 350 and 600 ml/3 hr fluid intake. The urinary volume showed analogous modifications. These results are interpreted as a nonspecific activation of the adrenal cortex and a circadian variation of the sensitivity of renal regulation of the water balance.

Adrenal Cortex↗

Effects of BAY l 5240, a fixed combination of low dose nifedipine and acebutolol on hypertension: comparison with standard dose nifedipine.

116 patients from 4 clinics participated in a double blind study to assess the efficacy of (BAY l 5240), a nifedipine-acebutolol fixed combination (10 mg + 100 mg), as compared to nifedipine 20 mg in essential hypertension. During the 10 week study, the mean recumbent blood pressure decreased 1 to 3 h after treatment from 175.5/105.2 to 148.3/88.0 mmHg in the BAY l 5240 group and from 174.3/102.9 to 150.3/86.5 mmHg in the nifedipine group. The results also showed a comparable decrease in the mean systolic (SBP) and diastolic (DBP) blood pressures before treatment (24 h after last tablet) and after physical exertion before and after either drug given for 4 weeks. Doubling of the dose for 4 additional weeks produced a moderate and similar additional decrease in blood pressure. The results show the possibility of treating essential hypertension with a low dose of a beta-adrenergic blocking agent in combination with 10 mg nifedipine. Both regimens were well tolerated. One patient in the BAY l 5240 group and 2 in the nifedipine group, all treated by the same investigator, were withdrawn from the study because of headache during the nifedipine pre-period.

Acebutolol↗

Effects of a fixed combination of low dose nifedipine and acebutolol on essential hypertension: comparison with standard dose acebutolol.

114 patients from four clinics participated in a double blind study designed to assess the efficacy of a nifedipine-acebutolol fixed combination -10 mg + 100 mg - as compared with acebutolol -200 mg- in essential hypertension. During the ten week study the mean blood pressure readings (s.d.) 1-3 h after treatment decreased from 179.2/104.8 (10.2/6.2) to 150.3/87.7 (9.8/7.7) in the combination group and from 181.7/106.5 (14.4/7.0) to 150.4/89.0 (15.0/10.4) in the acebutolol group. The mean systolic and diastolic blood pressures were also decreased after exertion (load) and 24 hours after treatment at the end of the 6th week of the study. A doubling of the dose from week 7 to 10 did not change these figures. These results reveal the possibility of treating essential hypertension with a low dose of beta-adrenergic blocking agents in combination with 10 mg nifedipine. Both drugs were well tolerated. 3 patients (5%) in the combination group and 3 patients in the acebutolol group were withdrawn from the study because of headache and dizziness.

Acebutolol↗

Correlation between membrane-localized protons and flash-driven ATP formation in chloroplast thylakoids.

Flash-driven ATP formation by spinach chloroplast thylakoids, using the luciferin luminescence assay to detect ATP formed in single turnover flashes, was studied under conditions where a membrane protein amine buffering pool was either protonated or deprotonated before the beginning of the flash trains. The flash number for the onset of ATP formation was delayed by about 10 flashes (from 15 to about 25) when the amine pool was deprotonated as compared to the protonated state. The delay was substantially reversed again by reprotonating the pool upon application of 20-30 single-turnover flashes and 8 min of dark before addition of ADP, Pi, and the luciferin system. In the case of deprotonation by desaspidin, the uncoupler was removed by binding to BSA before the reprotonating flashes were given. Reprotonation was carried out before addition of ADP and Pi, to avoid a possible interference by the ATP-ase, which can energize the system by pumping protons. The reprotonated state, as indicated by an onset lag of about 15 flashes rather than 25 for the deprotonated state, was stable in the dark over extended dark times. The number of protons released by 10 flashes is approximately 30 nmol H+ (mg chl)-1, an amount similar to the size of the reversibly protonated amine group buffering pool. The data are consistent with the hypothesis that the amine buffering groups must be in the protonated state before any protons proceed to the coupling complex and energize ATP formation. Other work has suggested that the amine buffering pool is sequestered within membrane proteins rather than being exposed directly to the inner aqueous bulk phase. Therefore, it is possible that the sequestered amine group array may provide localized association-dissociation sites for proton movement to the coupling complex.

Adenosine Triphosphate↗

Light-Induced Proton Gradient Formation in Intact Cells of Dunaliella salina.

A light-induced proton gradient (DeltapH) increase as exhibited by an increase of 9-aminoacridine fluorescence quenching is demonstrated between the external medium and the interior of the halophytic green alga Dunaliella salina. The formation and maintenance of the DeltapH is sensitive to electron transport inhibitors and to uncouplers. It is inhibited by p-chloromercuribenzenesulfonic acid (50% inhibition at 3 micromolar), which does not affect photosynthetic O(2) evolution. It is concluded that the observed DeltapH is located across the plasmalemma or the chloroplast envelope. The formation and maintenance of the light-induced proton gradient requires the presence of Na(+). Substitution of NaCl by KCl or glycerol results in inhibition of the DeltapH formation. The proton gradient is also sensitive to ATPase and energy transfer inhibitors. It is suggested that a Na(+)/H(+) pump mechanism may be involved in the formation of the proton gradient in intact Dunaliella cells.

Journal Article↗

Reversible uncoupling of energy transfer between phycobilins and chlorophyll in Anacystis nidulans: light stimulation of cold-induced phycobilisome detachment.

Phycobilin fluorescence of Anacystis nidulans grown at 28 degrees C increases substantially upon cooling below 10 degrees C. A maximal increase is found around -5 degrees C and amounts to 300%, with almost complete reversibility upon re-warming. Illumination with actinic light leads to considerable stimulation of the cold-induced phycobilin fluorescence increase. Analysis of the light stimulation phenomenon reveals: (1) Actinic illumination shifts the fluorescence-temperature characteristic by about 3 degrees C upwards on the T-axis. At temperatures below 5 degrees C the light stimulating effect becomes smaller again and fluorescence-temperature characteristics measured at high and low light intensity converge around -5 degrees C. (2) In the 13-8 degrees C region a large (up to 100%) light-induced phycobilin fluorescence increase is observed, while only negligible changes occur in the dark. (3) 3-(3,4-Dichlorophenyl)-1,1-dimethyl urea (DCMU) as well as uncouplers inhibit the light stimulation, which hence depends on coupled electron transport. In agreement with previous work (Schreiber, U. (1979) FEBS Lett. 107, 4-9) it is concluded that illumination enhances cold-induced phycobilisome detachment by increasing the net negative charge at the outer surface of the thylakoid membrane. The possible role of a fluid leads to ordered transition of membrane lipids (Murata, N. and Fork, D.C. (1975) Plant Physiol. 56, 791-796) is discussed.

Chlorophyll↗

Salt-Induced Metabolic Changes in Dunaliella salina.

An increase of medium NaCl concentration induces Dunaliella cells to evolve O(2) photosynthetically even in the absence of CO(2). This NaCl-induced O(2) evolution may reflect the induced conversion of reserve carbohydrate to glycerol. The quantum yield for the NaCl-induced O(2) evolution, in the absence of CO(2), is 1.5-fold higher than that obtained for CO(2) fixation. Since the synthesis of glycerol from reserve carbohydrate in the absence of CO(2) requires only 0.5 ATP/NADPH, whereas photosynthesis requires at least 1.3 ATP/NADPH, it is concluded that the ATP/2e(-) ratio coupled to NADP reduction in Dunaliella is lower than required for CO(2) fixation.

Journal Article↗

The kinetic relationship between the C-550 absorbance change, the reduction of Q(delta A320) and the variable fluorescence yield change in chloroplasts at room temperature.

The light minus dark difference spectrum and the kinetics of the indicator pigment C-550 have been measured at room temperature in isolate, envelope-free chloroplasts in the presence of 3-(3' ,4'-dichlorophenyl)-1,1-dimethylurea (DCMU). The C-550 spectrum indicates a band shift with peaks at 540 and 550 nm and has an isobestic point at 545 nm. On the assumption of 400 chlorophyll molecules per electron transfer chain the differentaial extinction coefficient delta epsilon (540-550) is calculated to be approximately 5 mM-1 . CM-1. The kinetics of the C-550 absorbance change, occurring upin the onset of continuous illumination, are shown to be biphasic and strictly correlated with the kinetics of the complementary area measured from the fluorescence induction curve under identical cinditions and with those of the absorbance increase at 320 nm due to photoreduction of Q. The lighted-induced change in these three parameters can be described as a function of the variable fluorescence yield change occurring under the same conditions. Such functions are non-linear and reveal a heterogeneous dependence of the variable fluorescence yield on the fraction of closed System II reaction centers. It is concluded that for every molecule of the primary electron acceptor Q of Photosystem II that is photochemically reduced there corresponds an equivalent change in the absorbance of the indicator pigment C-550 and in the size of the complementary area. Ths, C-550 and area are two valid parameters for monitoring the primary photochemical activity of System II at the room temperature.

Chloroplasts↗