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L Pénzes

Publications and source records attributed to L Pénzes.

At least 19 recordsLinked to original sources

Relationship between a long-term treatment of 2-mercaptoethanol and protein metabolism in the ageing rat.

Female RLEF1/Lati rats were chronically treated with 2-mercaptoethanol in a dose of 13 micrograms.100 g bw-1.day-1 dissolved in drinking water. During a 48-h experiment 15N-labelled glycine was given orally in a dose of 5 mg 15N.kg bw-1 and urine samples were collected and analysed by an emission spectrometric isotope method. Protein synthesis and nitrogen excretion rate constants were calculated according to the three-pool model, and 3-methylhistidine excretion rates were also determined. 2-Mercaptoethanol appears to influence protein metabolism; however, the slower rates of protein synthesis proved to be apparent in almost all groups of treated rats. Protein synthesis and nitrogen excretion rate constants have exceptionally high values in 2-year-old rats, possibly explained by the occurrence of hypercompensation mechanisms in old age. These were reflected by the excretion rates of 3-methylhistidine which were reduced as a result of sulphhydryl group interactions in age-dependent cellular metabolic changes.

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Effect of cigarette smoke and 2-mercaptoethanol administration on age-related alterations and immunological parameters.

In old CBA/Ca mice the effect of cigarette smoke was compared with that of 2-mercaptoethanol (2-ME) treatment. It could be stated that spontaneous death was more frequent in animals kept in cigarette smoke than in the control animals. Prevalence of hepatocellular carcinoma was higher in animals kept in cigarette smoke than in the controls. After 2-ME treatment the occurrence of hepatocellular carcinoma was significantly lower and animals without disorders were more frequent than in smokers. Body weights were lower in animals kept in cigarette smoke and differences in organ indices could be observed, too. Immunological changes were also demonstrated: in mice kept in cigarette smoke the reactivity against a foreign antigen such as sheep erythrocytes (SRBC) was lower, while after 2-ME treatment it was higher than in their controls using direct plaque formation technique. The ratio of normal reactivity (against SRBC) and autoreactivity (against mouse erythrocytes) showed a decrease in smoker animals, and an increase in the 2-ME-treated ones. The experiments showed a deleterious effect of cigarette smoke and a beneficial effect of 2-ME on age-related alterations.

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Effect of an antioxidant compound (2-mercaptoethanol) on the nerve terminals of the aging small intestine.

The effect of 2-mercaptoethanol (2-ME) treatment on the nerve elements of the small intestine has been investigated in old mice. In control animals only a few synapses and a very small number of vesicles were found in the nerve terminals. Some of the nerve fibers were observed to be degenerating. After drinking 2-ME daily for 17 months, both the number of synapses and vesicles within the nerve terminals increased. No degenerated fibers were observed. It is assumed that 2-ME has a beneficial influence on the peripheral intestinal nervous system increasing the number of synapses and the vesicle population in the nerve terminals.

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Effect of 2-mercapto-ethanol on some brain biochemical characteristics and behavioural changes in the ageing CBA/Ca mice.

Male CBA/Ca inbred mice were treated with a dose of 8 micrograms 2-mercapto-ethanol per animal per day in the drinking water from the age of 5 months onwards up to the age of 24 months. Dopamine release was greatly decreased in old animals in contrast to the elevation of dopamine release in the treated mice. Similarly, an elevated malondialdehyde content in brain homogenates was also observed in the aged treated animals compared with their controls. No essential differences were observed in locomotor activity and learning between treated an control mice.

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Effect of 2-mercaptoethanol on posthypoxic and age-related biochemical and behavioural changes in mice and rats.

2-Mercaptoethanol (2-ME) has a beneficial effect on the mean life span of laboratory rodents. This paper deals with the effects of 2-ME on changes of dopamine release from brain slices of old aged or hypoxia exposed mice and rats. The results were compared with data which reflect spontaneous peroxidation of brain lipid constituents. In addition, adequate behavioural properties were studied. Long-term 2-ME treatment for months abolishes the age-related decrease of transmitter release and prevents changes in malondialdehyde formation. If age-dependent release failure is already established, then neither single high doses of 2-ME nor repeated treatment for 3 weeks are effective. Posthypoxic release inhibition is prevented by a 2-ME pretreatment for 3 weeks but not by an acute single application even at high dosages. The preventive effect of 2-ME is a mediated one rather than an immediate direct action. Age-related behavioural deficits, such as locomotor activity, habituation performance and learning ability, do not reflect any effect of 2-ME long-term treatment.

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Effect of 2-mercaptoethanol on some metabolic indices of ageing of CBA/Ca inbred mice.

It has been shown in several studies that 2-mercaptoethanol (2-ME) improves the life span and aspects of life performance of laboratory animals. To obtain further details on the beneficial effects of 2-ME, a long-term study has been performed on male CBA/Ca inbred mice treated with this antioxidant. Four month-old mice were each given 4 micrograms of 2-ME in physiological saline via intraperitoneal (i.p.) injection 3 x per week. Measurements were made of the following: cold tolerance (heat performance), apparent total body protein turnover (T1/2), changes in the major lipid and fatty acid compositions of the liver, superoxide dismutase activity and formation of malondialdehyde and observations on a range of pathological changes. It was found that the basal rectal temperatures of the treated mice were higher and in the oldest group, heat performance capacity was better than those of the controls. After about 1 year of age the apparent biological half-life time of total body protein (T1/2) was observed to be shorter in the treated mice. Significant increases were observed to occur in the proportions of the polyunsaturated fatty acids in the lipids of the liver in the mice injected with 2-ME. Although no differences were observed in the superoxide dismutase activities, malondialdehyde concentrations in the livers of the experimental mice were significantly increased. Autopsy data showed that Dunn-sarcomas associated with amyloidoses occurred more frequently in the untreated mice.

Aging↗

Density of substance P, vasoactive intestinal polypeptide and somatostatin-containing nerve fibers in the ageing small intestine of the rats.

Immunoelectron microscopic investigations were carried out to study the substance P, vasoactive intestinal polypeptide (VIP) and somatostatin immunoreactive nerve elements in the wall of the small intestine. In young and old animals a large number of immunoreactive nerve fibers were found in all layers of the small intestine. They were observed closely to the epithelial cells, to the blood vessel basement membrane and to the smooth muscle cells and in some cases they were observed in a synapse with other unlabelled nerve fibers. On the other hand, in the senile animals very few immunoreactive nerve fibers were observed, calculated for a 100 micron2 tissue area. In the senile animals the overall number of nerve fibers was decreased in comparison to the young and old animals and most of them were in degeneration. This change could be the cause of the changes in the senescence-related epithelial transport processes and furthermore, of the modifications of the overall intestinal motility of the gastrointestinal tract, resulting in the age-dependent transit rates.

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Biological changes and diseases in aged CBA/Ca mice.

Cold adaptation, apparent protein metabolism, life span, body and organ weights, organ indices, mitochondrial changes in the lymphocytes, and frequency of diseases were examined in 661 (untreated) inbred CBA/Ca male mice. The rectal temperature proved to be lower in aged mice, i.e. the rectal temperature of old animals immediately after cold exposure was more distinctly decreased than that of young ones. The apparent protein metabolism measured by 75Se-selenomethionine turnover showed that biological half-life (T 1/2) values in the aged are almost linearly elevated. In very old animals the values are decreased. Body weight decreased significantly and continuously, spleen and liver indices decreased and heart index increased with age in healthy animals. The number of diseased animals increased with age peaking at the age of 751-900 days. After 900 days the number of diseased animals decreased. The most frequent diseases in the old animals are: hepatocellular carcinoma, amyloidosis and pulmonary adenocarcinoma. The mitochondria of spleen lymphocytes showed degenerative changes not associated with diseases, thus they can be considered as age-related biological changes.

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Changes in the intestinal microvillous surface area during reproduction and ageing in the female rat.

A morphometric study has been undertaken of the changes that occur in the microvillous surface area of young, pregnant, lactating, old and senescent rats. It has been shown that the microvilli are organelles with a quite stable conformation and that they exhibit no large scale dimensional changes throughout almost the entire life span. Lactation, however, does induce an apparent increase in microvillous surface area which may be associated with the significant changes which occur to the structure of the villus during reproduction in the rat.

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Intestinal response in aging: changes in reserve capacity.

In contrast to the cardiovascular system, the gastrointestinal tract in old age does not reveal the marked structural and functional deteriorations that might be expected to arise from the body's aging process. Besides preserving an active mass of functional tissue, the intestinal regulatory mechanisms show a precise and functional response to the changing circumstances of aging. With regard to the aging processes, therefore, the relative physiological stability of the gastrointestinal system is very important. A possible cause of the maintenance of its functional capacity may be the processes involved in the cellular aging and rapid turnover of the gastrointestinal epithelium. This part of the gut remains practically unchanged and may continue its growth processes almost up to the point of death. Thus, intestinal functions do not seem to deteriorate even in late age. Kinetic studies indicate that the intestinal response in senescense to secure normal absorption processes occurs through an adaptation of transfer (carrier mediated) mechanisms. Such model studies have suggested that with age the affinity of the intestinal carrier mechanisms for the absorption of glucose and neutral amino acids are diminished. Appropriate changes in absorption occur i.e. in the young a faster rate of absorption is achieved at low luminal concentration than in the old. The amounts and activities of many essential intestinal enzymes have been observed to be reduced with age. This too may lead to a slower rate of absorption. In old age therefore it is the rate of intestinal absorption that undergoes a significant change rather than an overall deterioration in absorptive ability. Our present knowledge indicates that there are at least two important regulatory mechanisms that enable the aged gastrointestinal tract to adapt itself to its altered functional capacity. On the one hand, the response of the intestinal epithelium mediated by the various rapid repair processes for the uptake of substances needed by the organism, and, on the other hand, the existence of the current load in the luminal environment controlling the intestinal metabolism and homeostasis in a normal way during aging. An analysis of the close relationship that exists between structure and function in the gastrointestinal tract during aging, in particular the reasons for the observed alterations of the absorptive surfaces, will undoubtedly be useful in the practical elucidation of such problems as mucosal injuries, resection and malabsorption therapy.

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Long-term observations on the effect of polyadenylic acid in mice of different ages.

In order to better life performance, polyadenylic acid (poly (A) ) was given intraperitoneally to CBA/Ca mice for almost a two-year period. This substance, as one of the components of double-stranded polynucleotides (like poly A:U), is known to improve some immune responses of the aging organism. Five approaches (changes in body-weight, adaptation to cold stress, biological half-life of body proteins, mortality and pathology) were applied to test the effects of this substance on life performance. It was found that the beneficial effects of double-stranded polynucleotides cannot be mimicked by polyadenylic acid only, despite its anti-senescence effect, namely, it accelerates the apparent protein turnover, cf., biological half-life. Polyadenylic acid shortens life-expectancy (because of the higher mortality rate of mice). Possible mechanisms of these actions are discussed.

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Effect of aminoethyl-isothiuronium (AET) treatment on intestinal cell proliferation during ageing.

To establish whether aminoethyl-isothiuronium X bromide X hydrobromide (AET) treatment influenced intestinal cell proliferation during ageing, juvenile and aged female rats were treated with AET for a period of 20 days. Subsequent incorporation of 3H-thymidine was studied in the epithelial cells of the duodenal and jejunal crypts. It was found that after AET administration the major changes occurred in the duodenum, i.e. the number of the villous epithelial columnar cells were found to be elevated during senescence with a markedly higher level of mitotic numbers in the crypts. Changes were less in the ageing jejunum, here neither the cells nor the number of mitoses were as altered as those of the duodenal region. In general, the labelling indices of crypt cells increased in young ages after AET treatment. The findings can be explained by the role of AET with respect to nuclear metabolism.

Aging↗

[On the interrelationship between lifespan, constitution and information (Parts 1 and 2) (author's transl)].

The authors have tried to summarize the biophysical causes, laws and consequences of the processes of ageing. After surveying the development which Man's life span and senescence have undergone in the course of evolution as well as the underlying causes, they demonstrate the influence which the size of the brain has on the life span. A correlation can be shown to exist between brain weight, body weight, metabolic rate, body temperature and life span. Furthermore, an interrelationship between the amount of information available and ageing was not only observed at the cellular level, but also studied in more complex structures. The authors point that that the increase in entropy is linked with the ageing process and that the differences in the capacity of the nervous system (which are equivalent to a given difference in entropy) are accompanied by the same alteration of the live span as if this difference in entropy resulted from deviations in the metabolic processes.

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Intestinal absorption in the aged.

The difficulties of differentiating functional disorders from organic diseases of the intestinal tract in old age are well known. It is also known that the age-related structural changes of the digestive tract are inconclusive of any functional disorder. This has raised the question whether the process of aging is bound to affect the absorption of d-glucose and the amino acids (gly, ala, val, thr, leu, phe, try, pro, his, lys and arg). The results of the present rat experiments, which have been undertaken under a kinetic approach, indicate that the intestinal carrier affinity to the molecules available for transport declines with aging. This implicates that in the young animal the transport of the absorbed molecules from the intestinal lumen at low (initial) concentrations proceeds at a higher rate than it does in the old animal. The reverse was found to be the case for the basic amino acids.

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[Glucose absorption from the small intestine in rats of different ages (authors transl)].

Glucose absorption from the ageing rat's small intestine was studied "in vivo" using the recirculation-perfusion method of Sheff and Smyth. Different initial concentrations were used and animals of various ages (6 mo., 12 mo. and more than 27 mo. old) tested for their glucose uptake from the total small intestine (including duodenum) in the course of a twenty-minute period. Glucose was estimated by the modified o-toluidine method of Hultman. The (reciprocal) absorption data, reduced on dried intestine weight units were plotted by the Lineweaver -- Burk (regression) equations and the Km and Vmax indices derived. The results show that there is an apparent increase of the Km value in case of the old rats. Regarding the Km as an apparent affinity constant of the glucose for the carrier transport, ageing induces a considerable loss in affinity and a concomitant increase of the maximum absorptive capacity (Vmax) possible by the transfer capacity of the ageing small gut. The interpretation of the data suggest that the role of the probable age-dependent changes of diffusion-components cannot be ruled out.

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