Energy cost of walking and gait instability in healthy 65- and 80-yr-olds.

This study tested whether the lower economy of walking in healthy elderly subjects is due to greater gait instability. We compared the energy cost of walking and gait instability (assessed by stride to stride changes in the stride time) in octogenarians (G80, n = 10), 65-yr-olds (G65, n = 10), and young controls (G25, n = 10) walking on a treadmill at six different speeds. The energy cost of walking was higher for G80 than for G25 across the different walking speeds (P < 0.05). Stride time variability at preferred walking speed was significantly greater in G80 (2.31 +/- 0.68%) and G65 (1.93 +/- 0.39%) compared with G25 (1.40 +/- 0.30%; P < 0.05). There was no significant correlation between gait instability and energy cost of walking at preferred walking speed. These findings demonstrated greater energy expenditure in healthy elderly subjects while walking and increased gait instability. However, no relationship was noted between these two variables. The increase in energy cost is probably multifactorial, and our results suggest that gait instability is probably not the main contributing factor in this population. We thus concluded that other mechanisms, such as the energy expenditure associated with walking movements and related to mechanical work, or neuromuscular factors, are more likely involved in the higher cost of walking in elderly people.     

Immunogenicity of nerve allografts in rats

The state of sensitization of rats after nerve or skin allograft was studied in vitro by using spleen cells or peripheral blood leukocytes (PBL) as responding cells and particulate alloantigen for stimulation, in culture conditions requiring or not supernatant from mixed lymphocytes culture. It is shown that 2-4 weeks after nerve or skin grafting a small number of PBL generates similar cytotoxic lymphocytic responses. However the state of sensitization induced by the nerve allografts is shorter compared to the one exhibited after skin allografts. On the other hand, no significant differences were observed at the level of the humoral response between both groups of grafted rats.     

Hypothalamic Neuroendocrine Circuitry is Programmed by Maternal Obesity: Interaction with Postnatal Nutritional Environment

Objective

Early life nutrition is critical for the development of hypothalamic neurons involved in energy homeostasis. We previously showed that intrauterine and early postnatal overnutrition programmed hypothalamic neurons expressing the appetite stimulator neuropeptide Y (NPY) and suppressor proopiomelanocortin (POMC) in offspring at weaning. However, the long-term effects of such programming and its interactions with post-weaning high-fat-diet (HFD) consumption are unclear.

Research Design and Methods

Female Sprague Dawley rats were exposed to chow or HFD for 5 weeks before mating, throughout gestation and lactation. On postnatal day 1, litters were adjusted to 3/litter to induce postnatal overnutrition (vs. 12 in control). At postnatal day 20, half of the rats from each maternal group were weaned onto chow or HFD for 15 weeks. Hypothalamic appetite regulators, and fuel (glucose and lipid) metabolic markers were measured.

Results

Offspring from obese dams gained more weight than those from lean dams independent of post-weaning diet. Maternal obesity interacted with post-weaning HFD consumption to cause greater levels of hyperphagia, adiposity, hyperlipidemia, and glucose intolerance in offspring. This was linked to increased hypothalamic NPY signaling and leptin resistance in adult offspring. Litter size reduction had a detrimental impact on insulin and adiponectin, while hypothalamic NPY and POMC mRNA expression were suppressed in the face of normal energy intake and weight gain.

Conclusions

Maternal obesity, postnatal litter size reduction and post-weaning HFD consumption caused obesity via different neuroendocrine mechanims. There were strong additive effects of maternal obesity and post-weaning HFD consumption to increase the metabolic disorders in offspring.     

Plasma and lymphocyte Hsp72 responses to exercise in athletes with prior exertional heat illness

We investigated the effect of exercise in the heat on both intracellular and extracellular Hsp72 in athletes with a prior history of exertional heat illness (EHI). Two groups of runners, one consisting of athletes who had a previous history of EHI, and a control group (CON) of similar age (29.7 ± 1.2 and 29.1 ± 2 years CON vs. EHI) and fitness [maximal oxygen consumption $(\dot V{{\text{O}}_2}\hbox{max} )$ 65.7 ± 2 and 64.5 ± 3 ml kg^?1 min^?1 CON vs. EHI] were recruited. Seven subjects in each group ran on a treadmill for 1 h at 72 % $\dot V{{\text{O}}_2}\hbox{max}$ in warm conditions (30 °C, 40 % RH) reaching rectal temperatures of ~39.3 (CON) and ~39.2 °C (EHI). Blood was collected every 10 min during exercise and plasma was analysed for extracellular Hsp72. Intracellular Hsp72 levels were measured in both monocytes and lymphocytes before and immediately after the 60-min run, and then after 1 h recovery at an ambient temperature of 24 °C. Plasma Hsp72 increased from 1.18 ± 0.14 and 0.86 ± 0.08 ng/ml (CON vs. EHI) at rest to 4.56 ± 0.63 and 4.04 ± 0.45 ng/ml (CON vs. EHI, respectively) at the end of exercise (p < 0.001), with no difference between groups. Lymphocyte Hsp72 was lower in the EHI group at 60 min of exercise (p < 0.05), while monocyte Hsp72 was not different between groups. The results of the present study suggest that the plasma Hsp72 response to exercise in athletes with a prior history of EHI remained similar to that of the CON group, while the lymphocyte Hsp72 response was reduced.     

Ultrastructure et constitution des corps nucléaires dans les plasmocytes

Résumé Chez la souris C57 Bl, 2% des sections de noyaux de plasmocytes ganglionnaires contiennent un corps nucléaire, rarement plus. Chez les animaux immunisés par une injection d'hématies hétérologues, le pourcentage de noyaux plasmocytaires contenant un ou plusieurs corps nucléaires augmente jusqu'à 14% du 4ème au 9ème jour qui suivent l'administration de l'antigène. Cette augmentation est parallèle à l'élévation du taux des anticorps sériques. De plus, au même moment, le nombre des noyaux contenant plusieurs corps nucléaires augmente proportionnellement plus que celui des sections n'en contenant qu'un.Les corps nucléaires ont un diamètre moyen de 1,5 . Ils sont principalement formés d'un matériel finement granulaire ou filamenteux dont les éléments constitutifs ont un diamètre de 60 à 70 Å et de granules denses de 250 à 280 Å de diamètre. On en distingue plusieurs types selon la proportion relative et la disposition de ces constituants. Certains contiennent également des formations sphériques plus volumineuses dont le diamètre varie de 1000 à 1400 Å.L'étude ultrastructurale de ces corps après incubation des coupes en présence soit de RNAase soit de DNAase, révèle que les fins granules sont constitués de RNA, tandis que les grains denses représentent du DNA. Les digestions enzymatiques font apparaître une disposition en spirale de ces derniers éléments. Quant aux plus volumineuses formations sphériques, elles subsistent après les deux digestions et apparaissent comme étant en fait des tubes denses à double membrane.L'origine des corps nucléaires est discutée ainsi que la relation entre leur présence et la synthèse des protéines.

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Ultrastructure of the nuclear bodies in the plasma cells

Summary In the C57 Bl mouse, 2% of the sections of plasma cells nuclei from lymphnodes contain one nuclear body (N.B.). The occurrence of two or several bodies per nuclear section is rare. The percentage of plasma cell nuclear sections with one or more nuclear bodies rises up to 14% from the 4th to the 9th day after the injection of heterologous erythrocytes. This increase is parallel to that of blood antibodies. The number of nuclei with several N.B. increases more than that of nuclei with only one.These nuclear bodies have a mean diameter of 1.5 . They are made up of a finely granular or filamentous material (60 to 70 Å in diameter) and of larger dense granules (250 to 280 Å). According to the relative distribution of these constituents, several types of N.B. can be identified. Some of these contain also larger spherical granules with a diameter of about 1000 to 1400 Å.Sections have been incubated with RNAase or DNAase. The fine granules disappear with the former while the dense grains are attacked by the latter enzyme. These digestions show a spiral distribution of the dense grains. The large spherical structures are not modified by these treatments but they are then found to be dense tubes with double membranes.The origin of the nuclear bodies is discussed as well as their relationship to protein synthesis.

     

Etude ultrastructurale de l'origine des plasmocytes ganglionnaires au cours de l'immunisation humorale

Résumé Après une injection unique d'antigène à des souris C 57 B1, la poussée plasmocytaire dans la médullaire ganglionnaire se développe parallèlement à la montée du taux des anticorps circulants du sérum. Ces plasmocytes semblent provenir principalement de la transformation de grandes cellules pyroninophiles. Celles-ci, présentes préalablement dans le cortex, pourraient provenir de la dislocation précoce des centres germinatifs. Elles ne peuvent se transformer en plasmocytes que dans la médullaire. Ces modifications ne pourraient se faire que lorsque la cellule pyroninophile est intégrée au sein d'un ilôt plasmocytaire, c'est-à-dire d'un ilôt dans lequel cette cellule pyroninophile entre étroitement en contact avec un macrophage. A côté de cette origine principale, des plasmocytes peuvent provenir directement de la transformation du lymphoblaste. Enfin, nous avons observé que certaines cellules réticulées se modifient après l'injection de l'antigène. Ces transformations aboutissent à la formation de cellules ayant plusieurs caractères du plasmocyte, sans cependant les présenter tous, d'oú le qualificatif de plasmocytoïde que nous leur avons donné.

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Summary After a single injection of sheep erythrocytes to C 57 Bl mice, the increase in the number of plasma cells in the medullary cords of lymph nodes parallels the humoral antibody titers.The appearance of these plasma cells has been followed ultrastructurally. Most of them arise by modification of the large pyroninophilic cells. These appear at first in the cortex, and could be formed by an early dislocation of the germinal centers. However, the transformation into plasma cells finds place only in the medulla. These changes seem to occur only when pyroninophilic cells are included in a rosette (ilôt plasmocytaire), where they surround a macrophage and develop close connections with it.Other plasma cells may originate directly from lymphoblasts.After the injection of the antigen, some reticular cells are modified into plasmacytoid cells sharing some, but not all, of the morphological characteristics of plasma cells.

     

Precise localization of antigens on follicular dendritic cells

Summary Horse-spleen ferritin or bovine serum albumin conjugated to colloidal gold (BSA-gold) were injected subcutaneously in preimmunized mice. In draining lymph nodes both antigens were located in macrophages or between the cytoplasmic processes of follicular dendritic cells (FDC). Some of the antigens remained trapped on FDC until day 31 after injection. Simultaneous injection of both antigens showed that they were located between the infoldings of the same FDC. These cells are thus able to retain at least two different antigens on their surface. The peculiar arrangement of ferritin between the cytoplasmic infoldings suggests that this antigen is fixed on both cell membranes by specific antibodies. The trapped immune complexes could thus stabilize the FDC membrane system.The antigen retention requires the presence of specific antibodies since BSA-gold or ferritin injected without preimmunization were not found between FDC processes. Nonantigenic materials, such as colloidal gold or carbon particles, are not trapped by FDC, except when injected in large amounts.The antigens were trapped on the surface of FDC, however unfrequently in close contact with lymphocytes. FDC might protect lymphocytes against an excess of immune complexes and act as regulators of contacts between lymphocytes and immune complexes.Abbreviations BSA bovine serum albumin - BSA-gold BSA conjugated to colloidal gold particles - FDC follicular dendritic cells     

Cobalt thiocyanate as a stain for basic proteins and other organic bases on thin sections

Summary Thin sections in mouse mast cells and thymic cells are stained with cobalt thiocyanate a compound known to form insoluble complexes with organic bases. Chromatin, nucleolus, ribosomes and mast cell granules are contrasted. Different blockade reactions and enzymatic digestions indicate the staining corresponds to the basic protein amino-groups.The silver methenamine reaction stains the same cellular structures. However, the specificity control reactions show the staining mainly corresponds to protein sulphydryle groups and in a lesser extent to aldehyde and polyanions.     

Cobalt thiocyanate as a stain for basic proteins and other organic bases on thin sections.

Thin sections in mouse mast cells and thymic cells are stained with cobalt thiocyanate a compound known to form insoluble complexes with organic bases. Chromatin, nucleolus, ribosomes and mast cell granules are contrasted. Different blockade reactions and enzymatic digestions indicate the staining corresponds to the basic protein amino-groups. The silver methenamine reaction stains the same cellular structures. However, the specificity control reactions show the staining mainly corresponds to protein sulphydryle groups and in a lesser extent to aldehyde and polyanions.     

Maternal obesity impairs brain glucose metabolism and neural response to hyperglycemia in male rat offspring

Hypothalamic appetite regulators neuropeptide Y (NPY) and pro‐opiomelanocortin (POMC) are modulated by glucose. This study investigated how maternal obesity disturbs glucose regulation of NPY and POMC, and whether this deregulation is linked to abnormal hypothalamic glucose uptake‐lactate conversion. As post‐natal high‐fat diet (HFD) can exaggerate the effects of maternal obesity, its additional impact was also investigated. Female Sprague Dawley rats were fed a HFD (20 kJ/g) to model maternal obesity. At weaning, male pups were fed chow or HFD. At 9 weeks, in vivo hypothalamic NPY and POMC mRNA responses to acute hyperglycemia were measured; while hypothalami were glucose challenged in vitro to assess glucose uptake‐lactate release and related gene expression. Maternal obesity dampened in vivo hypothalamic NPY response to acute hyperglycemia, and lowered in vitro hypothalamic glucose uptake and lactate release. When challenged with 20 mM glucose, hypothalamic glucose transporter 1, monocarboxylate transporters, lactate dehydrogenase‐b, NPY and POMC mRNA expression were down‐regulated in offspring exposed to maternal obesity. Post‐natal HFD consumption reduced in vitro lactate release and monocarboxylate transporter 2 mRNA, but increased POMC mRNA levels when challenged with 20 mM glucose. Overall, maternal obesity produced stronger effects than post‐natal HFD consumption to impair hypothalamic glucose metabolism. However, they both disturbed NPY response to hyperglycemia, potentially leading to hyperphagia.