Effect of heat and cold factors on amylolytic and invertase activity of the small intestine in growing rats

Acute experiments on young rats showed that exposure to heat (40–41°C) and cold (5–6°C) and injections of ACTH (4 units/100 g body weight per injection) during the first week of life led to a sharp decrease in total amylolytic and invertase activity of homogenates and everted segments of the small intestine of the animals. The inhibition of intestinal function continued throughout the next 2 weeks of life.Laboratory of the Physiology of Digestion, Institute of Physiology, Academy of Sciences of the Uzbek SSR, Tashkent. (Presented by Academician V. N. Chernigovskii.) Translated from Byulleten' Éksperimental'noi Biologii i Meditsiny, Vol. 82, No. 10, pp. 1213–1215, October, 1976.     

Antigenic properties of ovalbumin following heat denaturation at different temperatures: Comparison with enzymatic Denaturation

Eighteen monoclonal antibodies (MAbs) raised from mice which were immunized with either native ovalbumin (NOA) or ovalbumin which had been heat denatured at 100°C, (HDOA) were used to study antigenic modifications induced by either heat or subtilisin treatment. Using enzyme immunoassays (EIA) we have defined three major groups of antigenic sites: Group I thermolabile native epitopes; Group II relatively thermostable native epitopes; Group III epitopes specific to heat‐denatured ovalbumin. Heatdenatured ovalbumin can be separated into monomers and polymers which constitute 1% and 99% of the molecules respectively. Whereas MAbs belonging to Groups I and II bound to the monomeric form (mHDOA), MAbs belonging to Group III only bound to the polymeric form (pHDOA). Plakalbumin (PK) behaved similarly to pHDOA since it was recognized by many MAbs from Group III and a few from Group II. Nevertheless, PK remained as a monomeric molecule, whereas heat‐denatured ovalbumin existed mainly as polymeric aggregates. The epitopes present on ovalbumin after different heating procedures (time/temperature) were found to be stable after cooling, thus allowing specific recognition by different MAbs. The critical modification of the protein structure was found to take place at 75°C. Two main conclusions can be drawn from these results: (i) heat and enzymatic denaturation of ovalbumin led to similar antigenic modifications—these may be explained by the exposure of hydrophobic residues in both HDOA and PK as evidenced from 8‐anilino‐1‐sulphonic acid fluorescence spectra; (ii) the panel of ovalbumin‐specific MAbs was able to differentiate between the various heat treatments which had been applied to ovalbumin within the range 65–85°C, even after subsequent cooling. The aggregation of ovalbumin molecules during the heating process constitutes the main type of antigenic modification.     

Specific heat of bone

The specific heat of dry bone, as well as decalcified bone, obtained from bovine femur samples are measured as a function of temperature in the range 200 to 390K, using a differential-scanning-calorimetry technique. Special sample pans for volatile materials were used to provide a uniform thermal environment and to eliminate errors due to the evaporation of the moisture contained in the bone samples; the rate of heating was 10 K/min. From measurements of the constant pressure values, and using the Nernst-Lindermann equation, the constant-volume specific heat of both the collage and hydroxyapatite components are evaluated in the given temperature range.     

Differential expression of CD22 (Lyb8) on murine B cells

Previous studies have established the distribution, biochemistryand functional attributes of human CD22, a B cell-restrictedglycoprotein. Recently, molecular cloning of the murine CD22equivalent revealed this molecule to be the same as the previouslydescribed Lyb8 alloantigen. Using the anti-Lyb8 mAb Cy34.1.2,the present report documents the expression patterns of CD22within the murine B cell compartment. The results demonstratethat in the bone marrow, murine CD22 is absent on the surfaceof pro-B cells, pre-B cells and newly emerging lgM⁺ B cells.CD22 is present at a low density on immature IgM^hi B cells andfully expressed on mature recirculating B cells. In the periphery,murine CD22 is expressed at mature levels on all B cell subsetsincluding follicular, marginal zone, B1 and switched B cells.Further studies showed CD22 to be retained on activated murineB cells for extended periods. Finally, in combination with CD23and heat stable antigen, CD22 can be used to delineate the immaturesplenic B cells, and distinguish them from follicular and marginalzone cells. Together, the results demonstrate murine CD22 tobe a useful pan marker for all mature B cell subsets.     

Identification of human T cell epitopes in the Mycobacterium leprae heat shock protein 70-kD antigen.

In a number of pathogens, heat shock proteins (hsp) stimulate humoral and cellular immune responses despite significant sequence identity with host hsp. The 70-kD hsp of Mycobacterium leprae, which shares 47% identity with human hsp70 at the protein level, elicited a T cell response in most Myco. bovis (bacille Calmette-Guérin (BCG)) vaccinees as well as leprosy and tuberculosis patients and their contacts. In order to locate T cell epitopes, DNA fragments encoding portions of the 70-kD hsp were expressed in the vector pGEX-2T and tested for T cell reactivity in an in vitro proliferative assay. Cultures of peripheral blood mononuclear cells (PBMC) from BCG vaccinees indicated that the C-terminal half of the molecule contained multiple T cell epitopes, as the T cells from a majority of Myco. leprae hsp70-reactive individuals responded to C-344. Lower proportions of patients with paucibacillary leprosy (36%) and tuberculosis patients (16%) responded to C-344. The smaller C-142 fragment which includes the terminal 70 residues unique to Myco. leprae and is the target for the human antibody response elicited a cellular response in few patients and no vaccinees. In order to map T cell epitopes, two series of synthetic peptides encompassing the region 278-502 were prepared. Using overlapping 12mer and 20mer peptides, this region of the molecule was found to contain several potential T cell epitopes. The longer peptides gave a clearer indication of reactive sequences including regions of the molecule which were not identified with the 12mer peptides. Fine mapping of reactive peptide pools using the 12mer peptides identified two T cell epitopes. Although both were located in regions of the molecule shared with Myco. tuberculosis, one appeared to be cross-reactive with the equivalent human sequence, and thus has the potential to initiate autoimmune responses.     

Artificial adaptation to cold produced by noradrenalin

The state of muscular heat production 2–3 weeks after intravenous injection of noradrenalin was studied during exposure to cold. A single injection of noradrenalin was found to facilitate maintenance of temperature homeostasis for several weeks with a greatly reduced electrical activity of the muscles and before the noradrenalin was given. The phenomenon probably lies at the basis of adaptation of animals to cold.Laboratory of Temperature Regulation, I. P. Pavlov Institute of Physiology, Academy of Sciences of the USSR, Leningrad. (Presented by Academician V. N. Chernigovskii.) Translated from Byulleten', Éksperimental'noi Biologii i Meditsiny, Vol. 81, No. 3, pp. 286–289, March, 1976.     

Effects of luminal stimuli on polyamine metabolism in the small intestine of the rat: the role of enteric nerves

The aim of this study was to investigate to what extent polyamine metabolism in the small intestine of the rat is controlled by the enteric nervous system. Polyamine metabolism was followed by measuring the activity of ornithine decarboxylase (ODC) and in some instances also the content of polyamines (putrescine, spermidine and spermine). ODC activity in the intestine was increased when intraluminal pressure was increased and 3 h after placing cholera toxin in the intestinal lumen. Cholera toxin also increased the tissue putrescine content. Atropine or hexamethonium given i.v. did not influence the evoked changes of ODC activity. The pressure induced changes were not decreased by placing lidocaine on the serosal surface. On the other hand, the ODC activity of control segments were decreased by hexamethonium or atropine. The presence of glucose in the intestinal perfusate did not augment tissue ODC activity, neither did the heat stable enterotoxin from Escherichia coli (STa). It is concluded that the effect on polyamine metabolism evoked by luminal pressure or cholera toxin seems not to be mediated via nerves, while nerves seem to influence ODC activity during control conditions. The experiments with enterotoxins suggest that cAMP is the intracellular second messenger controlling intestinal ODC activity.     

Increase of fetal arterial blood temperature by reduction of umbilical blood flow in chronically instrumented fetal sheep

The effect of reduced umbilical blood flow rate on fetal core temperature was investigated in five chronically instrumented fetal sheep (gestational age 124 days). On average, fetal-maternal temperature difference increased 0.13±0.02 °C when blood flow rate was decreased to about 1/3 of normal (248±69 ml min^–1) for 30 min. The small temperature rise is the consequence of predominant heat dissipation through the placenta, and of diminished oxygen consumption.     

Emigration of selected subsets of {gamma}{delta}+ T cells from the adult murine thymus

Cells bearing the form of the TCR make up only 1–3% ofT cells in the adult murine thymus and peripheral lymphold organs.Evidence from studies of nude mice suggests that the developmentof at least some T cells is thymus dependent; however, untilnow it has not been directly demonstrated that cells are exportedfrom the thymus. In this paper we have used the technique oflabelling thymocytes in vivo with FITC, followed by flow cytometrlcanalysis to trace cells emigrating from the thymus to the spleen.Using this approach we have been able to demonstrate for thefirst time that T cells are exported from the adult murinethymus to the spleen. We also demonstrate that the cells emigratingto the spleen are a selected subset of thymocytes being heatstable antigen positive, Thy-1⁺, and expressing low levels ofCD44 (Pgp-1). In addition, investigation of TCR V; gene usageamong adult ⁺ thymocytes, recent emigrants, and spleen cells,indicated a selective emigration of cells expressing certainVgenes.     

脑室注射促甲状腺素释放激素对电针镇痛及脑内亮氨酸脑啡肽含量的影响

实验用大鼠76只,用辐射热-甩尾法测痛,以电针后痛阈变化的百分率评价镇痛效应;用放射免疫分析法测定脑内L-Enk含量。发现脑室注入三肽-促甲状腺素释放激素(TRH)后,能显著降低电针镇痛效果;提高丘脑内L-Enk含量,但痛阈与脑内L-Enk含量的变化无相关关系。本文证明,TRH在电针镇痛过程中是对抗作用。已知针刺镇痛与脑内多种神经质和肽类有关,在不利于针刺镇痛的因素中,TRH是新添的“一员”。