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Biomedical subjects

H Yang

Publications and source records attributed to H Yang.

At least 991 records · Page 55Linked to original sources
PubMed1989

[Measurement for instantaneous acceleration of ventricular pressure and its significant].

The indices of the first and second derivatives of the left ventricular pressure were compared in terms of their inotropic sensitivity and preload, afterload and heart rate dependence in 14 rabbits. In comparison with (dp/dt)max, (d2p/dt2)max is more sensitive to inotropic stimulation. Both indices are increased with increasing preload, afterload and heart rate (HR), but the difference in their dependences on load and HR is not statistically significant. The results suggest that (d2p/dt2)max is a better index of ventricular performance than (dp/dt)max.

Acceleration↗
PubMed1988

Effects of oestradiol benzoate injections, exposure to the boar and age on the attainment of puberty in the gilt.

Thirty large white cross Landrace prepubertal gilts from five litters were allocated at random within litters to one of six treatment. All the gilts were given three daily intramuscular injections of 6 micrograms/kg liveweight of oestradiol benzoate but the first injection was given at either 100 days, 120 days, 140 days, 160 days, 180 days or 200 days old. From the time the first oestrogen injection was given, until the end of the experiment, the gilts were allowed daily contact with a boar for 20 minutes. The gilts were mated with a mature boar at the appearance of the second oestrus and they were slaughtered 20 days later. The numbers of gilts ovulating in the treatment groups were determined from plasma progesterone concentrations measured twice weekly throughout the experiment. The numbers of gilts ovulating within 10 days of the oestradiol benzoate injections were 3 of 5, 1 of 5, 0, 0, 3 of 5 and 1 of 5, respectively, in the groups first treated at 100 days, 120 days, 140 days, 160 days, 180 days and 200 days old. For those gilts which were successfully mated, no significant differences were observed between the treatment groups in the number of viable embryos per gilt.

Age Factors↗
PubMed1988

The epidemiology of childhood burns in Jiamusi, China.

The causes and severities of burning injury were analysed in 1006 children admitted to our department over a 11-year period. A substantial number of patients were less than 5 years old. Proportionally more boys and less girls were injured. More of the accidents occurred in summer and winter and less during the spring and autumn; more occurred in the rural and mountain areas than in the cities. In the younger children 88 per cent of the injuries occurred at home while eating and drinking, only a few burns happening in kindergarten and school. This report suggests which methods of prevention should be stressed.

Burns↗
PubMed1988

Medullary sites of action of the TRH analogue, RX 77368, for stimulation of gastric acid secretion in the rat.

Brain and spinal sites of action of the stable thyrotropin-releasing hormone (TRH) analogue, RX 77368 [pGlu-His-(3,3'-dimethyl)-Pro-NH2], for stimulation of gastric acid secretion have been investigated in urethane-anesthetized rats with gastric fistula. RX 77368 microinjected at a 7.7-pmol dose into the dorsal vagal complex or nucleus ambiguus stimulated gastric acid secretion to 62.2 +/- 15.9 and 45.3 +/- 14.3 mumol/h, respectively, whereas in the vehicle-treated group acid secretion was 0.5 +/- 1.0 mumol/h. A 10-fold higher dose of RX 77368 was inefficient when microinjected into the medial septum, central amygdala, or lateral hypothalamus. The gastric secretory response to microinjection of RX 77368 into the nucleus ambiguus was dose related (0.7-77 pmol), long-lasting (greater than 90 min), and blocked by vagotomy. TRH (144 pmol) injected into the nucleus ambiguus also stimulated gastric acid secretion but was less potent than the stable TRH analogue, whereas the unrelated peptide, oxytocin, was inactive. Intrathecal injection of RX 77368 at doses up to 2500 pmol did not modify gastric acid secretion. These results demonstrate that the dorsal vagal complex and nucleus ambiguus are TRH sites of action for stimulation of gastric acid secretion through vagal dependent pathways. These findings, added to the high concentrations of TRH-like immunoreactivity and receptors present in these nuclei, suggest a possible role of medullary TRH in the vagal regulation of gastric acid secretion.

Animals↗
PubMed1988

Antiviral effect of lymphokine-activated killer cells: characterization of effector cells mediating prophylaxis.

Lymphokine-activated killer (LAK) cells generated by cultivation of C57BL/6 mouse spleen cells in the presence of recombinant interleukin-2 were transferred into natural killer (NK) cell-deficient suckling mouse recipients. These mice were then challenged with either murine cytomegalovirus (MCMV) or lymphocytic choriomeningitis (LCMV) and sacrificed 3 days later. No interleukin 2 infusions were given. Mice receiving as few as 5 x 10(5) LAK cells had several 100-fold decreases in spleen MCMV titers as compared with untreated mice. This treatment had no effect on spleen LCMV titers. The LAK cell cultures contained 10 to 17% NK 1.1+, 50 to 55% Lyt-2+, and 33 to 50% immunoglobulin D+ cells. Double fluorescence labeling and in vitro cytotoxicity assays with fluorescence-activated cell sorting revealed at least two mutually exclusive killer cell populations. NK 1.1+ LAK cells resembled freshly isolated activated NK cells with regard to target cell range (YAC-1 cell killing greater than L-929, P815, and EL-4 cell killing), large granular lymphocyte (LGL) morphology, and decreased ability to lyse interferon (IFN)-treated target cells. Lyt-2+ LAK cells lysed the targets mentioned above but at lower levels and without the differences in susceptibility mentioned above. These Lyt-2+ LAK cells also had a decreased ability to lyse IFN-treated targets, in contrast to classic cytotoxic T lymphocytes, which lyse IFN-treated targets far more efficiently than untreated targets. Purified populations of LAK cells obtained by fluorescence-activated cell sorting were used in the antiviral protection model. The results showed that protection against MCMV could be mediated by NK 1.1+, NK 1.1-, Lyt-2+, Lyt-2-, and IgD- populations but not by IgD+ cells. The five protective populations all had in common the LGL phenotype and cytotoxic activity in vitro. The IgD+ population did not contain LGLs, lyse target cells in vitro, or mediate an antiviral effect in vivo. These results suggest that LAK cells may be therapeutically useful against certain virus infections (MCMV) but not others (LCMV) and that despite their heterogeneity in antigenic phenotype and cytotoxic activity, their pattern of antiviral activity in vivo resembles that of NK cells, which protect against MCMV but not LCMV.

Animals↗
PubMed1987

Purification and properties of Escherichia coli 4'-phosphopantothenoylcysteine decarboxylase: presence of covalently bound pyruvate.

4'-Phosphopantothenoylcysteine decarboxylase was purified 900-fold from Escherichia coli B with an overall yield of 6%. The enzyme migrates as a single band with a molecular weight of 35,000 +/- 3000 in 10% polyacrylamide gel electrophoresis under denaturing conditions. The native enzyme has an apparent molecular weight of 146,000 +/- 9000 as determined by a gel exclusion column. At pH 7.6 and 25 degrees C, Km = 0.9 mM and Vmax = 600 nmol/(min X mg of protein). The pH optimum for Vmax is between 7.5 and 7.7. Hydroxylamine, phenylhydrazine, potassium cyanide, and sodium borohydride as well as pyridoxal phosphate and pyridoxal inactivated the enzyme. The enzyme contains covalently bound pyruvate as suggested by the isolation of [3H]lactate and pyruvate from [3H]NaBH4-reduced enzyme and native enzyme, respectively. One mole of [3H]lactate was isolated per 39,000 g of [3H]NaBH4-reduced and completely inactivated enzyme, and 1 mol of pyruvate was isolated per 31,000 +/- 4000 g of native enzyme. Mild base treatment released lactate and pyruvate from the reduced and the native enzymes, respectively, suggesting the pyruvate is attached to the enzyme by an ester bond. These findings are in accord with similar results obtained with the horse liver enzyme (R. Scandurra, personal communication). The presence of covalently bound pyruvate in the bacterial and mammalian enzymes suggests that pyruvate plays a major role in the mechanism of action.

Binding Sites↗
PubMed1987

Enzymatic transformation of PGH2 to PGF2 alpha catalyzed by glutathione S-transferases.

Glutathione S-transferases (GSTs) purified from both rat liver cytosol and microsomes catalyzed the direct reduction of PGH2 to PGF2 alpha. As much as 40% of the substrate was transformed into a prostanoid whose Rf value corresponded to that of PGF2 alpha. The identification of the reaction product as PGF2 alpha was confirmed by TLC and reverse-phase HPLC as well as by mass spectral analysis. In the absence of GSTs, PGH2 was found to be primarily converted to PGE2 and PGD2. Also, PGF2 alpha formation was completely abolished by decylglutathione, a potent inhibitor of both peroxidase and transferase activity associated with GSTs. These results indicate that the direct reduction of endoperoxide moiety of PGH2 to form PGF2 alpha is an enzymatic process. Interestingly, selenium-dependent glutathione peroxidase (Se-GSH-Px) showed very little PGF2 alpha formation from PGH2. However, this enzyme was very active in the reduction of PGG2 to PGH2. In contrast, GSTs were very poor in the conversion of PGG2 to PGH2. Therefore, it is possible that the relative tissue distribution of Se-GSH-Px and GSTs might play an important role in the tissue specific synthesis of PGF2 alpha.

Animals↗
PubMed1987

Effect of a carbohydrate-restricted, calorie-reduced diet on the growth of young rats and on serum growth hormone, somatomedins, total thyroxine and triiodothyronine, free T4 index, and total corticosterone.

We have studied the effect of a carbohydrate-restricted, calorie-reduced diet on the growth of young rats and on serum levels of GH, somatomedins [insulin-like growth factors (IGFs) I and II], total T4 and T3, free T4 index, and total corticosterone. Experimental animals consumed the same quantities of protein and fat as controls, but only 50.3% as much carbohydrate and 76% as many calories. While the experimental group grew at 69.4% of the control rate, their mean (+/- SEM) GH level (175.7 +/- 36.9 ng/mL) was not significantly different from that in the control group (180 +/- 30 ng/mL). In contrast, serum total IGF and IGF-I, while not correlated with serum GH levels, were significantly correlated in all animals with body weight (r = .87 and r = .82, respectively, P less than .01) and tail length (r = .61 and r = .62, respectively, P less than .01). The somatomedin levels of the carbohydrate-restricted rats were significantly lower than those of their age-matched, but not weight-matched, controls by the eighth day of study. Serum T4, T3, and free T4 index were not significantly different in these two groups, while total corticosterone in the experimental group (245 +/- 73 ng/mL) was slightly lower than in controls (292 +/- 80 ng/mL, P less than .05). These data indicate that by restricting carbohydrate intake we have compromised the anabolic use of dietary protein by growing rats, resulting in a retardation of growth and a reduction in serum total IGF and IGF-I levels.

Animals↗
PubMed1987

Natural killer cells are not required for interferon-mediated prophylaxis against vaccinia or murine cytomegalovirus infections.

Natural killer (NK) cell-depleted or control mice were treated prophylactically with polyinosinic: polycytidylic acid (polyI: polyC) or purified beta interferon (IFN) and then infected with either vaccinia virus or murine cytomegalovirus. NK cell depletion alone enhanced virus titres in the spleen and peritoneal cavity. However, poly I: polyC and IFN inhibited virus replication equally well in control and NK cell-depleted mice. This suggests that prophylactic IFN treatment mediates antiviral effects independently of NK cells.

Animals↗