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Biomedical subjects

X Zhao

Publications and source records attributed to X Zhao.

At least 667 records · Page 37Linked to original sources

Effect on production traits of bovine somatotropin for up to three consecutive lactations.

Thirteen (control) cows were injected daily with saline and 22 with bST (12 at 10.3 mg/d and 10 at 20.6 mg/d) through wk 5 to 42 of lactation. Nine of the treated cows had received bST in the previous lactation, and 7 cows received bST in the previous two lactations. All control cows and 6 treated cows had not previously received bST. Treatment with bST caused substantial increases in milk production, feed intake, and efficiency of feed conversion in the current lactation, which is consistent with previous trials. Increases in feed intake were established fully within 9 wk of starting bST administration, somewhat earlier than usually reported. Treatment with bST in one or two previous lactations caused a statistically significant 14% reduction in production and 8% reduction in efficiency of feed conversion during the first 9 wk of bST treatment in the current lactation; reductions observed later in lactation were not statistically significant. Differences for other traits were not statistically significant. In combination with earlier trials, these results suggest that, although bST has beneficial effects on production and efficiency traits, these benefits may be considerably lower in the second and subsequent lactations of bST use. However, carry-over effects on cows not receiving bST in the current lactation were not explored in this trial.

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Lactation, health, and reproduction of dairy cows receiving daily injectable or sustained-release somatotropin.

Seventy-four Holstein cows (26 primiparous) were utilized to compare the efficacy and safety of sustained-release versus daily injectable formulations of recombinant bST. Twenty-four control cows were injected biweekly with oil microsphere; 25 cows were injected biweekly with 350 mg of bST microsphere; and 25 cows were injected daily with 10.3 mg of bST. Injections were initiated between wk 4 and 5 of lactation and continued for 280 d. Administration of bST caused a moderate increase in milk and FCM production and improved the efficiency of feed and energy conversions. Most health-related and reproduction-related variables did not differ among treatment groups. However, incidence of teat and udder disorders and feet and leg problems tended to be higher during the 40-wk injection period for the bST-treated cows than for the control cows. Incidence of GnRH therapy and number of days to first service were higher for daily bST-treated cows than for controls. No differences existed between sustained-release and daily bST-treated cows for any parameters monitored.

Animals↗

[Hybridization experiments using Anopheles minimus from Guangxi and Yunnan].

Hybridization experiments were conducted by forced mating between Anopheles minimus from Guangxi (G) and Yunnan (Y). F1 hybrid females were all fertile with normally developed ovaries. (Y female x G male) F1 males were all sterile, with abnormally enlarged testes. (G female x Y male) F1 males, though fertile, showed somewhat atrophic testes, and when they were back crossed with parental females, the latter produced eggs with very low hatching rate. Ovarian nurse cell polytene chromosomes from F1 hybrid females showed partial asynapsis in X chromosome as well as in autosonles, asynapsis at 38 zone in 3L being the most constant. It was obvious that there was definite, though partial, reproductive isolation between An minimus from Guangxi and that from Yunnan. Whether they are sibling species remains to be further investigated (Figs. 1-8).

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[Quality of dihuang (Rehmannia spp.)].

In this paper, the contents of catalpol, water-extract and alcohol-extract materials, ash, total reducing sugar and inorganic elements in Dihuang from different habitats have been measured. The result shows that Huai Dihuang, the genuine drug, excels all those from other habitats in quality. The quality of commercial dry Dihuang may be related closely to the production area, storage time, etc.

Calcium↗

[Isolation and identification of a strain of Pseudomonas SP. producing insoluble glucan hydrolase].

A strain, CIB871, isolated from the natural world can hydrolyze insoluble glucan(IG) produced by S. mutans. This organism has been identified to be a strain of Pseudomonas SP. It grows well at 30 degrees C. The optimum medium for producing insoluble glucan hydrolase (IGase) is composed of 0.3% peptone, 0.03% IG and M1 salt solution (NH4)2 SO4 1mg/ml, MgSO4 50 micrograms/ml, FeCl2 50 micrograms/ml, K2HPO4 0.5mg/ml). The IGase production reached maximum when cultured for 65-70 hours.

Glucans↗

Flavin-containing monooxygenase: a major detoxifying enzyme for the pyrrolizidine alkaloid senecionine in guinea pig tissues.

Evidence based on optimal pH, thermal stability, and enzyme inhibition data suggests that the NADPH-dependent microsomal N-oxidation of the pyrrolizidine alkaloid senecionine is carried out largely by flavin-containing monooxygenase in guinea pig liver, lung, and kidney. In contrast, the hepatic microsomal conversion of senecionine to the pyrrole metabolite (+/-)-6,7-dihydro-7-hydroxy-1-hydroxymethyl-5H-pyrrolizine (DHP) is catalyzed largely by cytochrome P450. However, the rate of senecionine N-oxide formation (detoxication) far exceeded the rate of DHP formation (activation) in guinea pig liver microsomes over a range of pHs (pH 6.8 to 9.8). In guinea pig lung and kidney microsomes, N-oxide was the major metabolite formed from senecionine with little or no production of DHP. The high rate of detoxication coupled with the low level of activation of senecionine in liver, lung, and kidney may help explain the apparent resistance of the guinea pig to intoxication by senecionine and other pyrrolizidine alkaloids.

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Comparison of rainbow trout and mammalian cytochrome P450 enzymes: evidence for structural similarity between trout P450 LMC5 and human P450IIIA4.

Studies were undertaken to determine the immunochemical relationship between constitutive trout cytochrome P450s and mammalian cytochrome P450IIIA enzymes. Polyclonal antibodies (IgG) generated against trout P450 LMC5 reacted strongly with P450IIIA1 in dexamethasone-induced rat liver microsomes and with P450IIIA4 in human liver microsomes in immunoblots. In contrast, rabbit anti-P450 LMC1 IgG did not recognize these proteins in rat and human liver microsomes. Reciprocal immunoblots using anti-rat P450IIIA1 showed that this antibody does not recognize trout P450 LMC1 or LMC5. However, anti-human P450IIIA4 IgG was found to cross react strongly with P450 LMC1 and LMC5. Progesterone 6 beta-hydroxylase activity of trout liver microsomes, a reaction catalyzed by P450 LMC5, was markedly inhibited by anti-P450IIIA4 and by gestodene, a mechanism-based inactivator of P450IIIA4. These results provide evidence for a close structural similarity between trout P450 LMC5 and human P450IIIA4.

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IGF-I receptors in embryonic skeletal muscle of three strains of chickens selected for differences in growth capacity.

IGF-I receptors in embryonic skeletal muscle from three strains of chickens have been characterized. Specific receptors for IGF-I were present in breast and thigh skeletal muscle of 13 d chicken embryos. Dissociation rate constants (Kd) for breast muscle of a slow growing layer strain (Leghorn), an intermediate growth strain (Synthetic Whiterock), and a fast growing broiler strain (Cornish) were 3.24, 3.04, and 2.68 nM, respectively. Kd for the thigh muscle of the slow, intermediate and fast growing strains were 3.30, 2.90 and 3.29 nM, respectively. Kd values were not significantly different between strains or between tissues (p greater than .05). Receptor concentration (Bmax) in breast muscle of slow, intermediate and fast growing strains were 1.22, 1.08 and 0.92 pM/mg protein, respectively. Receptor concentration in thigh muscle of the slow, intermediate and fast growing strains were 0.95, 0.76, and 0.79 pM/mg protein, respectively. Bmax values were significantly different (p less than .05) between breast muscle (1.08 +/- .05 pM/mg protein) and thigh muscle (.84 +/- .05 pM/mg protein). IGF-I receptor number for breast muscle although not statistically significant (p greater than .05), indicated a trend towards differences between the slow growing Leghorn strain and the faster growing Cornish strain. The results suggest that strains of birds with different growth capacity may have different densities of IGF-I receptors in breast skeletal muscle plasma membranes.

Animals↗

Disproportionate alpha- and beta-mRNA sodium pump subunit content in canine vascular smooth muscle.

Total RNA isolated from canine saphenous vein smooth muscle cells was examined for Na+ pump alpha- and beta-mRNA content by three increasingly sensitive methods: Northern analysis, RNase protection assay, and polymerase chain reaction. Northern analysis clearly showed the presence of beta-mRNA. An alpha 1 signal was not demonstrable using either Northern analysis with a 1.5-kb cDNA probe or RNase protection. However, an "alpha 1-like" transcript was detected using polymerase chain reaction with two sets of primers constructed to selected areas of the rat alpha 1-cDNA. These data suggest that beta-mRNA in canine blood vessels is in large excess of the alpha 1-mRNA. This discrepancy may be reflected in the relatively low number of Na+ pump sites in this tissue.

Animals↗

Effect of bovine skim milk and whey on monocyte function.

Previous studies have documented the ability of bovine milk to inhibit lymphocyte proliferation in response to mitogens. It is not known whether inhibition of lymphocyte proliferation is mediated through the action of monocytes. To address this question, we examined the ability of bovine skim milk and whey to affect monocyte function with emphasis on expression of major histocompatibility class II antigens and production of interleukin-1 by monocytes. Data showed that expression of major histocompatibility complex class II molecules and production of interleukin-1 by monocytes were not altered when monocytes were cultured in the presence of bovine skim milk or whey. Thus, it is unlikely that the suppressive effect of milk on lymphocyte proliferation could be mediated through alterations in the expression of major histocompatibility class II molecules or in production of interleukin-1 by monocytes. The role of other monocyte antigens or secretory products, however, should also be evaluated.

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