scholarly journals HEPATIC BIOTRANSFORMATION PROFILES OF SULPHAMONOMETHOXINE IN FOOD-PRODUCING ANIMALS AND RATS IN VITRO

2000 ◽  
Vol 48 (3) ◽  
pp. 293-300 ◽  
Author(s):  
N. Furusawa

Hydroxylation and acetylation of sulphamonomethoxine (SMM) and deacetylation of N4-acetyl SMM (N4-AcSMM) were estimated in liver post-mitochondrial supernatants (S-9) from laying hens, female cattle, swine and rats. The formation of hydroxylated SMM, 2,6-dihydroxy SMM (2,6-diOH-SMM), was found only with hen S-9s. N4-acetylation rate of SMM was the highest in pig S-9s, followed by rat, then hen or cow S-9s. All S-9s from the four species deacetylated N4-AcSMM. In hen S-9s, the rate of 2,6-dihydroxylation was higher during incubation at 41 °C than at 37 °C.

2001 ◽  
Vol 49 (3) ◽  
pp. 349-353
Author(s):  
N. Furusawa ◽  
Y. Morita

The hepatic biotransformation of aldrin (AD) and dieldrin (DD) was studied in liver post-mitochondrial supernatants (S-9s) from laying hens, female cattle and swine. S-9s were incubated with 0.03 nmol o f AD or DD for 1 h. After 1 h, AD in the samples was almost epoxidated to DD. This formation was found with all the animal S-9s, and the highest rates occurred in pig S-9 (P < 0.01), followed by cow and hen S-9s. No reduction of DD was found with any of the S-9s.


1972 ◽  
Vol 50 (7) ◽  
pp. 721-724 ◽  
Author(s):  
Norman R. Bade ◽  
Stuart M. MacLeod ◽  
Kenneth W. Renton

Preliminary experiments were undertaken to examine the effect of three hydrazine derivatives, viz. Ro 4-4602, MK 486, and procarbazine hydrochloride, on hepatic microsomal drug metabolism in rats. All three compounds when given as pretreatment significantly prolonged pentobarbital sleeping time. In vitro, the hepatic microsomal N-demethylation of aminopyrine was inhibited. It is concluded that all three drugs are possible sources of clinically significant drug interaction when administered in combination with other agents which undergo hepatic biotransformation.


2020 ◽  
Author(s):  
Sicheng Xing ◽  
Chunbo Huang ◽  
Ruiting Wu ◽  
Yiwen Yang ◽  
Jingyuan Chen ◽  
...  

Abstract Background: The microbiota in the cecum of laying hens was critical for host digestion metabolism and odor gas production. Recent studies have suggested that host miRNAs could regulate gene expression in the gut microbiota. The expression profiles of host-derived miRNAs in the cecal content of two laying hen breeds, Hy-line Gray and Lohmann Pink, which have dissimilar H2S production were characterized, and their possible effects on H2S production by regulating the expression of related genes in the microbiota were demonstrated. Results: The differential expression of microbial serine O-acetyltransferase, methionine synthase, aspartate aminotransferase, methionine-gamma-lyase and adenylylsulfate kinase between the two breeds resulted in lower H2S production in the Hy-line hens. The results also demonstrated miRNA exosomes in the cecal content of laying hens and the potential miRNA-target relationships between 9 differentially expressed miRNAs and 9 differentially expressed microbial genes related to H2S production were investigated, among which gga-miR-222a targeted two methionine synthase genes, Odosp_3416 and BF9343_2953. An in vitro fermentation experiment showed that gga-miR-222a upregulated the expression of these genes, which increased methionine concentrations but decreased H2S production and soluble sulfide concentrations, indicating the potential of host-derived gga-miR-222a to reduce H2S emission in laying hens. Conclusion: These findings identify both a physiologic role by which miRNA shapes the cecal microbiota of laying hens and a strategy to use host miRNAs to manipulate the microbiome and actively expressed key microbial genes to reduce H2S emission and breed environmentally friendly laying hens.


Toxicon X ◽  
2020 ◽  
Vol 6 ◽  
pp. 100031
Author(s):  
Morten Sandvik ◽  
Christopher O. Miles ◽  
Alistair L. Wilkins ◽  
Christiane Fæste

1982 ◽  
Vol 206 (3) ◽  
pp. 647-654 ◽  
Author(s):  
H Griffin ◽  
G Grant ◽  
M Perry

Very-low-density (VLD) lipoproteins and portomicrons were isolated from the plasma of immature and laying hens and their size, lipid composition and susceptibility to hydrolysis by lipoprotein lipase were compared. In agreement with other studies, VLD lipoproteins from laying hens were found to be smaller and have a different lipid composition than VLD lipoproteins from immature hens. Portomicrons from immature and laying hens had mean diameters of about 150 nm and similar lipid compositions. Hydrolysis of VLD lipoproteins from immature hens, and portomicrons from immature and laying hens, proceeded rapidly until at least 40% of the substrate had been used. In contrast only 1-15% of laying-hen VLD-lipoprotein triacylglycerol was readily hydrolysis occurred slowly. The limited susceptibility of laying-hen VLD lipoproteins appeared to be due to their low content of lipoprotein lipase activator apoprotein, which occurred despite an abundance of activator in the high-density lipoproteins of laying-hen plasma. The results provide further evidence that the liver of the laying hen synthesizes specialized lipoproteins. Their limited susceptibility to hydrolysis by lipoprotein lipase is probably a major factor in ensuring transport of lipid to yolk rather than to other tissues. The form of transport of dietary lipid, however, is similar in immature and laying hens.


1990 ◽  
Vol 127 (3) ◽  
pp. 487-496 ◽  
Author(s):  
S. C. Wilson ◽  
R. A. Chairil ◽  
F. J. Cunningham ◽  
R. T. Gladwell

ABSTRACT The contents of LHRH-I and -II in the anterior hypothalamus and posterior hypothalamus (including the mediobasal hypothalamus and median eminence) were measured at 90, 180 and 360 min after the i.m. injection of laying hens with progesterone. Whilst no changes were observed in the content of LHRH-I in the anterior hypothalamus, LHRH-I in the posterior hypothalamus tended to fall at 90 and 180 min after injection of progesterone in hens maintained on 16 h light:8 h darkness (16L:8D) and 8L:16D respectively. Pretreatment of laying hens with tamoxifen significantly increased the hypothalamic contents of LHRH-I and -II, raised the basal plasma concentration of LH and modified the LH response to progesterone injection. In hens in which tamoxifen prevented an increase in the plasma concentration of LH after progesterone injection, the content of LHRH-I in the posterior hypothalamus remained unchanged. In contrast, in hens in which progesterone stimulated a steep increase in LH within 90 min, there was a pronounced and significant fall in LHRH-I content of the posterior hypothalamus. No change in the hypothalamic content of LHRH-II was observed during the progesterone-induced surge of LH until plasma concentrations had attained maximal values or started to decline. Then, in hens maintained on 16L:8D, a significant fall in the content of LHRH-II in the anterior hypothalamus was found at both 180 and 360 min after injection with progesterone. Tests in vitro and in vivo of the responsiveness of the pituitary gland to synthetic LHRH-I and -II revealed no change at 90 min after injection of laying hens with progesterone, when plasma concentrations of LH were increasing, but a pronounced reduction when plasma LH concentrations were maximal or falling. These results suggest that LHRH-I mediates in the progesterone-induced increase in the plasma concentration of LH. Although the subsequent decline in plasma LH was associated with a reduced responsiveness of the pituitary gland to LHRH, a significant correlation between the contents of LHRH-I and -II in the anterior hypothalamus and a fall in the hypothalamic content of LHRH-II when plasma LH was maximal or declining allows the possibility of an involvement of this peptide in the neuroendocrine events preceding ovulation. Journal of Endocrinology (1990) 127, 487–496


2017 ◽  
Vol 65 (35) ◽  
pp. 7647-7652 ◽  
Author(s):  
Xueke Liu ◽  
Peng Wang ◽  
Chang Liu ◽  
Yiran Liang ◽  
Zhiqiang Zhou ◽  
...  

1956 ◽  
Vol 54 (3) ◽  
pp. 419-432 ◽  
Author(s):  
H. Williams Smith

1. A good immunity was produced in chickens against oral infection with Salm. gallinarum by the use of either of two live attenuated vaccines, one smooth, 9S and one rough, 9R. Dead vaccines had little or no effect.2. The immunity possessed by chickens vaccinated with 9R at 7 weeks of age commenced to wane 12 weeks later. Chickens similarly vaccinated with 9S were completely immune 4, 12 and 34 weeks later. When tested during the active laying period (at 20 weeks after vaccination) their immunity, although substantial, was not complete.3. Vaccine 9R did not produce demonstrable agglutinins against smooth Salm. gallinarum in chickens. It was non-lethal to 1-day-old chicks and was never found to revert to the smooth virulent form in vitro or in vivo. By contrast, vaccine 9S produced agglutinins and was lethal for 1-day-old chicks, its virulence not being increased by passage. No deaths were ever observed when this vaccine was used in either chickens of 5–12 weeks old or laying hens.4. Although both vaccines produced a good immunity when employed in laying hens, vaccination with 9S was accompanied by a marked reduction in egg production; this was not the case with 9R.5. An immunity of the interference type was also evoked by both live vaccines. This immunity was still produced to some extent in chickens injected with 9S, 2 days after they were infected with Salm. gallinarum by mouth.6. The interference effect could not be produced by the use of either dead Salm. gallinarum vaccines or certain non-specific substances. The intravenous injection of indian ink had a marked adverse effect on the course of the disease. Injecting chickens with a virulent strain of Bacterium coli at the same time as they were infected with Salm. gallinarum resulted in the latter infection running a milder course than would normally have been expected.


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