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Specific nutrients for posthatch poultry and postweaning pigs /Yi, Ganfeng, January 2003 (has links)
Thesis (Ph. D.)--University of Missouri-Columbia, 2003. / Typescript. Vita. Includes bibliographical references (leaves 169-184). Also available on the Internet.
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The role of ion channels in gastric mucosal healingWu, Ka-kei., 胡嘉麒. January 2005 (has links)
published_or_final_version / abstract / Pharmacology / Master / Master of Philosophy
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Neural crest cell development in the nervous system of normal gut and in Hirschsprung's diseaseFu, Ming, 付明 January 2003 (has links)
published_or_final_version / abstract / toc / Surgery / Doctoral / Doctor of Philosophy
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The physiological role of transforming growth factor-beta in gastrointestinal development in the pigMei, Jie, 梅節 January 2004 (has links)
published_or_final_version / abstract / toc / Zoology / Doctoral / Doctor of Philosophy
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Upper gastrointestinal mucosal blood flow in health and diseaseOng, Leslee Y. January 1999 (has links)
published_or_final_version / Medicine / Master / Master of Philosophy
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The Epidemiology of Clostridium perfringens type A on Swine Farms in Ontario and the Perceived Role in Neonatal Piglet EnteritisChan, Gloria 11 May 2012 (has links)
To study the distribution of Clostridium perfringens and toxin genes, 48 swine farms were visited and 354 fecal samples were collected. The isolates recovered from lactating sows, gestating sows, grower-finishers, and manure pits were less likely to possess consensus gene cpb2 compared to those from suckling pigs (P<0.05). The relative importance of different pathogens associated with neonatal piglet diarrhea was identified. A total of 237 neonatal diarrhea cases were submitted to the Animal Health Laboratory, University of Guelph between 2001 and 2010. The combined frequencies for cases involving enterotoxigenic Escherichia coli, Clostridium perfringens type A, rotavirus, and Clostridium difficile accounted for 56% of the total cases. A survey was administered to 22 practitioners and 17 pathologists for the diagnosis of C. perfringens type A. The majority (95%) of practitioners were moderately to very confident of their diagnosis, but almost half (41%) of the pathologists were not confident of their diagnosis. / Ontario Ministry of Agriculture Food and Rural Affairs
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The effect of water sprinkling market pigs transported during summer on pig behaviour, gastrointestinal tract temperature and trailer micro-climate.Fox, Jessica 10 January 2013 (has links)
There has been little research into the use of water cooling methods for pigs during transport to slaughter under conditions of high ambient temperature. The aim of this study was to examine the effects of water sprinkling pigs before departure from the farm and before unloading at the plant on behaviour during transport, unloading and lairage using live and remote observations, and on pig gastrointestinal tract temperature (GTT) and trailer micro-climate measured by data loggers. Above 23oC, the use of water sprinkling tended to decrease GTT upon arrival and significantly decreased drinking bouts during lairage. There were no detrimental effects of the water sprinkling on unloading behaviours (e.g. slips and falls) or on trailer micro-climate conditions in terms of temperature, humidity or ammonia. Water sprinkling to wet the skin of pigs can therefore be used to cool pigs during transport and lairage under high ambient temperatures.
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The effect of alcohol, isoniazid, rifampicin, paracetamol and hexane on hepatic gluconeogenesis and bromosulphthalein clearance.Khedun, Shaun Mahabeer. January 1988 (has links)
The first workers to use the isolated perfused rat liver for the study of gluconeogenesis
were Corey and Britton (1941). Subsequently, other investigators found the modified
method of Miller et al (1951) to be more suitable. This technique, with modifications introduced
by Mortimore (1961) and Hems et al (1966) was used in the present study.
The isolated liver is perfused through the portal vein with saline, supplemented by bovine
serum albumin and washed human erythrocytes, under a pressure of about 20cm of water,
maintained by a reservoir of adjustable height. The perfusate which passes through the
liver enters the inferior vena cava and passes, via a cannula, to a collecting vessel from
which it is pumped to the top of a multiple bulb oxygenator and then returned to the liver
for re-perfusion. This technique has proved to be a satisfactory means of assessing
changes in the metabolic status of hepatic cells in response to starvation and exposure to
halothane.
The study described here was performed to determine whether the isolated liver perfusion
technique can be used to measure the effects on liver perfusion of therapeutic and supratherapeutic
doses of various drugs, some of which have been reported to affect liver metabolism
adversely in the intact animal.
Liver function was assessed by studying gluconeogenesis and bromosulphthalein
clearance. Alcohol and hexane were administered in toxic doses, rifampicin and isoniazid
in high doses and paracetamol in therapeutic doses.
Inbred male Wistar rats were used for these studies. Hexane was injected subcutaneously,
while the other drugs were given per os on 7 consecutive days each week for
a period of 90 days; with the exception of the control group in the hexane study, all the
control groups were untreated.
Pyruvate, a precursor for gluconeogenesis (synthesis of glucose from non-carbohydrate
sources) is an excellent substrate for the formation of oxaloacetate, which is probably an
obligatory intermediate in the pathway to glucose synthesis. It has been used over a number
of years by different investigators who have .studied gluconeogenesis using the isolated
liver perfusion technique. It was used for the same purpose in the present study.
Methylene blue, a redox dye, capable of oxidising NADH to NAD+, was used to determine
whether an altered NADH : NAD+ ratio would have any effect on the output of glucose in
the ethanol, paracetamol and hexane studies. Fructose, a non-NAD+ dependent precursor
of glucose. was also used for this purpose in the ethanol study.
All the drugs studied were found to inhibit gluconeogenesis. This was shown by a
decrease in glucose levels and an increase in lactate : pyruvate ratios in the perfusion
medium of experimental livers. The decreased glucose production by the experimental
livers, which occurred pari passu with an increased pyruvate utilization, indicates that in
these animals pyruvate was used for the production of other compounds such as lactate.
In contrast. glucose production and pyruvate utilization were increased in the control
group indicating that pyruvate was used mainly for the production of glucose.
In the ethanol group, impaired gluconeogenesis was probably due to a change in the
NADH : NAD+ ratio; when methylene blue was introduced into the perfusion medium of
this group the output of glucose was high.
Impaired gluconeogenesis in the paracetamol and hexane-treated groups was probably
related to the non-availability of oxaloacetate or impairment of the activity of key enzymes
involved in gluconeogenesis; when methylene blue was added to the perfusion medium of
these animals the glucose output remained low.
Except for the rifampicin study. bromosulphthalein clearance was impaired in all the experimental
groups. Histological examination of liver tissue obtained from the hexane-treated
animals demonstrated severe fatty change.
In conclusion, these studies have demonstrated that the isolated liver perfusion technique
is a suitable method of evaluating the effect of therapeutic and supra-therapeutic doses of
some drugs which affect hepatic function.
Ethanol, isoniazid, rifampicin, paracetamol (in therapeutic doses) and hexane were found
to alter liver function as evidenced by impaired gluconeogenesis and bromosulphthalein
clearance. In addition, histological evidence of liver damage was noted in rats treated with hexane. / Thesis (M.Med.Sc.)-University of Natal, Durban, 1988.
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Assessment for evidence of apoptosis of myenteric ganglion cells at the transition zone in Hirschsprung's Disease and the developing large intestineCarter, Terri Anne 20 August 2009 (has links)
Introduction: Hirschsprung’s Disease (HD) is the congenital absence of ganglion cells (GCs) within the distal intestine. Our objectives are to determine if apoptosis of myenteric GCs occurs during human development and to determine if myenteric GC apoptosis or injury contributes to HD.
Materials and Methods: Apoptosis of myenteric GCs was assessed in archived fetal intestinal tissue (n = 4; 15-41 weeks gestational age) and in HD at the transition zone (TZ) (n = 6) using anti-cleaved caspase-3. Immunohistochemistry for GFAP, CD68, HLA-DR and APP was used to assess the presence of enteric reactive changes.
Results: No activated caspase-3 expression was present in the myenteric GCs of the developing human intestine or the TZ of HD. No significant increase in GFAP, CD68, HLA-DR or APP expression was present.
Conclusions: Apoptosis does not appear to occur during the development of the human myenteric plexus or, in conjunction with GC injury, in HD.
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Nutrient absorption from liquid therapeutic diets in an animal modelPoirier, Denise Marie January 1988 (has links)
No description available.
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