Spelling suggestions: "subject:"sheep -- physiology"" "subject:"sheep -- hophysiology""
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The effect of supplementation of alfalfa hay or urea on intake digestibility and rumen fermentation of sheep fed timothy hay /Delaquis, Annick Marie January 1987 (has links)
No description available.
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Lutalyse® induces uterine-ovarian PGF₂α release in sheep: a critical component of induced luteolysisWade, Dawn E. 21 July 2009 (has links)
Exogenous PGF<sub>2α</sub>, (see Appendix I for definitions of abbreviations) is luteolytic in midluteal (1.e., d 9 of a 17 d estrous cycle) sheep. However, the pharmacokinetic responses to PGF<sub>2α</sub>-induced luteolysis are not known. This study (Exp. 1 and 2) was conducted to determine several pharmacokinetic responses to two dosing regimens of Lutalyse® (PGF<sub>2α</sub>). Experiment 1 was a 2 x 2 factorial design, with Lutalyse and H/Ox as main effects. Lutalyse (15 mg) was injected i.m., and blood samples were collected, relative to the time of injection, from the vena cava at points cranial and caudal to the uteroovarian vein. Progesterone and PGF<sub>2α</sub>, were measured in blood plasma. The PGF<sub>2α</sub> concentrations were greater in H/Ox and sham H/Ox ewes treated-with Lutalyse® than in control ewes. Peak concentrations of PGF<sub>2α</sub> were greatest in sham H/Ox Lutalyse-treated ewes, indicating that the uterus and(or) ovaries secrete PGF<sub>2α</sub>, in response to exogenous PGF<sub>2α</sub>. In Lutalyse-treated ewes, progesterone concentrations decreased by 50% within 8 h after treatment. The design of Exp. 2 was also a 2 x 2 factorial, with Lutalyse (2 x 5mg at 3 h intervals) and H/Ox as main effects. Prostaglandin F<sub>2α</sub> and PGFM were measured in blood plasma collected, relative to the time of injections, from the vena cava at points cranial and caudal to the uteroovarian vein. The PGF<sub>2α</sub> concentrations were greater in sham H/Ox ewes treated-with Lutalyse than in control ewes. Peak concentrations of PGF<sub>2α</sub> were greater in sham H/Ox than in ewes in all other treatment groups, indicating again that the uterus and(or) ovaries secrete PGF<sub>2α</sub> in response to exogenous PGF<sub>2α</sub> In general, PGFM concentrations increased in a pattern similar to that of PGF<sub>2α</sub> after Lutalyse injection; although there was a short delay of approximately 2 min. Caudal vena caval PGF, concentrations in H/Ox Lutalyse-treated ewes were greater than that after saline injection, which indicates that metabolism may depend on the presence or absence of the uterus and(or) ovaries. In Exp. 1, caudal PGF, concentrations were greater in H/Ox ewes injected with 15 mg of Lutalyse than in ewes in all other treatments . However, in response to 5 mg Lutalyse, caudal PGF<sub>2α</sub> concentrations were greater in sham H/Ox ewes than in all other treatment groups. This indicates that the larger dose in H/Ox ewes supersedes the capacity of the lung and kidney to dispose of PGF<sub>2α</sub>, and PGF<sub>2α</sub> is more tightly regulated in intact ewes. The lungs and kidney are capable of metabolizing the smaller dose of Lutalyse but not the resulting PGF<sub>2α</sub> production in intact ewes.
A short validation experiment was conducted to determine the effects of sampling location on progesterone, PGF<sub>2α</sub> and PGFM concentrations. Sampling location did not affect the mean concentration of progesterone or PGFM. However, location affected the mean PGF<sub>2α</sub> concentration. The concentration of PGF<sub>2α</sub>, was greater (P < .05) in saphenous vein and caudal vena caval blood plasma than in jugular plasma.
In summary, the uterus and(or) ovaries produce and regulate PGF<sub>2α</sub> concentration in response to Lutalyse. It is speculated that a threshold PGF<sub>2α</sub> concentration or duration of the PGF<sub>2α</sub> peak concentration exists because these PGF<sub>2α</sub>, responses differed in intact Lutalyse-treated and saline-treated ewes in both experiments. The mean cranial PGF<sub>2α</sub> concentration, peak concentration, duration of the peak, increase in PGF<sub>2α</sub> and AUC were greater in response to 15 mg of Lutalyse, although the two smaller doses have been shown to be more efficacious in inducing luteolysis. The second dose of PGF<sub>2α</sub> may act by mimicking pulses of PGF<sub>2α</sub> and initiate the luteolytic cascade two times. / Master of Science
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Comparison of two CYP17 isoforms : implications for cortisol production in the South African MerinoHough, Denise 03 1900 (has links)
Thesis (PhD)--Stellenbosch University, 2012. / ENGLISH ABSTRACT: This study describes:
• the comparison of the enzymatic activities of the two ovine cytochrome P450 17 -
hydroxylase/17,20-lyase (CYP17) isoforms expressed in non-steroidogenic COS-1 cells.
The Km and Vmax values for the metabolism of pregnenolone and progesterone were
determined, while time-dependent metabolism of pregnenolone, 17-hydroxypregenolone,
progesterone and 17-hydroxyprogesterone was also reported. The cloning and sequencing of
ovine cytochrome b5 is reported and was co-expressed with CYP17. The results showed that
the wild type 1 (WT1) isoform of ovine CYP17 produce more cortisol precursors than the
wild type 2 (WT2) isoform;
• the analysis of the frequency distribution of the CYP17 genotypes within a South African
Merino population, which were divergently selected for (H-line) or against (L-line) the
ability of a ewe to rear multiple offspring per birthing opportunity. It was observed that the
CYP17 frequency distribution was the same within the H- and L-line, with 78.3 %
heterozygous WT1/WT2 and 21.7 % homozygous WT1/WT1. No homozygous WT2/WT2
individuals were identified;
• the development of a UPLC-MS/MS method for the separation and quantification of all
thirteen adrenal steroids that are produced in the adrenal gland;
• the relative contribution of the CYP17 genotypes in the total steroidogenic output in adult
adrenocortical cells from the adrenal glands of H- and L-line sheep, with particular emphasis
on cortisol production. The adrenocortical cells from the H-line sheep showed a marked
higher cortisol production than the L-line, while adrenocortical cells from homozygous
WT1/WT1 sheep also produced more cortisol than heterozygous WT1/WT2 sheep;
• the blood cortisol responses upon the stimulation of the HPA axis by insulin induced
hypoglycaemia of the H- and L-line sheep with known CYP17 genotypes. It was observed
that the CYP17 genotype and selection line are important factors affecting the cortisol
responses of sheep, where L-line heterozygous WT1/WT2 sheep showed the lowest cortisol
response and glucose recovery; • the association of the CYP17 genotype with behavioural responses of H- and L-line sheep to
flock isolation stress, as well as the association of the CYP17 genotype with ewe
reproduction and lamb output. While reproduction seemed to be unaffected by the CYP17
genotype, the behavioural stress responses of sheep to flock isolation correlated with the
CYP17 genotype, where the heterozygous WT1/WT2 genotype was associated with a wilder
nature. / AFRIKAANSE OPSOMMING: Hierdie studie ondersoek:
• die vergelyking van die ensiemaktiwiteite vir twee isoforme van skaap sitochroom P450
17 -hidroksilase/17,20-liase (CYP17), wat uitgedruk was in nie-steroïed genererende COS-
1 selle. Die Km and Vmax waardes was bepaal vir die metabolisme van pregnenoloon en
progesteroon, terwyl die tyd-afhanklike metabolisme van pregnenoloon, 17-
hidroksiepregnenoloon, progesteroon en 17-hidroksieprogesteroon ook gerapporteer word.
Die klonering en volgorde bepaling van skaap sitochroom b5 was gedoen en gevolglik was
sitochroom b5 saam met CYP17 uitgedruk in COS-1 selle. Die resultate het gewys dat wilde
tipe 1 (WT1) meer voorlopers van kortisol produseer as wilde tipe 2 (WT2);
• die frekwensie distrubusie van die CYP17 genotipes in ‘n Suid-Afrikaanse Merino
populasie, waar skape in teenoorgestelde rigtings geselekteer was vir (H-lyn) of teen (L-lyn)
die vermoë van ‘n ooi om geboorte te gee aan veelvoudige lammers per lamgeleentheid. Die
frekwensie distrubusie van CYP17 was dieselfde in beide die H- en L-lyn, waar 78.3 % van
die populasie heterosigoties WT1/WT2 en 21.7 % homosigoties WT1/WT1 was. Geen
homosigote WT2/WT2 individue was geïdentifiseer nie;
• die ontwikkeling van ‘n UPLC-MS/MS metode vir die skeiding en kwantifisering van al
dertien steroïede wat natuurlik geproduseer word in die bynier van die skaap;
• die relatiewe bydrae van die CYP17 isoforme tot die totale steroïedale uitsette vanuit die
bynier kortex selle, vanaf die byniere van H- en L-lyn skape, waar klem geplaas word op die
produksie van kortisol. Die bynierselle van die H-lyn skape het aansienlik meer kortisol
produseer as die L-lyn, terwyl die bynierselle van die homosigotiese WT1/WT1 skape ook
meer kortisol produseer het as heterosigotiese WT1/WT2 skape;
• die bloed kortisol in reaksie tot die stimulering van die hipotalamus-hipofise-adrenale aksis,
deur insulien geïnduseerde hipoglisemiese stress, in skape van die H- en L-lyne met bekende
CYP17 genotipes. Dit was gevind dat die kortisol reaksie geaffekteer word deur beide die
CYP17 genotipe en seleksie lyn, waar L-lyn heterosigotiese WT1/WT2 skape die minste
kortisol geproduseer het en die stadigste herstel van glukose vlakke getoon het; • die assosiasie tussen die CYP17 genotipe en die gedrags reaksies op trop-isolasie, sowel as
ooi-reproduksie en lamuitset, van die H- en L-lyn skape. Die reproduksie parameters was
onafhanklik van die CYP17 genotipe, terwyl ‘n sterk assosiasie gevind was tussen die
CYP17 genotipe en gedrags reaksies op trop-isolasie. Die heterosigotiese WT1/WT2 skape
het ‘n wilder natuur getoon gedurende trop-isolasie in vergelyking met homosigotiese
WT1/WT1 skape.
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Regulation of wool and body growth : nutritional and molecular approachesBray, Megan. January 2002 (has links) (PDF)
"May 2002" Includes bibliographical references (leaves 148-164) Describes a series of novel experiments designed to enhance our understanding of nutrient utilisation for growth of wool and the whole body.
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IGF transfer from blood to tissue: comparison of IGF-I with analogs that bind poorly to binding proteins, using a vascular perfusion model : a thesis submitted to the University of Adelaide, South Australia, for the degree of Doctor of Philosophy / by Andrew Peter Duncan LordLord, Andrew P.D. (Andrew Peter Duncan) January 1993 (has links)
xxiii, 222 leaves : ill. ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Insulin-like growth factor-I circulates at high concentrations in blood, mainly complexed with IGF-binding proteins. The main objective of the thesis is to determine the general role played by plasma IGF-binding proteins in the regulation of IGF transfer from blood to tissues. / Thesis (Ph.D.)--University of Adelaide, Dept. of Animal Science, 1994
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Regulation of wool and body growth : nutritional and molecular approaches / Megan Bray.Bray, Megan January 2002 (has links)
"May 2002" / Includes bibliographical references (leaves 148-164) / xi, 164 leaves : ill. ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Describes a series of novel experiments designed to enhance our understanding of nutrient utilisation for growth of wool and the whole body. / Thesis (Ph.D.)--University of Adelaide, Dept. of Animal Science, 2002
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Behavioral and physiological responses of ewes to semiconfinement and two nutritional levels in a desert climateGardner, Billy Wayne January 1980 (has links)
No description available.
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Vascularization of the intervertebral disc in pathological conditions / Robert James Moore.Moore, R. J. January 1995 (has links)
Bibliography: leaves 148-160. / xix, 160, [40] leaves, [19] leaves of plates : ill. ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Investigates the process of neovascularization of intervertebral disc components, with ageing and in disease. Establishes the extent of end plate vascularization in the lumbar discs of young normal sheep, and demonstrates that some components of the disc undergo neovascularization in response to physical trauma, possibly as a part of tissue repair response. / Thesis (Ph.D.)--University of Adelaide, Dept. of Pathology, 1996?
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An alternative approach to premature luteal regressionPretorius, Willem S 12 1900 (has links)
Thesis (MSc)--University of Stellenbosch, 2006. / ENGLISH ABSTRACT: Premature luteal regression occurs on average in 30% of superovulated sheep ewes. This phenomenon occurs early in the cycle before the embryo’s can be collected and is a major contributor to failure in embryo transfer programs. This research was done to understand the physiological mechanisms involved.
Chapter two provides a general background of the physiology of natural luteolysis and the maternal recognition of pregnancy. The chapter introduces some new concepts on the topic of cell death and provides a recent literature review on research done on the phenomenon of premature luteal regression. This chapter forms the base of ideas and arguments that follows in the two studies containing new original work in this field.
The research contained in this thesis comprises of two in vivo studies. The first study (Chapter 3) compare premature luteal regression to Prostaglandin F2α (PGF2α) induced regression with emphasis on the changes in levels of the steroid hormones progesterone (P4) and estradiol - 17β (E2-17β) and changes in structure and ultra structure. The following conclusions were made:
1. Premature luteal regression is not merely inadequate luteal support, but indeed early luteal regression, since seasonal influences could merely be nutritional influences, and a definitive increase in P4 were recorded in animals exhibiting the phenomena. 2. Nutritional influences could play a role, but the type and quality of nutrients and mechanism involved, is still unclear.
3. PGF2α-induced regression differs from premature luteal regression in that:
a) The progression of functional and structural regression in PGF2α -induced regression is slower than in premature luteal regression.
b) Regressed corpora lutea do not occur with normal functioning corpora lutea.
4. There is a distinct second E2-17β peak preceding the decline in P4 in animals that exhibits signs of premature luteal regression.
A threshold initiating premature luteal regression was not established.
The second study (Chapter 4) compares the changes in the ovine β estradiol - 17 β receptor (oERβ) between premature luteal regression and PGF2α induced regression. The study concludes that there could be a potential role for oERβ in premature luteal regression.
The findings of these two studies raise some questions about the conventional perception that early release of PGF2α is the cause of premature luteal regression. The thesis concludes in a hypothesis (Chapter 4) explaining the phenomenon. / AFRIKAANSE OPSOMMING: Premature luteale regressie kom gemiddeld in 30% van gesuperovuleerde skaap-ooie voor. Die verskynsel kom vroeg in die siklus voor, voor die embrios gekollekteer kan word, en is een van die belangrikste oorsaake van mislukkings in ‘n embrio-oorplaasingsprogram. Die huidige navorsing poog om die fisiologiese meganismes betrokke by premature luteale regressie te verstaan.
Hoofstuk twee verskaf ‘n algemene agtergrond van die fisiologiese aspekte betrokke by natuurlike luteale regressie en maternale herkenning van swangerskap. Die hoofstuk stel nuwe konsepte voor oor sel afsterwing en verskaf ‘n opgedateerde literatuuroorsig met betrekking tot die navorsing wat in die veld oor die verskynsel gedoen is. Die hoofstuk vorm die basis vir die idees en argumente, wat volg in die twee studies en wat oorspronklike nuwe navorsing bevat oor die onderwerp.
Die navorsing in die tesis bestaan uit twee in vivo studies. Die eerste studie (Hoofstuk 3) vergelyk premature luteale regressie en prostaglandien F2α (PGF2α) ge-induseerde regressie met ‘n klem op die vlakke van die steröiedhormone progesteroon (P4) en estradiol - 17β (E2-17β) en veranderinge in die mikroskopiese struktuur en ultra struktuur van die corpus luteum. Die studie bevind:
1. Premature luteale regressie is nie slegs onvoldoende luteale funksie nie, maar vroë luteale regressie aangesien seisoenale invloede eitlik voedings invloede kan wees en P4 gestyg het in diere waar die verskynsel voorgekom het.
2. Voeding kan ‘n rol speel maar die tiepe en gehalte van die voedingstowwe en die meganismes betrokke is nie duidelik nie.
3. PGF2α - ge-induseerde regressie verskil van premature regressie in dat:
a) Die verloop van funksionele en strukturele regressie is stadiger in PGF2α - ge-induseerde regressie in vergelyking met premature luteale regressie.
b) Corpora lutea wat regressie ondergaan het kom nie voor saam met corpora lutea wat normal voorkom nie.
4. Daar die ‘n duidelike tweede piek van E2-17β gaan die afname in P4 vooraf in diere waar premature regressie voorkom.
5. Daar is nie geslaag om ‘n drempel vas te stel waar premature regressie ge-inisieer word nie.
Die tweede studie vergelyk die veranderinge in estradiol-17β reseptore (oERβ) in die skaap tydens premature luteale regressie en PGF2α geinduseerde regressie. Die studie bevind dat daar ‘n moontlike rol is vir ERβ in premature luteale regressie.
Die bevindinge van die twee studies bevraagteken die konvensionele opvatting dat vroë vrystelling van PGF2α verantwoordelik is vir premature luteale regressie. Die tesis sluit af met ‘n nuwe hipotese om die verskynsel te verduidelik.
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IGF transfer from blood to tissue: comparison of IGF-I with analogs that bind poorly to binding proteins, using a vascular perfusion model : a thesis submitted to the University of Adelaide, South Australia, for the degree of Doctor of PhilosophyLord, Andrew P.D. (Andrew Peter Duncan) January 1993 (has links) (PDF)
Includes bibliographical references (leaves 188-217) Insulin-like growth factor-I circulates at high concentrations in blood, mainly complexed with IGF-binding proteins. The main objective of the thesis is to determine the general role played by plasma IGF-binding proteins in the regulation of IGF transfer from blood to tissues.
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