No description available.

No description available.

Thesis (Ph.D.) -- University of Adelaide, School of Paediatrics and Reproductive Health, Discipline of Obstetrics and Gynaecology, 2008. / Includes Errata sheet attached to inside back page (page numbered as 191). Bibliography: leaves 169-187. Also available in print form.

Circadian rhythms are the endogenous cycling of hormones, activity patterns and gene expression that occur across 24 hours. Disruption of circadian rhythms has been associated with multiple health complications, including reduction of fertility. The bmal1 mouse provides an animal model for central and peripheral loss of rhythmicity. Herein the reproductive function and postnatal development in the bmal1 knockout mouse has been evaluated. The reproductive capability of the heterozygous breeding colony was investigated, with around 50% of the female breeder mice becoming pregnant within one estrus cycle. The offspring of the colony had a higher than expected level of perinatal mortality while the knockout and heterozygous genotype was under represented among the offspring surviving to weaning, suggesting high knockout embryo or perinatal losses. The circadian phenotype of this mouse model was confirmed, identifying the severe disruption of circadian behavioural rhythms. Further, the growth of the bmal1 knockout mice was retarded compared with their heterozygous and wild type littermates from weaning to 9 months of age. The reproductive function of the homozygous male bmal1 knockout mouse was evaluated. They showed poor fertility, poorly developed secondary sexual organs, reduced sperm count and reduced sperm motility. Female bmal1 knockout mice had delayed vaginal opening, delayed onset of first estrus, disrupted estrus cyclicity as well as impaired reproductive and mammary tissue development. Steroid hormone synthesis was compromised in both males (testosterone) and females (progesterone) and ovarian morphology revealed reduced corpora lutea formation and structural abnormalities. Female bmal1 knockout mice also evidenced profound infertility, which was caused by a continuum of reproductive insufficiencies including reduced ovulation of oocytes, poorer progression of the preimplantation embryo and failure to successfully implant in the uterus. While the ovaries of bmal1 knockout females were able to respond to exogenous stimulation, the number of ovulated oocytes was reduced, the fertilised oocytes were of reduced quality, progressed poorly to mature blastocyst and once again failed to implant. A bioinformatical evaluation of a panel of genes closely involved in reproduction and ovarian function was analysed for the presence of circadian enhancer regions (E-box sequences) or RORA response elements (RRE) in their promoter regions. It was revealed that many of the genes investigated contained one or more circadian E-box and RRE sequence, providing a mechanism for the disruption of circadian gene expression within the ovary to cause detrimental changes in gene expression. Further to this, the gene expression profile of these functional genes and clock genes were evaluated in ovarian tissues from wild type and knockout mice across the estrus cycles and across 24 hours. It was shown that the murine ovary rhythmically expressed the genes involved with the molecular clock across 24 hours, as well as several other genes previously associated with rhythmicity in peripheral tissues. Further, the loss of functional bmal1 gene expression resulted in up or down regulation of over 75% of the functional genes investigated, including steroidogenic acute regulatory protein (the rate limiting enzyme for progesterone synthesis). In conclusion, the bmal1 knockout mouse shows a significant multi-factorial loss in fertility in both males and females. This loss occurs across a range of tissues and results in heavily reduced fertility in the male and complete infertility in the female. Further research could identify in greater detail the precise molecular mechanisms underpinning of this disruption. / Thesis (Ph.D.) -- University of Adelaide, School of Paediatrics and Reproductive Health, 2008

No description available.

The aim of this diploma thesis was to assess the performance achieved at sows of CLW breed and hybrid sows of CLW x CL within 1 year in a selected breeding. As a result of the appearance of heterosis effect, 0.34 of live born piglets more was born at the cross breeds of F1 generation CLW x CL than to the sows of the CLW breeds. The sows with the length of pregnancy up to 114 days (11.34 piglets) delivered by 0.62 live-born piglets more than sows with the length of pregnancy over 115 days (10.72 piglets). The sows with farrowing interval up to 162 days had a higher number of live-born piglets (11.54) than the sows with farrowing interval over 163 days (11.39). The mating of the sows the fifth day after the piglet weaning, had a positive effect on the number of live-born piglets. The effect of age at first mating on the number of live-born piglets was positively reflected in the interval age 256?270 days (10.53 pieces) and 210?225 days (10.47 pieces). The highest number of live-born piglets was demonstrated from 3rd to 5th parity. The most sows of both genotypes were selected because of returning to service. The analysis of an age structure of the herd was performed as well.

<p>Camellia sinensis (tea) and Aspalathus linearis (rooibos) may improve reproductive function owing to their antioxidant properties. To test this<br /> hypothesis, male and female rats were given 2% and 5% green tea (Gt), black tea (Bt), unfermented rooibos (Ur) or fermented rooibos (Fr) as sole source of drinking for 52 and 21 days respectively. Control rats received tap water. In addition, TM3 Leydig cells were exposed to 0.025, 0.05, 0.1 and 0.5 % aqueous extracts of green tea, black tea, unfermented and fermented rooibos for 24h. In vitro analysis of tea and the herbal infusion revealed the phenolic property and antioxidant capacity (FRAP) in the order Gt &gt / Bt &gt / Ur &gt / Fr. Camellia sinensis and Aspalathus linearis revealed no significant effect on serum antioxidant capacity (p &gt / 0.05) and lipid peroxidation (MDA) in the kidney or liver in both male and female rats and in the testes of the male rats (p &gt / 0.05). In addition, the antioxidant levels were maintained in the testes, liver and kidneys in both the male and female rats. In the male rats, no significant alterations were observed in body weight gain, liver and reproductive organs weight, and serum testosterone (p &gt / 0.05). Only, 5% green tea significantly increased testosterone level (p &lt / 0.05). Seminiferous tubules displayed complete spermatogenesis with abundant sperm in the lumen in all treated groups. However, a significant decrease in diameter and germinal epithelial height of these tubules were observed (p &lt / 0.05). In the epididymides, epithelial height of caput region showed a significant increase (p &lt / 0.01), while the cauda region was increased by Camellia sinensis but decreased by Aspalathus linearis. Sperm concentration improved significantly by green tea and unfermented rooibos (p &lt / 0.05), while black tea and fermented rooibos produced a non significant effect (p &gt / 0.05). Sperm viability was enhanced in all treatment groups (p &lt / 0.05). Furthermore, green tea, black tea and unfermented rooibos significantly improved the motility of rat sperm (p &lt / 0.05) / fermented rooibos tended to improve it (p &gt / 0.05). In addition, green tea, black tea and fermented rooibos enhanced acrosome reaction (p &lt / 0.05). Creatinine activity was significantly higher in rats treated with black tea, unfermented rooibos or fermented rooibos (p &lt / 0.05), green tea tended to increase it (p &gt / 0.05) reflecting the significant increased kidney weight in the treatment groups at high concentrations. Liver markers, ALT and AST, decreased significantly in all treated groups (p &lt / 0.05), except in 5% fermented rooibos where a significant increase in AST level was observed (p &lt / 0.01). In the female rats, the body weight gain, and reproductive organs weight was no affected (p &gt / 0.05). However, 5% fermented rooibos reduced the ovarian weight (p &lt / 0.05), while 5% unfermented rooibos significantly increased the uterine weight (p &lt / 0.05). Liver weight increased significantly by black tea and unfermented rooibos (p &lt / 0.05) while the kidney weight increased significantly by 5% black tea (p &lt / 0.05). No significant effect was observed in the level of FSH produced, on the other hand, Camellia sinensis significantly lowered the level of LH (p &lt / 0.05), while Aspalathus linearis had no effect (p &gt / 0.05). Creatinine activity was enhanced significantly only by 5% fermented rooibos (p &lt / 0.05). Liver markers, ALT and AST were reduced in most treated groups except in fermented rooibos where an increase was observed. In addition, histological sections revealed no obvious alteration in the ovaries, uteri, kidneys and liver of all treated female rats. Camellia sinensis and Aspalathus linearis significantly reduced the level of testosterone produced in TM3 Leydig cells under stimulated conditions in vitro (p&lt / 0.05). Furthermore, both plants maintained the viability and morphology of the cells. However, at 0.5% of either plant extracts, a significant decrease in the viability (p &lt / 0.05) and altered morphology of the TM3 Leydig cells was observed. In conclusion, Camellia sinensis and Aspalathus linearis significantly improved certain sperm function which might be attributed to their high level of antioxidant activity. However, the prolonged exposure of both plant extracts might result in subtle structural changes in the male reproductive system and impair kidney function. In addition, fermented rooibos at high concentration may also impair the functions of the liver. In vitro, both plants were shown to possess anti-androgenic property on TM3 Leydig cells. Furthermore, both Camellia sinensis and Aspalathus linearis may be classified as weak phytoestrogens due to the changes in the weight of the uterus and ovaries observed.</p>

<p>Camellia sinensis (tea) and Aspalathus linearis (rooibos) may improve reproductive function owing to their antioxidant properties. To test this<br /> hypothesis, male and female rats were given 2% and 5% green tea (Gt), black tea (Bt), unfermented rooibos (Ur) or fermented rooibos (Fr) as sole source of drinking for 52 and 21 days respectively. Control rats received tap water. In addition, TM3 Leydig cells were exposed to 0.025, 0.05, 0.1 and 0.5 % aqueous extracts of green tea, black tea, unfermented and fermented rooibos for 24h. In vitro analysis of tea and the herbal infusion revealed the phenolic property and antioxidant capacity (FRAP) in the order Gt &gt / Bt &gt / Ur &gt / Fr. Camellia sinensis and Aspalathus linearis revealed no significant effect on serum antioxidant capacity (p &gt / 0.05) and lipid peroxidation (MDA) in the kidney or liver in both male and female rats and in the testes of the male rats (p &gt / 0.05). In addition, the antioxidant levels were maintained in the testes, liver and kidneys in both the male and female rats. In the male rats, no significant alterations were observed in body weight gain, liver and reproductive organs weight, and serum testosterone (p &gt / 0.05). Only, 5% green tea significantly increased testosterone level (p &lt / 0.05). Seminiferous tubules displayed complete spermatogenesis with abundant sperm in the lumen in all treated groups. However, a significant decrease in diameter and germinal epithelial height of these tubules were observed (p &lt / 0.05). In the epididymides, epithelial height of caput region showed a significant increase (p &lt / 0.01), while the cauda region was increased by Camellia sinensis but decreased by Aspalathus linearis. Sperm concentration improved significantly by green tea and unfermented rooibos (p &lt / 0.05), while black tea and fermented rooibos produced a non significant effect (p &gt / 0.05). Sperm viability was enhanced in all treatment groups (p &lt / 0.05). Furthermore, green tea, black tea and unfermented rooibos significantly improved the motility of rat sperm (p &lt / 0.05) / fermented rooibos tended to improve it (p &gt / 0.05). In addition, green tea, black tea and fermented rooibos enhanced acrosome reaction (p &lt / 0.05). Creatinine activity was significantly higher in rats treated with black tea, unfermented rooibos or fermented rooibos (p &lt / 0.05), green tea tended to increase it (p &gt / 0.05) reflecting the significant increased kidney weight in the treatment groups at high concentrations. Liver markers, ALT and AST, decreased significantly in all treated groups (p &lt / 0.05), except in 5% fermented rooibos where a significant increase in AST level was observed (p &lt / 0.01). In the female rats, the body weight gain, and reproductive organs weight was no affected (p &gt / 0.05). However, 5% fermented rooibos reduced the ovarian weight (p &lt / 0.05), while 5% unfermented rooibos significantly increased the uterine weight (p &lt / 0.05). Liver weight increased significantly by black tea and unfermented rooibos (p &lt / 0.05) while the kidney weight increased significantly by 5% black tea (p &lt / 0.05). No significant effect was observed in the level of FSH produced, on the other hand, Camellia sinensis significantly lowered the level of LH (p &lt / 0.05), while Aspalathus linearis had no effect (p &gt / 0.05). Creatinine activity was enhanced significantly only by 5% fermented rooibos (p &lt / 0.05). Liver markers, ALT and AST were reduced in most treated groups except in fermented rooibos where an increase was observed. In addition, histological sections revealed no obvious alteration in the ovaries, uteri, kidneys and liver of all treated female rats. Camellia sinensis and Aspalathus linearis significantly reduced the level of testosterone produced in TM3 Leydig cells under stimulated conditions in vitro (p&lt / 0.05). Furthermore, both plants maintained the viability and morphology of the cells. However, at 0.5% of either plant extracts, a significant decrease in the viability (p &lt / 0.05) and altered morphology of the TM3 Leydig cells was observed. In conclusion, Camellia sinensis and Aspalathus linearis significantly improved certain sperm function which might be attributed to their high level of antioxidant activity. However, the prolonged exposure of both plant extracts might result in subtle structural changes in the male reproductive system and impair kidney function. In addition, fermented rooibos at high concentration may also impair the functions of the liver. In vitro, both plants were shown to possess anti-androgenic property on TM3 Leydig cells. Furthermore, both Camellia sinensis and Aspalathus linearis may be classified as weak phytoestrogens due to the changes in the weight of the uterus and ovaries observed.</p>