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Dive into the research topics where Charis O Hogg is active.

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Featured researches published by Charis O Hogg.


Biology of Reproduction | 2001

Effect of Dietary Energy and Protein on Bovine Follicular Dynamics and Embryo Production In Vitro: Associations with the Ovarian Insulin-Like Growth Factor System

D. G. Armstrong; T.G. McEvoy; G. Baxter; J.J. Robinson; Charis O Hogg; Kathryn J. Woad; R. Webb; Kevin D. Sinclair

Abstract Heifers were assigned either low or high (HE) levels of energy intake and low or high concentrations of dietary crude protein. The effect of these diets on the plasma concentrations of insulin, insulin-like growth factor (IGF)-I, and urea on follicular growth and early embryo development is described. We propose that the observed dietary-induced changes in the ovarian IGF system increase bioavailability of intrafollicular IGF, thus increasing the sensitivity of follicles to FSH. These changes, in combination with increased peripheral concentrations of insulin and IGF-I in heifers offered the HE diet, contribute to the observed increase in growth rate of the dominant follicle. In contrast to follicular growth, increased nutrient supply decreased oocyte quality, due in part to increased plasma urea concentrations. Clearly a number of mechanisms are involved in mediating the effects of dietary energy and protein on ovarian function, and the formulation of diets designed to optimize cattle fertility must consider the divergent effects of nutrient supply on follicular growth and oocyte quality.


Theriogenology | 2002

The effect of increased dietary intake on superovulatory response to FSH in heifers

Jin G. Gong; D. G. Armstrong; G. Baxter; Charis O Hogg; P. C. Garnsworthy; R. Webb

We have previously shown that the number of ovarian follicles <4 mm in diameter can be increased by enhanced dietary intake in heifers. This study investigated the effect of the same dietary treatment on superovulatory response. The estrous cycles of 24 mature Hereford x Friesian heifers were synchronized by a standard progesterone plus prostaglandin protocol. The animals were fed with either 100% (group M, n = 12) or 200% (group 2M, n = 12) maintenance requirements for a 3-week period. Starting from day 4 of the synchronized estrous cycle, all the animals were superovulated using a standard 4-day FSH regime followed by an injection of GnRH analogue (GnRHa) to induce ovulation. Rectal ultrasound scanning was carried out to assess ovarian follicular populations at the start of FSH treatment and on the day of GnRHa injection, and to determine the number of corpora lutea 5 days after GnRHa injection. The body weight (BW) and body condition score (BCS) were recorded weekly and plasma samples were collected throughout the experimental period. There were no differences in either BW or BCS between two groups at the start of the experiment. The BW and BCS were maintained during the experiment in the group M, whilst animals in the group 2M showed a non-significant (P > 0.05) increase in BW and BCS. Circulating concentrations of insulin were significantly (P < 0.01) higher in heifers from the group 2M throughout the controlled feeding period. The group 2M had significantly (P < 0.05) more follicles 2-4 mm in diameter at the start of FSH treatment and more (P < 0.01) follicles >9 mm in diameter on the day of GnRHa injection, when compared with the group M. Similarly, 5 days after GnRHa injection there were significantly (P < 0.01) more corpora lutea in the group 2M (18.1+/-2.2) than in the group M (10.6+/-3.0). In addition, plasma progesterone concentrations following GnRHa injection were significantly (P < 0.01) higher in heifers from the group 2M. In conclusion, these results confirm that increased dietary intake can enhance the recruitment of ovarian follicles in heifers. This treatment may provide a valuable approach to improving superovulatory response in cattle.


Reproduction | 2016

Sex-specific prenatal stress effects on the rat reproductive axis and adrenal gland structure

Cheryl J Ashworth; Susan O George; Charis O Hogg; Yu-Ting Lai; Paula J Brunton

Abstract Social stress during pregnancy has profound effects on offspring physiology. This study examined whether an ethologically relevant social stress during late pregnancy in rats alters the reproductive axis and adrenal gland structure in post-pubertal male and female offspring. Prenatally stressed (PNS) pregnant rats (n=9) were exposed to an unfamiliar lactating rat for 10 min/day from day 16 to 20 of pregnancy inclusive, whereas control pregnant rats (n=9) remained in their home cages. Gonads, adrenal glands and blood samples were obtained from one female and one male from each litter at 11 to 12-weeks of age. Anogenital distance was measured. There was no treatment effect on body, adrenal or gonad weight at 11–12 weeks. PNS did not affect the number of primordial, secondary or tertiary ovarian follicles, numbers of corpora lutea or ovarian FSH receptor expression. There was an indication that PNS females had more primary follicles and greater ovarian aromatase expression compared with control females (both P=0.09). PNS males had longer anogenital distances (0.01±0.0 cm/g vs 0.008±0.00 cm/g; P=0.007) and higher plasma FSH concentrations (0.05 ng/mL vs 0.006 ng/mL; s.e.d.=0.023; P=0.043) compared with control males. There were no treatment effects on the number of Sertoli cells or seminiferous tubules, seminiferous tubule area, plasma testosterone concentration or testis expression of aromatase, FSH receptor or androgen receptor. PNS did not affect adrenal size. These data suggest that the developing male reproductive axis is more sensitive to maternal stress and that PNS may enhance aspects of male reproductive development.


Endocrinology | 1998

Insulin-like growth factor binding protein -2 and -4 messenger ribonucleic acid expression in bovine ovarian follicles: effect of gonadotropins and developmental status.

D. G. Armstrong; G Baxter; C G Gutierrez; Charis O Hogg; A L Glazyrin; B. K. Campbell; T. A. Bramley; R. Webb


Journal of Endocrinology | 2000

Expression of mRNA encoding IGF-I, IGF-II and type 1 IGF receptor in bovine ovarian follicles

D G Armstrong; Carlos G. Gutiérrez; G. Baxter; A L Glazyrin; G.E. Mann; Kathryn J. Woad; Charis O Hogg; R Webb


Reproduction | 2002

Insulin-like growth factor (IGF) system in the oocyte and somatic cells of bovine preantral follicles

D. G. Armstrong; G. Baxter; Charis O Hogg; Kathryn J. Woad


Biology of Reproduction | 1998

Expression of Monocyte Chemoattractant Protein-1 in the Bovine Corpus Luteum Around the Time of Natural Luteolysis

L.A. Penny; D. G. Armstrong; G. Baxter; Charis O Hogg; H. Kindahl; T. A. Bramley; E.D. Watson; R. Webb


Biology of Reproduction | 1996

Insulin-like growth factor (IGF)-binding protein production by primary cultures of ovine granulosa and theca cells. The effects of IGF-I, gonadotropin, and follicle size.

D. G. Armstrong; Charis O Hogg; B. K. Campbell; R. Webb


Domestic Animal Endocrinology | 2004

Expression of messenger ribonucleic acid encoding for steroidogenic acute regulatory protein and enzymes, and luteinizing hormone receptor during the spring transitional season in equine follicles

E.D. Watson; Sung-Eun Bae; Michael G. Steele; Ragnar Thomassen; Hanne G Pedersen; T. A. Bramley; Charis O Hogg; D. G. Armstrong


Theriogenology | 2005

Expression of mRNA encoding insulin-like growth factor binding protein-2 (IGFBP-2) during induced and natural regression of equine corpora lutea

E.D. Watson; Sung-Eun Bae; M.O. Al-zi’abi; Charis O Hogg; D. G. Armstrong

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R. Webb

University of Nottingham

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E.D. Watson

University of Edinburgh

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Sung-Eun Bae

University of Edinburgh

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B. K. Campbell

University of Nottingham

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