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Vioral, ovarian and endocrine relationship in the pubertal bitch. J Anim Sci 1981; 53 1 ; : 182-1. 6. Concannon PW, Hansel W, Visek VJ. The ovarian cycle of the bitch: Plasma estrogen, LH and progesterone. Biol Reprod 1975; 13: 112-21. Concannon PW, Hansel W, McEntee K. Changes in LH, progesterone and sexual behavior associated with preovulatory luteinization in the bitch. Biol Reprod 1977; 17: 604-13. Jones GE, Boyns AR, Cameron EHD, Bell ET, Christie DW, Parkes MF. Plasma estradiol. Luteinizing hormone and progesterone during pregnancy in the Beagle bitch. J Reprod Fertil 1973; 35: 187-9. Olson PN, Bowen RA, Behrendt MD, Olson JD, Nett TM. Concentrations of reproductive hormones in canine serum throughout late anestrus, proestrus and estrus. Biol Reprod 1982; 27: 1196-206. Kooistra HS, Okkens AC, Bevers MM, et al. Concurrent pulsatile secretion of luteinizing hormone and follicle-stimulating hormone during different phases of the estrus cycle and anestrus in beagle bitches. Biol Reprod 1999; 60: 65-71. Concannon PW. Biology of gonadotrophin secretion in adult and prepubertal female dogs. J Reprod Fertil 1993; 47 Suppl ; : 3-27. 12. Phemister RD, Holst PA, Spano JS, Hopwood ML. Time of ovulation on the beagle bitch. Biol Reprod 1973; 8: 74-82. Wildt DE, Chacraborty PK, Panko WB, Seager SWJ. Relationship of reproductive behavior, serum luteinizing hormone and time of ovulation in the bitch. Biol Reprod 1978; 18: 561-70. Holst PA, Phemister RD. The prenatal development of the dog: preimplantation events. Biol of Reprod 1971; 5: 194-206. Okkens AC, Dieleman SJ, Bevers MM, Willemse AH. Evidence of non-involvement of the uterus in the lifespan of the corpus luteum in the cyclic dog. Vet Q 1985; 7: 169-73. Okkens AC, Dieleman SJ, Bevers MM, Lubberink AAME, Willemse AH. Influence of hypophysectomy on the lifespan of the corpus luteum in the cyclic dog. J Reprod Fertil 1986; 77: 187-92. Galac S, Kooistra HS, Dieleman SJ, Cestnik V, Okkens AC. Effects of aglpristone, a progesterone receptor antagonist, administered during the early luteal phase in the non-pregnant bitch. Theriogenology 2003, Submitted. 18. Concannon PW, Weinstein R, Whaeley S, Frank D. Suppression of luteal function in dogs by luteinizing hormone antiserum and bromocriptine. J Reprod Fertil 1987; 81: 175-80. Okkens AC, Bevers MM, Dieleman SJ, Willemse AH. Evidence for prolactin as the main luteotrophic factor in the cyclic dog. Vet Q 1990; 12: 193-201. Onclin K, Verstegen JP. In vivo investigation of luteal function in dogs: effects of cabergoline, a dopamine agonist, and prolactin on progesterone secretion during mid-pregnancy and diestrus. Dom Anim Endocrinol 1997; 14: 25-38. Onclin K, Verstegen JP, Concannon PW. Timerelated changes in canine luteal regulation: in vivo ef and
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Prevention of weight gain.--Because we do not appear to have much success in getting those who are overweight to maintain weight loss over the long term, it is important to put emphasis on developing methods and policies to prevent weight gain in the first place. Issues related to diet and exercise.--Finally, other crucial research would include: comparative studies examining gender, ethnicity, age, and socioeconomic status to disclose biological differences and, equally important, to identify some of the barriers to adopting new lifestyles; studies evaluating the relative impacts on cardiovascular risk of isocaloric, low-fat diets, and hypocaloric diets among both lean and overweight people with mild-to-moderate levels of hypercholesterolemia; assessing the role of subtypes of fat, dietary glycemic index, and dietary fiber on vascular risk factors; establishing the importance of the frequency and size of meals, two factors that influence insulin resistance; and investigating the frequency and intensity of exercise in terms of their relationship with blood pressure, lipid levels, and carbohydrate metabolism. Recommendations on Methodologic Approaches Improved measurements of caloric intake and energy expenditure.--Because of the imprecision involved in measuring caloric intake and energy expenditure, studies have often used weight loss as a more objective measure. Better instruments are needed to measure both these parameters; further, these instruments need to be practical and made available for use in epidemiologic studies where large numbers of subjects are likely to be involved. Special attention should be given to developing and validating methods to assess diet and physical activity over the adult years that will characterize patterns of diet and physical activity over this period. This will then enable categorizing the phenotype of individuals who remain weight stable over most of their adult years into those who achieve this phenotype by decreasing caloric intake and those who may balance a higher caloric intake with greater physical activity. Development of better weight reduction techniques.-- Another important avenue of exploration is the development of weight reduction methods, including pharmaceutical interventions, with higher levels of effectiveness. Many weight loss trials have high drop-out rates in both intervention and control arms. Improving compliance over long periods is a challenge that must be pursued using self-motivation and other psychological intervention tools. Use of surrogate endpoints for the aging process.-- We need to develop better surrogate endpoints for the aging process. Atherosclerosis may not be a good marker, as the prevalence of atherosclerosis is low in some populations of older individuals. Among the surrogate endpoints that might be appropriate for investigation are renal function e.g., glomerular filtration rate ; , vascular stiffness, oxidative stress, glycation products, levels of interleukin-6, or tumor necrosis factor alpha. Further details are provided in the reports of other panels and clindamycin.
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