Influence of l-arginine supplementation on reproductive blood flow and embryo recovery rates in mares

التفاصيل البيبلوغرافية
العنوان: Influence of l-arginine supplementation on reproductive blood flow and embryo recovery rates in mares
المؤلفون: M. M. Leblanc, Dale E. Kelley, Lori K. Warren, C.J. Mortensen
المصدر: Theriogenology. 81:752-757
بيانات النشر: Elsevier BV, 2014.
سنة النشر: 2014
مصطلحات موضوعية: Ovulation, endocrine system, medicine.medical_specialty, medicine.medical_treatment, media_common.quotation_subject, Hemodynamics, Luteal phase, Biology, Arginine, Insemination, Follicle, Ovarian Follicle, Food Animals, Pregnancy, Internal medicine, Follicular phase, medicine, Animals, Horses, Small Animals, Insemination, Artificial, Ultrasonography, media_common, Equine, Reproduction, Artificial insemination, Ovary, Arteries, Embryo, Mammalian, Endocrinology, Dietary Supplements, Tissue and Organ Harvesting, Female, Vascular Resistance, Animal Science and Zoology, Perfusion
الوصف: Supplementation with L-arginine can increase uterine arterial blood flow and vascular perfusion of the preovulatory follicle in mares. Increased vascular perfusion of the preovulatory follicle has been correlated with successful pregnancy in mares. The objective of this study was to determine if supplemental L-arginine would increase ovarian arterial blood flow, vascular perfusion of the preovulatory follicle, and embryo recovery rates in mares. Mares were blocked by age and breed and assigned at random within block to L-arginine supplementation or control groups. Mares were fed L-arginine beginning 17 days before and through the duration of the study. Transrectal Doppler ultrasonography was used to measure ovarian arterial blood flow and vascular perfusion of the preovulatory follicle daily when it reached 35 mm and subsequent CL on Days 2, 4, and 6. Mares, on achieving a follicle of 35 mm or more were bred via artificial insemination and an embryo collection was attempted 7 days after ovulation. Treatment did not affect interovulatory interval (arginine-treated, 18.1 ± 2.6 days; control, 20.7 ± 2.3 days) or embryo recovery rate (arginine-treated, 54%; control, 48%). Mares treated with l-arginine had a larger follicle for the 10 days preceding ovulation than control mares (30.4 ± 1.2 and 26.3 ± 1.3 mm, respectively; P < 0.05) and vascular perfusion of the dominant follicle tended (P = 0.10) to be greater for the 4 days before ovulation. No differences were observed between groups in diameter or vascular perfusion of the CL. Resistance indices, normalized to ovulation, were not significantly different between groups during the follicular or luteal phase. Oral l-arginine supplementation increased the size and tended to increase perfusion of the follicle 1, but had no effect on luteal perfusion or embryo recovery rates in mares.
تدمد: 0093-691X
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89485aad629008d04752c7860453e1c1
https://doi.org/10.1016/j.theriogenology.2013.12.012
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....89485aad629008d04752c7860453e1c1
قاعدة البيانات: OpenAIRE