ABSTRACT. In a cow diagnosed as having ovarian cysts, we observed changes in the ovarian structures by ultrasonography for 71 days and examined plasma concentrations of sex hormones. The cow had 2 regressing cysts at the start of this study and 3 new follicles subsequently developed into cysts. With regression of these cysts, 2 new follicles developed and ovulated spontaneously, followed by the formation of 2 corpora lutea. On the day prior to ovulation, a preovulatory luteinizing hormone (LH) surge was detected. With regression of the corpora lutea, a new follicle developed and underwent atresia. Meantime, another follicle developed and became a cyst without ovulation. No preovulatory LH surge was observed during the period from regression of the corpora lutea to cyst formation. The results indicate that absence of the preovulatory LH surge is associated with occurrence of ovarian cysts and this endocrine aberration is reversible. -KEY WORDS: cattle, LH surge, ovarian cyst.J. Vet. Med. Sci. 60(2): 257-260, 1998 Follicular and luteal structures were examined by transrectal ultrasonography using a 5 MHz transducer and linear-array ultrasound scanner (SSD-280, Aloka, Tokyo, Japan) by the method previously described by Pierson and Ginther [13], and rectal palpation was performed to monitor ovarian changes. At each examination, follicles with a diameter exceeding 10 mm and the location of each structure were recorded on an ovarian map. Ultrasonic examination was made at 3 day intervals. When the cysts or corpora lutea regressed, however, and new follicular structures grew from 10 mm to more than 25 mm in diameter or to ovulation, examination was made daily for 2 series.Blood samples were collected by jugular venipuncture into heparinized vacutainers at 2 day intervals following the start of ultrasonic examination. An indwelling jugular cannula was used for sampling, when the ovaries were examined daily. All samples were collected between 8:00 and 9:30 hr. The samples were kept on ice and centrifuged at 1,500 g for 30 min at 4°C within 30 min. Plasma was collected and stored at 20°C until the concentrations of LH, follicle-stimulating hormone (FSH), progesterone and estradiol-17β were measured. Additional blood samples were collected via the jugular cannula into plain vacutainers at 3 hr intervals following the start of daily examinations of the ovaries to determine the presence of a preovulatory LH surge. After collection, the samples were kept for 6-18 hr at room temperature. Serum was separated by centrifugation and stored at 20°C until the concentrations of LH were measured.Plasma and serum concentrations of LH were measured by the homologous double-antibody radioimmunoassay (RIA) method described previously [8] using anti-bovine LH serum (i555/001, UCB-Bioproducts, Braine-l'Alleud, Belgium), bovine LH (i055, UCB-Bioproducts) for radioiodination, and LER-1716-2 (provided by Dr. L. E. Reichert, Albany Medical College) as a reference standard. Plasma concentrations of FSH were measured by RIA [2] using anti-bovi...