Noninvasive monitoring of ovarian endocrine activity in the chinchilla (Chinchilla lanigera).

Reproductive endocrinology information is limited for Chinchilla lanigera, a South American species characterized by extremely long gestation and estrus cycle compared with others rodents. This study was designed to validate a non-invasive technique for monitoring ovarian endocrine activity. Animals were exposed indoors to natural photoperiod (31 degrees S-64 degrees W, Argentina); temperature range: 17-26 degrees C, with food and water ad libitum. Radiolabelled infusion (n=4): (3)H-estradiol ((3)H-E(2)) and (14)C-progesterone ((14)C-P(4)) were injected (i.p). Biochemical validation: HPLC-UV detector was employed to determine natural steroids in urine and fecal extracts and to determine immunoreactive metabolites. Physiological validation: (1) pregnancy (n=5): body weight and urinary and fecal steroidal metabolites were measured until birth; (2) Seasonality (n=9): urine and feces were collected in May, August, November, and February. Total (3)H-E(2) and (14)C-P(4) radioactivity recovered was 60.5+/-15.5 and 74.5+/-19.4%, respectively. After (3)H-E(2) injection, urinary radioactivity peaked at 7.0+/-0.6 hr; in contrast, urinary (14)C-P(4) excretion peaked at 44.0+/-4.0 hr (p=0.000). Peak radioactivity in feces occurred between 24-48 hr for both hormones. Several correlations were detected during pregnancy between body weight vs. urinary progestagens/day (r=0.44, p<0.03); vs. urinary progestagens/creatinine (r=0.73, p=2.9 x 10(-5)); vs. urinary estrogens/day (r=0.74; p<0.2); and vs. urinary estrogens/creatinine (r=0.74; p<2.0 x 10(-5)). On the other hand, urinary and fecal progestagen excretion exhibited significant seasonal fluctuations and urinary estrogen concentrations showed a similar pattern (p=0.062 for winter-spring vs. summer-autumn). This methodology proved to be useful for monitoring ovary endocrine activity in urine of chinchilla female.