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IN-DEPTH: REPRODUCTIVE ENDOCRINOLOGY


rise in late pregnancy and help maintain uterine quiescence up until just before parturition.8,9 In normal pregnancies, progestogens actually upregu- late a placental enzyme, 15-hydroxy prostaglandin dehydrogenase that breaks down prostaglandins. Prostaglandin F will cause smooth muscle contrac- tion. Thus, it is postulated that higher progesto- gens lower the effects of prostaglandins and quiet the myometrium.9 In addition, progestogens have immune modulating effects critical for pregnancy maintenance.30 Although exogenous progestins were shown to


in the foal at birth.33 A recent study compared parturition and foal health parameters in normal pony mares maintained on the 0.088 mg/kg dose of altrenogest through foaling and those that were not administered altrenogest. In six healthy pony mares supplemented with altrenogest through par- turition, stage II active labor was more than 10 minutes in duration in four of the five treated mares, and one additional treated mare required a cesarean section. Foals from treated mares had lower respi- ratory rates and higher blood pH; one foal died at 30 minutes, and another needed intensive supportive care.34 Finally, these researchers found that there were differences in the neutrophil-to-lymphocyte ra- tio, suggesting dysmaturity, in foals born to altreno- gest-treated pony mares.35 Some progestins have been shown to alter mental arousal status. When progesterone was adminis- tered systemically to pregnant ewes, fetal lamb mental status was lessened as determined by mon- itoring of fetal neurologic and electromyographic re- sponses.36 Regarding its effect in horses, one case report describes a foal that became stuporous and obtunded after being administered the progesterone metabolite allopregnanolone.37 However, it is cur- rently not known if administration of progestins to the pregnant mare causes any noticeable altera- tion in fetal mental status. Interestingly, proges-


be effective in maintaining early pregnancy in the face of attempted cloprostenol-induced abortion,19 similar studies have not been performed in late pregnancy. However, the efficacy of progestin treatment has been demonstrated when used in combination with trimethoprim sulfamethoxazole (30 mg/kg, q 12 h, PO) and pentoxifylline (8.5 mg/kg, q 12 h, PO) to treat experimentally induced bacterial placentitis.31 Altrenogest at a dose of 0.088 mg/kg (q 24 h, PO; “double dose”) was used in both the placentitis31 and cloprostenol studies.19 Regarding the safety of supplemental progestogen administration, safety studies presented on the al- trenogest labela indicate that the only untoward sign was increased clitoral size in fillies born to normal mares that were administered 0.088 mg/kg (q 24 h, PO), beginning at 20 days of gestation and ending at 325 days.32 Thus, it seems reasonable to discontinue altrenogest by approximately 325 days of gestation. Altrenogest crosses the placenta and is present


terone therapy has been used in humans with acute traumatic brain injury, in which case the proges- terone is thought to have neuro-protective effects and to lessen cerebral edema.38 Additionally, a ro- dent model of pediatric brain trauma with the use of progesterone as a treatment has shown some pos- itive neuro-protective effects.39 Finally, human pediatric studies evaluating progesterone treat- ment effectiveness in head trauma are planned or ongoing.40,41 Another consideration is whether administration


of progestogens to the late-gestation pregnant mare can alter gestational length. Progestogens rise near term and then fall off precipitously in the last 1 to 2 days before foaling.1,2 If progestogens are administered to the late-pregnant mare, could this treatment mimic what is happening in late gesta- tion and inadvertently shorten gestational length? Only a few studies have addressed this pertinent question. When natural progesterone was admin- istered daily to healthy mares from 318 days of gestation to foaling, gestational length was short- ened from a mean of 344 days in nine untreated controls to a mean of 332 days in the nine treated mares.42 Reportedly, these foals were healthy at birth.42 As discussed above, six healthy, late- gestation pony mares were administered a double dose of altrenogest through foaling. The gesta- tional length of ponies administered altrenogest tended to be shorter but was not statistically sig- nificant from the untreated controls.34 Finally, groups of six pregnant pony mares were admin- istered either altrenogest, progesterone, or placebo daily from 300 days of gestation for 10 days.13 Gestational length was not different between groups, and all foals were reportedly healthy. In this study, progesterone supplementation increased total progestogens as measured in the mare serum, but altrenogest did not increase total progesto- gens.13 With such small sample sizes, the possibil- ity of normal gestational length variability negating any effects between groups might be considered. Additionally, if one considers that equine gestation is normally variable between 320 to 365 days, then there is the chance that progestin administration did nothing to shorten gestation in early studies. Nevertheless, the administration of progesterone or altrenogest did not reliably prevent equine parturition. Limited work has been performed looking at the administration of estrogens to the pregnant mare. In one study,25 clinical cases of mares assumed to have placentitis and medically managed with vari- ous antibiotic and medical regimens were either ad- ministered no estrogens or either estrogen cypionate or estradiol 17. The mares were not administered progestins. The live foal rate of 70% was higher in the group given either of the two estrogen prepara- tions compared with the live foal rate of 20% in mares not given estrogen. In this study, the live foal rate was 87% for a control group of normal


AAEP PROCEEDINGS  Vol. 59  2013 355


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