Hearn C M, Shaw G, Short R V, Renfree M B
Department of Zoology, University of Melbourne, Parkville, Victoria, Australia.
J Reprod Fertil. 1998 May;113(1):151-7. doi: 10.1530/jrf.0.1130151.
The effects of the prolactin inhibiting drug, cabergoline, on pregnant and lactating marsupials were investigated in four species from three diverse families: the tammar wallaby, Macropus eugenii, the quokka, Setonix brachyurus, the brushtail possum, Trichosurus vulpecula, and the fat-tailed dunnart, Sminthopsis crassicaudata. In tammar wallabies, 20 micrograms cabergoline kg-1 injected intramuscularly 1 day before expected birth did not alter the timing of parturition but neonates died within a day of birth, suggesting that the onset of lactation was compromised. During early lactation in tammars (56-69 days post partum), an intramuscular injection transiently retarded growth of the young, although they subsequently survived. This treatment induced reactivation of the quiescent corpus luteum and the blastocyst from diapause, so a new birth occurred 26-27 days later, despite the continued sucking of the young in the pouch. Intramuscular injection during late lactation (166-199 days post partum) apparently suppressed milk secretion since pouch young lost up to 20% of their bodyweight or died within 7 days of treatment. Oral administration of cabergoline had no effect on the growth of the young or on the quiescent corpus luteum and diapausing blastocyst. Quokkas showed similar responses to tammars after treatment in late lactation. Possums and dunnarts were less sensitive to injected cabergoline than the two macropodid species, and possums showed no response to oral administration. The lack of response of these marsupial species to oral cabergoline treatment suggests that accidental ingestion of baits, containing 20 micrograms cabergoline kg-1, used to control introduced eutherian pests such as the red fox, Vulpes vulpes, or the feral cat, Felis cattus, should not affect the reproduction of native marsupials.
帚尾袋鼩、肥尾袋鼩、赤褐袋鼠和短尾矮袋鼠。在赤褐袋鼠中,预计分娩前1天肌肉注射20微克/千克卡麦角林不会改变分娩时间,但新生幼崽在出生后一天内死亡,这表明泌乳开始受到影响。在赤褐袋鼠的早期哺乳期(产后56 - 69天),肌肉注射会暂时减缓幼崽的生长,不过它们随后存活了下来。这种处理使静止的黄体和滞育的胚泡重新激活,因此尽管育儿袋中的幼崽仍在持续吮乳,26 - 27天后还是发生了新的分娩。在哺乳期后期(产后166 - 199天)进行肌肉注射显然抑制了乳汁分泌,因为育儿袋中的幼崽体重减轻了多达20%,或者在治疗后7天内死亡。口服卡麦角林对幼崽的生长以及静止的黄体和滞育的胚泡没有影响。短尾矮袋鼠在哺乳期后期接受治疗后表现出与赤褐袋鼠相似的反应。帚尾袋鼩和肥尾袋鼩对注射的卡麦角林的敏感性低于两种袋鼠科物种,并且帚尾袋鼩对口服给药没有反应。这些有袋动物物种对口服卡麦角林治疗无反应表明,意外摄入用于控制引入的真兽类害虫(如赤狐或野猫)的含20微克/千克卡麦角林的诱饵,不应影响本地有袋动物的繁殖。