Stolzenberg Danielle S, McKenna Jonathan B, Keough Samantha, Hancock Rebecca, Numan Marilyn J, Numan Michael
Department of Psychology, Boston College, Chestnut Hill, MA 02467, USA.
Behav Neurosci. 2007 Oct;121(5):907-19. doi: 10.1037/0735-7044.121.5.907.
There is good evidence that interference with the mesolimbic dopamine (DA) system results in impaired maternal responding in postpartum female rats. However, whether activation of the mesolimbic DA system is capable of promoting maternal behavior has not been investigated. This study examined whether increasing DA activity in various brain regions of pregnancy-terminated, naive female rats would stimulate the onset of maternal behavior. Experiments 1 and 2 examined the effects of microinjection of various doses (0, 0.2, or 0.5 microg/0.5 microl/side) of a D1 DA receptor agonist, SKF 38393, or a D2 DA receptor agonist, quinpirole, into the nucleus accumbens (NA) on latency to show full maternal behavior, and Experiment 3 determined the effects of SKF 38393 injection into a control site. Finally, because the medial preoptic area (MPOA) is also important for maternal behavior, receives DA input, and expresses DA receptors, the authors examined whether microinjection of SKF 38393 into MPOA was capable of stimulating the onset of maternal behavior. Results indicated that microinjection of SKF 38393 into either the NA or the MPOA facilitates maternal responding in pregnancy-terminated rats.
有充分证据表明,干扰中脑边缘多巴胺(DA)系统会导致产后雌性大鼠的母性行为受损。然而,中脑边缘DA系统的激活是否能够促进母性行为尚未得到研究。本研究考察了在妊娠结束的未育雌性大鼠的不同脑区增加DA活性是否会刺激母性行为的开始。实验1和实验2研究了向伏隔核(NA)微量注射不同剂量(0、0.2或0.5微克/0.5微升/侧)的D1 DA受体激动剂SKF 38393或D2 DA受体激动剂喹吡罗对展现完全母性行为的潜伏期的影响,实验3则确定了向对照部位注射SKF 38393的效果。最后,由于内侧视前区(MPOA)对母性行为也很重要,接受DA输入并表达DA受体,作者考察了向MPOA微量注射SKF 38393是否能够刺激母性行为的开始。结果表明,向NA或MPOA微量注射SKF 38393均可促进妊娠结束大鼠的母性行为反应。