Bosch Oliver J, Neumann Inga D
Department of Behavioural Neuroendocrinology, Institute of Zoology, University of Regensburg, 93040 Regensburg, Germany.
Proc Natl Acad Sci U S A. 2008 Nov 4;105(44):17139-44. doi: 10.1073/pnas.0807412105. Epub 2008 Oct 27.
The neuropeptide arginine vasopressin (AVP) is arguably among the most potent regulators of social behaviors in mammals identified to date. However, only the related neuropeptide oxytocin (OXT) has been shown to promote maternal behavior. Here, we assess the role of AVP in maternal care, in particular in arched back nursing, pup retrieval, and pup contact by using complementary pharmacological and genetic approaches. Also, experiments were performed in rat dams with differences in trait anxiety, i.e., rats bred for either high (HAB) or low (LAB) anxiety-related behavior as well as nonselected (NAB) dams. Viral vector-mediated up-regulation of AVP V1a receptors (AVP-Rs) within the medial preoptic area of lactating NAB rats and chronic central AVP treatment of NAB and LAB dams improved, whereas local blockade of AVP-R expression by means of antisense oligodeoxynucleotides or central AVP-R antagonism impaired, maternal care in NAB dams. Also, in HAB rats with a genetically determined elevated brain AVP activity, intrinsically high levels of maternal care were reversed by blockade of AVP-R actions. Treatment-induced impairment of AVP-mediated maternal behavior increased adult emotionality and impaired social interactions in male offspring of NAB dams. These findings provide direct evidence for an essential and highly potent role of brain AVP in promoting maternal behavior, which seems to be independent of the dam's trait anxiety.
神经肽精氨酸加压素(AVP)可以说是迄今为止已确定的哺乳动物社会行为最有效的调节因子之一。然而,只有相关神经肽催产素(OXT)已被证明能促进母性行为。在这里,我们通过使用互补的药理学和遗传学方法,评估AVP在母性关怀中的作用,特别是在弓背哺乳、幼崽找回和幼崽接触方面的作用。此外,还对具有不同特质焦虑的大鼠母鼠进行了实验,即繁殖出的具有高(HAB)或低(LAB)焦虑相关行为的大鼠以及未选择(NAB)的母鼠。病毒载体介导的哺乳期NAB大鼠视前内侧区AVP V1a受体(AVP-Rs)上调以及对NAB和LAB母鼠进行慢性中枢AVP治疗可改善母性关怀,而通过反义寡脱氧核苷酸局部阻断AVP-R表达或中枢AVP-R拮抗作用则会损害NAB母鼠的母性关怀。此外,在具有遗传决定的脑AVP活性升高的HAB大鼠中,通过阻断AVP-R作用可逆转原本高水平的母性关怀。治疗诱导的AVP介导的母性行为损伤增加了成年雄性后代的情绪反应,并损害了其社交互动。这些发现为脑AVP在促进母性行为中发挥重要且高效的作用提供了直接证据,这一作用似乎与母鼠的特质焦虑无关。