Miller S M, Lonstein J S
Department of Psychology, Michigan State University, East Lansing, MI 48824, USA.
Neuroscience. 2009 Apr 10;159(4):1384-96. doi: 10.1016/j.neuroscience.2009.01.060. Epub 2009 Feb 3.
Dopamine receptor activity in the rodent medial preoptic area (mPOA) is crucial for the display of maternal behaviors, as well as numerous other physiological and behavioral functions. However, the origin of dopaminergic input to the mPOA has not been identified through neuroanatomical tracing. To accomplish this, the retrograde tracer Fluorogold was iontophoretically applied to the mPOA of postpartum laboratory rats, and dual-label immunocytochemistry for Fluorogold and tyrosine hydroxylase later performed to identify dopaminergic cells of the forebrain and midbrain projecting to the mPOA. Results indicate that the number of dopaminergic cells projecting to the mPOA is moderate ( approximately 90 cells to one hemisphere), and that these cells have an unexpectedly wide distribution. Even so, more than half of the dual-labeled cells were found in either what has been considered extensions of the A10 dopamine group (particularly the ventrocaudal posterior hypothalamus and adjacent medial supramammillary nucleus), or in the A10 group of the ventral tegmental area. The rostral hypothalamus and surrounding region also contained numerous dual-labeled cells, with the greatest number found within the mPOA itself (including in the anteroventral preoptic area and preoptic periventricular nucleus). Notably, dual-labeled cells were rare in the zona incerta (A13), a site previously suggested to provide dopaminergic input to the mPOA. This study is the first to use anatomical tracing to detail the dopaminergic projections to the mPOA in the laboratory rat, and indicates that much of this projection originates more caudally than previously suggested.
啮齿动物内侧视前区(mPOA)中的多巴胺受体活性对于母性行为以及许多其他生理和行为功能的表现至关重要。然而,尚未通过神经解剖学追踪确定输入到mPOA的多巴胺能神经支配的起源。为了实现这一点,将逆行示踪剂荧光金离子导入产后实验大鼠的mPOA,随后进行荧光金和酪氨酸羟化酶的双标记免疫细胞化学,以识别投射到mPOA的前脑和中脑的多巴胺能细胞。结果表明,投射到mPOA的多巴胺能细胞数量适中(每个半球约90个细胞),并且这些细胞分布出人意料地广泛。即便如此,超过一半的双标记细胞位于被认为是A10多巴胺组延伸的区域(特别是下丘脑腹尾后区和相邻的内侧乳头体上核),或者位于腹侧被盖区的A10组中。下丘脑前部和周围区域也含有大量双标记细胞,其中数量最多的位于mPOA本身(包括前腹侧视前区和视前室周核)。值得注意的是,在未定带(A13)中双标记细胞很少,该区域先前被认为是向mPOA提供多巴胺能输入的部位。这项研究首次使用解剖学追踪详细描述了实验大鼠中投射到mPOA的多巴胺能神经投射,并表明该投射的大部分起源部位比先前认为的更靠尾侧。