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在催产素基因敲除的雄性和雌性小鼠中,血管加压素通过催产素受体刺激下丘脑腹内侧神经元。

Vasopressin stimulates ventromedial hypothalamic neurons via oxytocin receptors in oxytocin gene knockout male and female mice.

作者信息

Ragnauth André K, Goodwillie Andrew, Brewer Cornelia, Muglia Louis J, Pfaff Donald W, Kow Lee-Ming

机构信息

Laboratory of Neurobiology and Behavior, The Rockefeller University, New York, NY 10021, USA.

出版信息

Neuroendocrinology. 2004;80(2):92-9. doi: 10.1159/000081844. Epub 2004 Nov 2.

DOI:10.1159/000081844
PMID:15528951
Abstract

A wealth of neuropharmacological data demonstrates that oxytocin (OT) actions in the mammalian forebrain support a wide variety of affiliative behaviors and repress aggressive behaviors. Based on that literature, it was expected that reproductive and affiliative behaviors would be vastly decreased and aggression markedly increased in OT gene knockout (OTKO) mice. The initial publications reporting the behaviors of these mice did not include such phenotypes. Here, we compared single-unit activities recorded from the ventromedial hypothalamus in tissue slices of male and female OTKO mice and their wild-type littermate to test two hypotheses about OT functional genomics. First, we proposed that in OTKO mice, a very similar 9-amino-acid neuropeptide, arginine vasopressin (a likely gene duplication product), can 'cross over' and compensate for the lack of OT. This hypothesis was confirmed in both males and females. Further, we proposed that because of the lifelong absence of OT in OTKO, OT receptors would be more sensitive to OT in the knockout animals. We tested this idea in males and found that it was correct. Thus, an answer to the 'OTKO paradox' is put forth, with implications for OT-sensitive behaviors in a variety of species.

摘要

大量神经药理学数据表明,催产素(OT)在哺乳动物前脑的作用支持多种亲和行为并抑制攻击行为。基于该文献,预计OT基因敲除(OTKO)小鼠的生殖和亲和行为会大幅减少,攻击行为会显著增加。最初报道这些小鼠行为的出版物并未包括此类表型。在此,我们比较了雄性和雌性OTKO小鼠及其野生型同窝仔鼠组织切片中腹内侧下丘脑记录的单单位活动,以检验关于OT功能基因组学的两个假设。首先,我们提出在OTKO小鼠中,一种非常相似的9氨基酸神经肽,精氨酸加压素(可能是基因复制产物)可以“交叉”并弥补OT的缺乏。这一假设在雄性和雌性小鼠中均得到证实。此外,我们提出由于OTKO小鼠终生缺乏OT,OT受体在基因敲除动物中对OT会更敏感。我们在雄性小鼠中测试了这一想法,发现它是正确的。因此,我们提出了对“OTKO悖论”的一个答案,这对多种物种中OT敏感行为具有启示意义。

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1
Vasopressin stimulates ventromedial hypothalamic neurons via oxytocin receptors in oxytocin gene knockout male and female mice.在催产素基因敲除的雄性和雌性小鼠中,血管加压素通过催产素受体刺激下丘脑腹内侧神经元。
Neuroendocrinology. 2004;80(2):92-9. doi: 10.1159/000081844. Epub 2004 Nov 2.
2
Female oxytocin gene-knockout mice, in a semi-natural environment, display exaggerated aggressive behavior.在半自然环境中,雌性催产素基因敲除小鼠表现出过度的攻击行为。
Genes Brain Behav. 2005 Jun;4(4):229-39. doi: 10.1111/j.1601-183X.2005.00118.x.
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Hippocampal gene expression patterns in oxytocin male knockout mice are related to impaired social interaction.催产素缺乏雄性小鼠海马基因表达模式与社交障碍有关。
Behav Brain Res. 2019 May 17;364:464-468. doi: 10.1016/j.bbr.2017.10.034. Epub 2017 Nov 2.
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Maternal separation interferes with developmental changes in brain vasopressin and oxytocin receptor binding in male rats.母婴分离会干扰雄性大鼠脑血管加压素和催产素受体结合的发育变化。
Neuropharmacology. 2010 Jan;58(1):78-87. doi: 10.1016/j.neuropharm.2009.06.020. Epub 2009 Jun 26.
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Mutual regulation of vasopressin- and oxytocin-induced glucagon secretion in V1b vasopressin receptor knockout mice.血管升压素1b受体基因敲除小鼠中血管升压素和催产素诱导的胰高血糖素分泌的相互调节
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The Impact of Oxytocin Gene Knockout on Sexual Behavior and Gene Expression Related to Neuroendocrine Systems in the Brain of Female Mice.催产素基因敲除对雌性小鼠大脑性行为及与神经内分泌系统相关基因表达的影响。
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Oxytocin modulates social interaction but is not essential for sexual behavior in male mice.催产素调节社会互动,但不是雄性小鼠性行为所必需的。
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Distribution of vasopressin and oxytocin binding sites in the brain and upper spinal cord of the common marmoset.普通狨猴大脑和上脊髓中血管加压素和催产素结合位点的分布。
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Effects of a single administration of oxytocin or vasopressin and their interactions with two selective receptor antagonists on memory storage in mice.单次注射催产素或加压素及其与两种选择性受体拮抗剂的相互作用对小鼠记忆存储的影响。
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Vasopressin and oxytocin receptor systems in the brain: Sex differences and sex-specific regulation of social behavior.大脑中的血管加压素和催产素受体系统:性别差异与社会行为的性别特异性调节
Front Neuroendocrinol. 2016 Jan;40:1-23. doi: 10.1016/j.yfrne.2015.04.003. Epub 2015 May 4.

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