Sex differences in mouse infralimbic cortex projections to the nucleus accumbens shell

IF 4.9 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Caroline S. Johnson, Andrew D. Chapp, Erin B. Lind, Mark J. Thomas, Paul G. Mermelstein
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Abstract

The nucleus accumbens (NAc) is an important region in motivation and reward. Glutamatergic inputs from the infralimbic cortex (ILC) to the shell region of the NAc (NAcSh) have been implicated in driving the motivation to seek reward through repeated action-based behavior. While this has primarily been studied in males, observed sex differences in motivational circuitry and behavior suggest that females may be more sensitive to rewarding stimuli. These differences have been implicated for the observed vulnerability in women to substance use disorders. We used an optogenetic self-stimulation task in addition to ex vivo electrophysiological recordings of NAcSh neurons in mouse brain slices to investigate potential sex differences in ILC-NAcSh circuitry in reward-seeking behavior. Glutamatergic neurons in the ILC were infected with an AAV delivering DNA encoding for channelrhodopsin. Entering the designated active corner of an open field arena resulted in photostimulation of the ILC terminals in the NAcSh. Self-stimulation occurred during two consecutive days of testing over three consecutive weeks: first for 10 Hz, then 20 Hz, then 30 Hz. Whole-cell recordings of medium spiny neurons in the NAcSh assessed both optogenetically evoked local field potentials and intrinsic excitability. Although both sexes learned to seek the active zone, within the first day, females entered the zone more than males, resulting in a greater amount of photostimulation. Increasing the frequency of optogenetic stimulation amplified female reward-seeking behavior. Males were less sensitive to ILC stimulation, with higher frequencies and repeated days required to increase male reward-seeking behavior. Unexpectedly, ex vivo optogenetic local field potentials in the NAcSh were greater in slices from male animals. In contrast, female medium-spiny neurons (MSNs) displayed significantly greater intrinsic neuronal excitability. Taken together, these data indicate that there are sex differences in the motivated behavior driven by glutamate within the ILC-NAcSh circuit. Though glutamatergic signaling was greater in males, heightened intrinsic excitability in females appears to drive this sex difference. The shell region of the nucleus accumbens (NAcSh) is involved in motivation and reward. It receives excitatory glutamatergic inputs from multiple brain regions. One specific region is the infralimbic cortex (ILC), which when activated, influences reward-seeking behavior. While previous research has focused on males, there are inherent sex differences in reward circuitry and reward-seeking behavior. Using an optogenetic self-stimulation task, in addition to ex vivo electrophysiological recordings, we found inherent sex differences in the ILC-NAcSh circuit in behavioral output, synaptic strength, and intrinsic neurophysiology. Female mice showed more robust reward-seeking behavior. Increasing the frequency of stimulation intensified this behavior in females, while males required higher frequencies and repeated testing days to increase their reward-seeking behavior. Surprisingly, optogenetically stimulating the ILC terminals in the NAcSh in brain slices resulted in stronger responses in males. More consistent with the behavioral data, female MSNs displayed higher intrinsic excitability. Our results suggest that there are sex differences in motivated behavior, driven by glutamatergic signaling in the ILC-NAc circuit. Despite stronger ILC-based glutamatergic signaling in males, heightened intrinsic excitability of MSNs in females seems to be the driving force behind this sex difference in reward-seeking behavior. These findings contribute to our understanding of the neural mechanisms behind sex-based differences in motivation and their potential implications for substance use disorders.
小鼠下边缘皮层投射到伏隔核外壳的性别差异
纳氏核(Narc)是动机和奖赏的重要区域。从下边缘皮层(ILC)到 NAc 壳区(NAcSh)的谷氨酸能输入被认为与通过重复动作行为寻求奖赏的动机有关。虽然这项研究主要针对男性,但观察到的动机回路和行为的性别差异表明,女性可能对奖赏刺激更加敏感。这些差异被认为是女性易患药物使用障碍的原因。除了对小鼠脑片中的NAcSh神经元进行体外电生理记录外,我们还使用了光遗传自刺激任务来研究ILC-NAcSh回路在奖赏寻求行为中的潜在性别差异。ILC中的谷氨酸能神经元感染了一种AAV,该AAV可提供编码channelrhodopsin的DNA。在连续三周进行的连续两天的测试中都会出现自我刺激:首先是10赫兹,然后是20赫兹,最后是30赫兹。对NarcSh中刺神经元的全细胞记录评估了光诱发的局部场电位和内在兴奋性。尽管雌雄动物都学会了寻找活跃区,但在第一天内,雌性动物进入活跃区的次数多于雄性动物,从而导致光刺激量增加。增加光遗传刺激的频率会放大雌性寻求奖赏的行为。雄性对ILC刺激的敏感性较低,需要更高的频率和重复的天数才能增加雄性寻求奖赏的行为。意想不到的是,雄性动物的切片在NarcSh中的体外光遗传局部场电位更高。相比之下,雌性中刺神经元(MSN)的内在神经元兴奋性明显更高。综上所述,这些数据表明,ILC-NAcSh回路中谷氨酸驱动的动机行为存在性别差异。虽然谷氨酸能信号在雄性中更强,但雌性中更强的内在兴奋性似乎是这种性别差异的驱动因素。伏隔核的外壳区(NAcSh)与动机和奖赏有关。它接受来自多个脑区的兴奋性谷氨酸能输入。其中一个特定区域是下边缘皮层(ILC),该区域被激活后会影响寻求奖赏的行为。以往的研究主要集中在男性身上,但奖赏回路和奖赏寻求行为存在固有的性别差异。除了体内外电生理记录外,我们还利用光遗传自刺激任务发现了 ILC-NAcSh 电路在行为输出、突触强度和内在神经生理学方面的固有性别差异。雌性小鼠表现出更强烈的奖赏寻求行为。增加刺激频率可强化雌性小鼠的这种行为,而雄性小鼠则需要更高的频率和重复测试天数才能增加其寻求奖赏的行为。令人惊讶的是,通过光遗传刺激脑片中NAcSh的ILC末端,雄性会产生更强烈的反应。与行为数据更加一致的是,雌性MSN显示出更高的内在兴奋性。我们的研究结果表明,在ILC-NAc回路的谷氨酸能信号驱动下,动机行为存在性别差异。尽管男性基于 ILC 的谷氨酸能信号更强,但女性 MSNs 内在兴奋性的提高似乎是这种寻求奖赏行为性别差异背后的驱动力。这些发现有助于我们了解基于性别的动机差异背后的神经机制及其对药物使用障碍的潜在影响。
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来源期刊
Biology of Sex Differences
Biology of Sex Differences ENDOCRINOLOGY & METABOLISM-GENETICS & HEREDITY
CiteScore
12.10
自引率
1.30%
发文量
69
审稿时长
14 weeks
期刊介绍: Biology of Sex Differences is a unique scientific journal focusing on sex differences in physiology, behavior, and disease from molecular to phenotypic levels, incorporating both basic and clinical research. The journal aims to enhance understanding of basic principles and facilitate the development of therapeutic and diagnostic tools specific to sex differences. As an open-access journal, it is the official publication of the Organization for the Study of Sex Differences and co-published by the Society for Women's Health Research. Topical areas include, but are not limited to sex differences in: genomics; the microbiome; epigenetics; molecular and cell biology; tissue biology; physiology; interaction of tissue systems, in any system including adipose, behavioral, cardiovascular, immune, muscular, neural, renal, and skeletal; clinical studies bearing on sex differences in disease or response to therapy.
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