Department of Psychology and Neuroscience, Temple University, Philadelphia, PA, 19122, USA.
Neuroscience Institute and Center for Behavioral Neuroscience, Georgia State University, Atlanta, GA, USA.
Neurochem Int. 2024 Jun;176:105739. doi: 10.1016/j.neuint.2024.105739. Epub 2024 Apr 10.
Corticoptropin releasing factor (CRF) is implicated in stress-related physiological and behavioral changes. The septohippocampal pathway regulates hippocampal-dependent mnemonic processes, which are affected in stress-related disorders, and given the abundance of CRF receptors in the medial septum (MS), this pathway is influenced by CRF. Moreover, there are sex differences in the MS sensitivity to CRF and its impact on hippocampal function. However, the mechanisms underlying these associations remain elusive. In the present study, we utilized an in vivo biosensor-based electrochemistry approach to examine the impact of MS CRF infusions on hippocampal cholinergic signaling dynamics in male and female rats. Our results show increased amplitudes of depolarization-evoked phasic cholinergic signals in the hippocampus following MS infusion of CRF at the 3 ng dose as compared to the infusion involving artificial cerebrospinal fluid (aCSF). Moreover, a trend for a sex × infusion interaction indicated larger cholinergic transients in females. On the contrary, intraseptal infusion of a physiologically high dose (100 ng) of CRF produced a subsequent reduction in phasic cholinergic transients in both males and females. The assessment of tonic cholinergic activity over 30 min post-infusion revealed no changes at the 3 ng CRF dose in either sex, but a significant infusion × sex interaction indicated a reduction in females at the 100 ng dose of CRF as compared to the aCSF. Taken together, our results show differential, dose-dependent modulatory effects of MS CRF on the dynamics of phasic and tonic modes of cholinergic signaling in the hippocampus of male and female rats. These cholinergic signaling modes are critical for memory encoding and maintaining arousal states, and may underlie sex differences in cognitive vulnerability to stress and stress-related psychiatric disorders.
促肾上腺皮质激素释放因子(CRF)与应激相关的生理和行为变化有关。隔海马通路调节海马依赖性记忆过程,这些过程在应激相关障碍中受到影响,并且由于 CRF 受体在中隔(MS)中丰富,因此该通路受 CRF 影响。此外,MS 对 CRF 的敏感性及其对海马功能的影响存在性别差异。然而,这些关联的潜在机制仍然难以捉摸。在本研究中,我们利用基于活体生物传感器的电化学方法,研究了 MS CRF 输注对雄性和雌性大鼠海马胆碱能信号动力学的影响。我们的结果表明,与涉及人工脑脊液(aCSF)的输注相比,MS 中 CRF 输注在 3ng 剂量下会增加海马中去极化诱发的胆碱能信号的幅度。此外,性别×输注相互作用的趋势表明女性的胆碱能瞬变更大。相反,在中隔内输注生理上较高剂量(100ng)的 CRF 会导致雄性和雌性的胆碱能瞬变随后减少。在输注后 30 分钟内评估紧张性胆碱能活性,在两性中,3ng CRF 剂量均未发生变化,但输注×性别相互作用表明,与 aCSF 相比,在 100ng CRF 剂量下,女性的胆碱能活性降低。总之,我们的结果表明,MS CRF 对雄性和雌性大鼠海马中胆碱能信号的瞬变和紧张模式的动态具有不同的、剂量依赖性的调节作用。这些胆碱能信号模式对于记忆编码和维持觉醒状态至关重要,并且可能是认知对压力和应激相关精神障碍易感性的性别差异的基础。