Lauren E Mueller, Roseanne S Wexler, David A Lovejoy, Robert B Stein, Andrew M Slee
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引用次数: 0
摘要
下丘脑-垂体-肾上腺(HPA)轴反应的过度激活可导致焦虑和其他神经精神疾病,需要有效的治疗来减轻这种适应不良反应。在这里,我们研究了Teneurin c -末端相关肽(TCAP)-1对应激生理表达的影响,以及TCAP-1的作用是否依赖于给药途径。TCAP-1是一种已知可抑制促肾上腺皮质激素释放因子(CRF)介导的应激的肽。我们首先研究了皮下给药TCAP-1是否会影响雄性小鼠和大鼠的管约束应激性皮质酮(CORT)的增加。使用类似的模型,我们进一步研究了鼻内TCAP-1的疗效和时间过程。结果表明,皮下给药TCAP-1可减弱雄性小鼠和大鼠应激生理表现的表达,而预防性鼻内给药TCAP-1可有效减弱应激诱导的雄性大鼠CORT升高。这些数据表明,通过非侵入性给药途径给药的TCAP-1可能具有作为临床相关抗焦虑药的潜力。
Teneurin C-Terminal Associated Peptide (TCAP)-1 Attenuates Restraint Stress-Induced Corticosterone Increases in Male Mice and Rats.
Hyperactivation of the hypothalamic-pituitary-adrenal (HPA) axis response can result in anxiety and other neuropsychiatric disorders and effective therapeutics are needed to mitigate this maladaptive response. Here we examined the effects of Teneurin C-terminal Associated Peptide (TCAP)-1, a peptide known to inhibit corticotropin releasing factor (CRF)-mediated stress, on the physiological expression of stress, and whether the effects of TCAP-1 were dependent on the route of administration. We first examined whether subcutaneous administration of TCAP-1 influenced tube restraint stress-induced corticosterone (CORT) increases in both male mice and rats. Using a similar model, we further examined the efficacy and time course of intranasal TCAP-1. Results showed that subcutaneous TCAP-1 administration attenuated the expression of the physiological manifestation of stress in male mice and rats, and that intranasal TCAP-1 delivered prophylactically is effective at attenuating stress-induced CORT increases in male rats. These data indicate that TCAP-1 delivered though non-invasive routes of administration could have potential as a clinically relevant anxiolytic.
期刊介绍:
PR&P is jointly published by the American Society for Pharmacology and Experimental Therapeutics (ASPET), the British Pharmacological Society (BPS), and Wiley. PR&P is a bi-monthly open access journal that publishes a range of article types, including: target validation (preclinical papers that show a hypothesis is incorrect or papers on drugs that have failed in early clinical development); drug discovery reviews (strategy, hypotheses, and data resulting in a successful therapeutic drug); frontiers in translational medicine (drug and target validation for an unmet therapeutic need); pharmacological hypotheses (reviews that are oriented to inform a novel hypothesis); and replication studies (work that refutes key findings [failed replication] and work that validates key findings). PR&P publishes papers submitted directly to the journal and those referred from the journals of ASPET and the BPS