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Ten-神经素C末端关联肽(TCAP)-1减轻雄性小鼠和大鼠的束缚应激诱导的皮质酮升高。

Teneurin C-Terminal Associated Peptide (TCAP)-1 Attenuates Restraint Stress-Induced Corticosterone Increases in Male Mice and Rats.

作者信息

Mueller Lauren E, Wexler Roseanne S, Lovejoy David A, Stein Robert B, Slee Andrew M

机构信息

Protagenic Therapeutics Inc., New York, New York, USA.

NeoSome Life Science, Lexington, Massachusetts, USA.

出版信息

Pharmacol Res Perspect. 2024 Dec;12(6):e70045. doi: 10.1002/prp2.70045.

DOI:10.1002/prp2.70045
PMID:39651597
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11626411/
Abstract

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.

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,因此需要有效的治疗方法来减轻这种适应不良的反应。在此,我们研究了Tenascin C末端相关肽(TCAP)-1对压力生理表现的影响,已知该肽可抑制促肾上腺皮质激素释放因子(CRF)介导的应激反应,以及TCAP-1的作用是否依赖于给药途径。我们首先研究了皮下注射TCAP-1是否会影响雄性小鼠和大鼠因束缚应激诱导的皮质酮(CORT)升高。使用类似模型,我们进一步研究了鼻内给予TCAP-1的疗效和时间进程。结果表明,皮下注射TCAP-1可减轻雄性小鼠和大鼠应激生理表现的表达,预防性给予鼻内TCAP-1可有效减轻雄性大鼠应激诱导的CORT升高。这些数据表明,通过非侵入性给药途径给予TCAP-1可能具有作为临床相关抗焦虑药物的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe1f/11626411/dac30a2200dd/PRP2-12-e70045-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe1f/11626411/d2acf2124326/PRP2-12-e70045-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe1f/11626411/c954839c0b4a/PRP2-12-e70045-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe1f/11626411/67c89b1d3168/PRP2-12-e70045-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe1f/11626411/dac30a2200dd/PRP2-12-e70045-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe1f/11626411/d2acf2124326/PRP2-12-e70045-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe1f/11626411/c954839c0b4a/PRP2-12-e70045-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe1f/11626411/67c89b1d3168/PRP2-12-e70045-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe1f/11626411/dac30a2200dd/PRP2-12-e70045-g003.jpg

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本文引用的文献

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Psychopharmacology (Berl). 2024 Aug;241(8):1565-1575. doi: 10.1007/s00213-024-06582-0. Epub 2024 Apr 17.
2
Evaluation of Recent Intranasal Drug Delivery Systems to the Central Nervous System.近期中枢神经系统鼻内给药系统的评估
Pharmaceutics. 2022 Mar 12;14(3):629. doi: 10.3390/pharmaceutics14030629.
3
Intranasal drug delivery: opportunities and toxicologic challenges during drug development.
鼻腔内给药:药物开发过程中的机遇和毒理学挑战。
Drug Deliv Transl Res. 2022 Apr;12(4):735-757. doi: 10.1007/s13346-020-00891-5. Epub 2021 Jan 25.
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Pharmacological Treatment of Anxiety Disorders: The Role of the HPA Axis.焦虑症的药物治疗:下丘脑-垂体-肾上腺轴的作用
Front Psychiatry. 2020 May 15;11:443. doi: 10.3389/fpsyt.2020.00443. eCollection 2020.
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Differential effects of stress exposure via two types of restraint apparatuses on behavior and plasma corticosterone level in inbred male BALB/cAJcl mice.两种束缚装置致同种系雄性 BALB/cAJcl 小鼠应激暴露的行为学及血浆皮质酮水平的差异效应。
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Mechanism of intranasal drug delivery directly to the brain.鼻内给药直接作用于大脑的机制。
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