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使用神经生长因子/白细胞介素-6比值作为可靠标准,以显示实验性弥漫性脑损伤后孕酮的有益作用。

Using the NGF/IL-6 ratio as a reliable criterion to show the beneficial effects of progesterone after experimental diffuse brain injury.

作者信息

Sara Shirazpour, Mohammad Khaksari, Nader Shahrokhi, Maryam Iranpour, Marzieh Shahryari, Elham Jafari, Neda Salmani

机构信息

Neuroscience Research Center, Neuropharmacology Institute, Kerman University of Medical Sciences, Kerman, Iran.

Endocrinology and Metabolism Research Center, Institute of Basic and Clinical Physiology Sciences, Kerman University of Medical Sciences, Kerman, Iran.

出版信息

Heliyon. 2020 Apr 27;6(4):e03844. doi: 10.1016/j.heliyon.2020.e03844. eCollection 2020 Apr.

DOI:10.1016/j.heliyon.2020.e03844
PMID:32373743
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7191606/
Abstract

Acute progesterone injection has been shown to reduce brain edema following traumatic brain injury (TBI) due to its neuroprotective effect. We investigated the effects of sustained release of progesterone through implantation of subcutaneous capsules on rat's brain edema and alteration of cerebrospinal fluid (CSF), and serum ratio of NGF/IL-6 after TBI. This experiment was performed on ovariectomized (OVX) rats and the brain injury was induced by Marmarou's method. A high and a low dose of progesterone (HP and LP) was injected intraperitoneally two h after the brain injury. In addition, in the capsule progesterone-treated group (CP), the intervention was implemented 6 h after the brain injury. Brain edema, NGF and IL-6 biomarkers in serum and cerebrospinal fluid (CSF) were measured 48 h after the TBI in injection groups and one week after the TBI in the CP group. No significant difference was found in the two groups or in the admonition methods. After TBI, the NGF level increased and IL-6 level decreased by injection of both doses, as well as by taking the capsule. Ratio of NGF/IL-6 in CSF increased significantly by all forms of progesterone administration. The increase in the level of NGF and IL-6 after TBI was higher in CSF than in serum. These results indicated that effects of progesterone in capsule form were better than the injection form. Progesterone probably works by increasing NGF and reducing IL-6. Future studies should investigate the ratio of these biomarkers as a variable to determine the neuroprotective effects of another drug.

摘要

急性注射孕酮已被证明因其神经保护作用可减轻创伤性脑损伤(TBI)后的脑水肿。我们通过植入皮下胶囊持续释放孕酮,研究其对大鼠TBI后脑水肿以及脑脊液(CSF)变化和血清中神经生长因子(NGF)/白细胞介素-6(IL-6)比值的影响。本实验在去卵巢(OVX)大鼠身上进行,脑损伤采用 Marmarou 法诱导。脑损伤后2小时腹腔注射高剂量和低剂量孕酮(HP和LP)。此外,在胶囊孕酮治疗组(CP)中,干预在脑损伤后6小时实施。在注射组TBI后48小时以及CP组TBI后一周测量血清和脑脊液(CSF)中的脑水肿、NGF和IL-6生物标志物。两组或给药方法之间未发现显著差异。TBI后,注射两种剂量孕酮以及服用胶囊均使NGF水平升高,IL-6水平降低。所有形式的孕酮给药均使CSF中NGF/IL-6比值显著升高。TBI后CSF中NGF和IL-6水平的升高高于血清。这些结果表明胶囊形式的孕酮效果优于注射形式。孕酮可能通过增加NGF和降低IL-6发挥作用。未来研究应将这些生物标志物的比值作为一个变量来研究,以确定另一种药物的神经保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/019d703be3ec/gr11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/36af2dca529a/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/ad6ef40863e9/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/a2bbc3c3edee/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/c101ca4ea798/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/5b50cbb848a3/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/d4431eae8919/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/7297e85473eb/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/c6ba7bb3562a/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/95564a94773c/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/5e39db307661/gr10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/019d703be3ec/gr11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/36af2dca529a/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/ad6ef40863e9/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/a2bbc3c3edee/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/c101ca4ea798/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/5b50cbb848a3/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/d4431eae8919/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/7297e85473eb/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/c6ba7bb3562a/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/95564a94773c/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/5e39db307661/gr10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6934/7191606/019d703be3ec/gr11.jpg

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