Naert G, Ixart G, Tapia-Arancibia L, Givalois L
Molecular Mechanisms in Neurodegenerative Dementia Laboratory, Inserm U710, EPHE, University of Montpellier 2, Place Eugène Bataillon, 34095 Montpellier, France.
Neuroscience. 2006 May 12;139(2):779-89. doi: 10.1016/j.neuroscience.2005.12.028. Epub 2006 Feb 2.
Brain-derived neurotrophic factor is a neurotrophin belonging to the nerve growth factor family, which is involved in the differentiation and survival of many types of neurons. It also participates in neuroprotection and neuronal plasticity in adult rats. Our previous studies showed that a single brain-derived neurotrophic factor injection modifies hypothalamic-pituitary-adrenal axis activity in adult male rats. To investigate the effect of chronic brain-derived neurotrophic factor administration on some physiological parameters, adult rats were implanted with osmotic micro-pumps to deliver brain-derived neurotrophic factor continuously for 14 days in the lateral ventricle (12 microg/day/rat). mRNA levels were evaluated by in situ hybridization analysis, peptide contents and plasma hormone concentrations by radioimmunoassay. Animals were also equipped with telemetric transmitters to study locomotor activity and temperature rhythms modifications, since hypothalamic-pituitary-adrenal axis is known to modulate these two parameters. Decreased body weight was used as a control of brain-derived neurotrophic factor access to hypothalamic areas as already documented. In the hypothalamus the continuous brain-derived neurotrophic factor treatment increases: (i) the mRNA steady state levels of corticotropin releasing hormone and arginin-vasopressin in the paraventricular nucleus, the supraoptic nucleus, and the suprachiasmatic nucleus; (ii) the surface of corticotropin releasing hormone and arginin-vasopressin mRNA signals in these nuclei as detected by in situ hybridization, and (iii) the corticotropin releasing hormone and arginin-vasopressin contents. The plasma concentrations of adrenocorticotropic hormone and corticosterone were decreased and increased, respectively. Finally, this treatment increased daily locomotor activity and temperature, and provoked some circadian perturbations. These results obtained after chronic brain-derived neurotrophic factor administration extend data on the brain-derived neurotrophic factor involvement in the hypothalamic-pituitary-adrenal axis regulation and illustrate its effects on the locomotor and temperature rhythms. They also allow demonstrating that the regulation of the hypothalamic-pituitary-adrenal axis by brain-derived neurotrophic factor differs according to the brain-derived neurotrophic factor administration mode, i.e. acute injection or chronic administration.
脑源性神经营养因子是一种属于神经生长因子家族的神经营养蛋白,它参与多种类型神经元的分化和存活。它还参与成年大鼠的神经保护和神经元可塑性。我们之前的研究表明,单次注射脑源性神经营养因子可改变成年雄性大鼠下丘脑 - 垂体 - 肾上腺轴的活性。为了研究长期给予脑源性神经营养因子对一些生理参数的影响,成年大鼠被植入渗透微型泵,以便在侧脑室连续14天给予脑源性神经营养因子(12微克/天/只大鼠)。通过原位杂交分析评估mRNA水平,通过放射免疫测定评估肽含量和血浆激素浓度。动物还配备了遥测发射器,以研究运动活动和体温节律的变化,因为已知下丘脑 - 垂体 - 肾上腺轴可调节这两个参数。体重减轻被用作脑源性神经营养因子进入下丘脑区域的对照,这已得到记录。在下丘脑中,持续给予脑源性神经营养因子会增加:(i)室旁核、视上核和视交叉上核中促肾上腺皮质激素释放激素和精氨酸加压素的mRNA稳态水平;(ii)通过原位杂交检测到的这些核中促肾上腺皮质激素释放激素和精氨酸加压素mRNA信号的面积,以及(iii)促肾上腺皮质激素释放激素和精氨酸加压素的含量。促肾上腺皮质激素和皮质酮的血浆浓度分别降低和升高。最后,这种治疗增加了每日运动活动和体温,并引发了一些昼夜节律紊乱。长期给予脑源性神经营养因子后获得的这些结果扩展了关于脑源性神经营养因子参与下丘脑 - 垂体 - 肾上腺轴调节的数据,并说明了其对运动和体温节律的影响。它们还表明,脑源性神经营养因子对下丘脑 - 垂体 - 肾上腺轴的调节根据脑源性神经营养因子的给药方式而不同,即急性注射或长期给药。