2019
DOI: 10.3892/etm.2019.8029
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Exogenous brain‑derived neurotrophic factor attenuates neuronal apoptosis and neurological deficits after subarachnoid hemorrhage in rats

Abstract: Brain-derived neurotrophic factor (BDNF) is a growth factor crucial for neuronal survival, while its role in subarachnoid hemorrhage (SAH)-induced neuronal apoptosis remains unclear. The aim of the present study was to investigate whether administering exogenous BDNF can protect against neuronal apoptosis and neurological deficits following SAH in a rat model. The BDNF level was found to be significantly decreased in the basal cortex at 6, 12, 24, 48 and 72 h following SAH. Exogenous BDNF significantly decreas… Show more

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Cited by 9 publications
(5 citation statements)
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References 30 publications
(48 reference statements)
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“…Furthermore, there are studies that link lower levels of BDNF with neonatal periventricular hemorrhage secondary to hypoxic-ischemic lesions [26]. Likewise, as a therapeutic approach, BDNF is being studied for neuroprotection, reducing cell apoptosis in the face of external insults, promoting specific populations of neurons in both central and peripheral nervous systems as well as after hypoxic or inflammatory brain injuries [27][28][29]. On the other hand, since the origin of neonatal BDNF in cord blood is believed to be a reflection of brain levels in animal studies [30], there are publications in the medical literature that assess BDNF levels as a predictor of behavior diseases [31] and its role in major depression, autism spectrum disorders and degenerative diseases [32,33].…”
Section: Introductionmentioning
confidence: 99%
“…Furthermore, there are studies that link lower levels of BDNF with neonatal periventricular hemorrhage secondary to hypoxic-ischemic lesions [26]. Likewise, as a therapeutic approach, BDNF is being studied for neuroprotection, reducing cell apoptosis in the face of external insults, promoting specific populations of neurons in both central and peripheral nervous systems as well as after hypoxic or inflammatory brain injuries [27][28][29]. On the other hand, since the origin of neonatal BDNF in cord blood is believed to be a reflection of brain levels in animal studies [30], there are publications in the medical literature that assess BDNF levels as a predictor of behavior diseases [31] and its role in major depression, autism spectrum disorders and degenerative diseases [32,33].…”
Section: Introductionmentioning
confidence: 99%
“…BDNF plays central roles in synaptic plasticity and neuronal development, and animal models suggest that exogenous BDNF has neuroprotective effects, improving neurological deficits in different brain injuries, including TBI, hypoxicischemic brain injury, and subarachnoid hemorrhage [52][53][54]. Efforts to enhance BDNF expression with rehabilitative strategies are still in the early stage, and this study showed that verticalization with robot-assisted lower-limb training is inadequate for the promotion of BDNF-mediated plastic changes in patients with DOCs.…”
Section: Discussionmentioning
confidence: 82%
“…The higher bdnf expression in the CPF-exposed groups reflects its effect on scavenging the toxic effects of CPF. Indeed, bdnf is known as a promoter of dendritic genesis, ensuring nerve cell survival, it plays key roles in growth, differentiation, and synaptic plasticity [ 71 , 72 ], and it reduces neuronal apoptosis [ 73 ]. Bdnf immunolabeling in curative and preventive groups was slightly lower than that of the CPF group ( p ˂ 0.05).…”
Section: Discussionmentioning
confidence: 99%