The role of neurotrophins NGF (nerve growth factor) and BDNF (brain derived neurotrophic factor) in the structural integrity of the nervous system makes them attractive candidates as therapeutic agents for a number of neurodegenerative disorders. There is a growing body of evidence indicating the role of NGF and BDNF in recovery after a stroke. The both neurotrophins have been reported to reduce infarct volumes and improve neurological outcomes in animal models of cerebral ischemia [ 1 - 5 ] . The mechanisms of the neuroprotective and neurorestorative capability of NGF and BDNF include antioxidant and anti-apoptotic effects, modulation of local inflammatory processes and promotion of neurogenesis [ 1 , 6 - 11 ]. However, clinical use of neurotrophins is limited because of the difficulties in protein delivery to the central nervous system and undesirable side effects due to pleiotropic functions. The design of small, proteolytically stable compounds that exert defined biological activities via the selective activation of neurotrophins signaling might provide a useful approach for the development of therapeutic agents.
NGF and BDNF exert their main biological actions through TrkA and TrkB receptors respectively. Binding neurotrophin with Trk tyrosine kinase receptors leads to the activation of various intracellular signaling pathways, including the PI3K/AKT and MAPK/ERK, which are the most critical for the biological effects of these regulatory proteins.
The working hypothesis formed by Gudasheva T.A. et al. [ 12 ] goes that by interacting with the same receptor multiple neurotrophin hairpin loops can activate various intracellular signaling cascades and are therefore responsible for an array of neurotrophin effects. Within the framework of this hypothesis, a number of dimeric dipeptide mimetics of NGF and BDNF loops were designed and synthesized in the V.V. Zakusov institute of pharmacology (Ru Patent №2410392, 2010; US Patent US 9683014 B2, 2017; CN Patent CN 102365294 B, 2016) [ 12 , 13 ]. The beta-turn sequences of NGF or BDNF hairpin loops were chosen as the basis of the design because they are most likely to interact with the receptor due to their accessibility.
Here we report a comparative analysis of neuroprotective activity of the three most active in vitro compounds in a model of ischemic stroke, induced by transient middle cerebral artery occlusion (MCAO) in rats. These are the mimetics of BDNF loops 1 and 4, respectively bis-(N-monosuccinyl-L-methionyl-L-serine) heptamethylenediamide (GSB-214) and bis-(N-monosuccinyl-L-seryl-L-lysine) hexamethylenediamide (GSB-106), and the mimetic of NGF loop 4, bis(N-succinyl-Lglutamyl-L-lysine) hexamethylenediamide (GK-2). Previously it was shown by the western blot analysis that all the obtained dipeptides activated a corresponding specific NGF or BDNF tyrosine kinase receptor (TrkA or TrkB) but these dipeptides had different postreceptor signaling patterns [ 14 , 15 ]. GSB-106 increased the levels of ERK and AKT kinase phosphorylation, whereas GSB-214 and GK-2 only increased the level of AKT phosphorylation. Structures and patterns of signaling pathways activation of these NGF and BDNF mimetics are presented in Table 1 and in Figure 1.
Figure 1. Chemical structures of the NGF (GK-2) and BDNF (GSB-106, GSB-214) mimetics.
Table 1. Structures and patterns of signaling pathways activation of dimeric dipeptide NGF and BDNF mimetics.
A rat model of transient middle cerebral artery occlusion was established using the intraluminal suture method [ 16 ]. The study was carried out in accordance with the requirements of Directive 2010/63/EU of the European Parliament and with the Order of the Ministry of Health Care and Social Development of the Russian Federation N˚ 708n of 23.08.2010 “Approval of the Rules of Good Laboratory Practice”. All the experiments were approved by the Institutional Animal Care and Use Committee of Zakusov Institute of Pharmacology (Moscow).
The rats were anesthetized with an ip injection of nembutal (60 mg/kg). The right common carotid artery, internal carotid artery, and external carotid artery were surgically exposed. A nylon suture with a silicon-coated tip was inserted from the external carotid artery into the internal carotid artery and then to the circle of Willis to occlude the origin of the middle cerebral artery. In 1 h after MCAO, the suture was carefully removed to induce reperfusion. The rats receiving MCAO that did not have any neurological deficits when awakening were excluded. The remaining animals were randomly divided into treated and untreated (MCAO) groups with at least six animals in each. GSB-106, GSB-214 or GK-2 (dissolved in distilled water) were administered ip at doses of 0.1, 0.1 and 1 mg/kg respectively, daily 4 h after MCAO for 7 days. These doses were chosen as the most pharmacologically active based on preliminary in vivo studies [ 13 , 17 ]. The MCAO group was treated with distilled water in the same regime. The mimetics of BDNF and NGF mimetic were studied in the two independent experiments in outbred rats. In addition, we studied neuroprotective effects of GK-2 with the treatment beginning 6, 8 and 24 hours after reperfusion. There were three independent experiments in Wistar rats. The cerebral infarct volumes were measured with 2,3,5-triphenyltetrazolium chloride (TTC) staining 21 days after MCAO in the experiment with GSB-106 and GSB-214 and 7 days after MCAO in the experiments with GK-2.
3. RESULTS AND DISCUSSION
All the three dimeric dipeptides showed statistically significant decrease of infarct volumes with the treatment beginning 4 hour after surgery. In the experiment with BDNF mimetics [ 15 ], the median infarct volume in MCAO group was 268 mm3 (Figure 2, Table 2). GSB-106 reduced this volume to 90 mm3 (p = 0.01) and GSB-214 to 194 mm3 (p = 0.02). In the experiment with NGF mimetic the median infarct volume in the MCAO group was 255 mm3. GK-2 reduced the cerebral infarct volume to 141 mm3 by approximately 45% (p = 0.03) (Figure 2, Table 2).
Thus, BDNF mimetic GSB-106, which activated both the PI3K/AKT and MAPK/ERK cascades, and NGF mimetic GK-2, which selectively activated PI3K/AKT, showed high neuroprotective efficacy. BDNF mimetic GSB-214, which selectively activated PI3K/AKT signaling, showed low efficiency.
It is widely known that PI3K/AKT and MAPK/ERK pathways are two major intracellular signaling networks activated by growth factors responsible for the cell survival [ 18 ]. It has been reported that NGF mediated neuroprotective signaling is most likely to depend on PI3K/AKT rather than MAPK/ERK pathway [ 19 - 21 ]. The results obtained in the current study indicate that selective activation of PI3K/AKT by NGF mimetic is sufficient for the manifestation of neuroprotective activity in vivo. The lack of the MAP
Figure 2. Dimeric dipeptide mimetics of NGF and BDNF decrease infarct volume after middle cerebral artery occlusion in outbred rats with the treatment beginning 4 hour after surgery. Scatter dot plots (median with interquartile range) of cerebral infarct volumes (mm3). #-p < 0.05 vs. the MCAO group (Mann-Whitney U-test). *-p < 0.05, * -p = 0.01 vs. the MCAO group (Mann-Whitney U-test with Bonferroni’s correction).
Table 2. Dimeric dipeptide mimetics of NGF and BDNF decrease infarct volume after middle cerebral artery occlusion in outbred rats with the treatment beginning 4 hour after surgery.
Notes: The NGF and BDNF mimetics were studied in the two independent experiments in the model of middle cerebral artery occlusion in rats (respectively experiment 1 and experiment 2). The data are presented as medians and interquartile ranges. #-p < 0.05 vs. the MCAO group (Mann-Whitney U-test). *-p < 0.05, **-p = 0.01 vs. the MCAO group (Mann-Whitney U-test with Bonferroni’s correction).
kinase pathway activation appears to be an advantageous pharmacological property for the NGF mimetic, since there is evidence that this pathway of TrkA receptors is involved in the development of hyperalgesia [ 22 ]. It was established that GK-2 has no side effects accompanying NGF treatment namely hyperalgesia and weight loss whereas the activation of both the PI3K/AKT and MAPK/ERK pathways by NGF loop 1 dimeric dipeptide mimetic generates nociceptive effects [ 14 ].
As for the BDNF, the majority of reports suggest that the both pathways are significant for neuronal survival [ 23 - 25 ]. Therefore, activation of both the PI3K/AKT and MAPK/ERK by BDNF mimetics led to more therapeutic efficacy than selective PI3K/AKT activation. Furthermore BDNF-stimulated MAPK/ERK pathway involved in the regulation of neurogenesis and neuroplasticity, which are the two types of cellular events that take part in recovery after a stroke. Previously GSB-106 was shown to stimulate hippocampal neurogenesis in adult stressed mice [ 26 ].
In a series of experiments to study the neuroprotectie effects of GK-2 with the treatment beginning within different time after reperfusion it was determined that dipeptide had a wide “therapeutic window”. GK-2 significantly decreased infarct volumes (by 20% - 70%) in all the cases (Figure 3, Table 3). The maximum effect of GK-2 was recorded with the treatment beginning 6 and 8 h after surgery. Under these conditions GK-2 decreased cerebral infarct volume by 70% and 60% respectively. The neuroprotective effect of GK-2 still persisted with the 24 h therapeutic time window, although it became much less pronounced (reduction of infarct volume by 18%).
(A) (B) (C)
Figure 3. Dimeric dipeptide NGF mimetic GK-2 reduces cerebral infarct volume after transient middle cerebral artery occlusion in Wistar rats at different therapeutic time windows (A-6 h, B-8 h, C-24 h). Scatter dot plots (median with interquartile range) of cerebral infarct volumes (mm3). *p < 0.05 vs. the MCAO group (Mann-Whitney test), #p = 0.05 vs the MCAO group (Fisher exact test).
Table 3. Dimeric dipeptide NGF mimetic GK-2 reduces cerebral infarct volume after transient middle cerebral artery occlusion in Wistar rats at different therapeutic time windows.
Notes: The data are presented as medians and interquartile ranges; *p < 0.05 vs. the MCAO group (Mann-Whitney test), #p = 0.05 vs. the MCAO group (Fisher exact test).
The effectiveness of GK-2 at a delayed start of administration suggests that the dipeptide has neuroregenerative properties. These properties may be due to the stimulation of BDNF expression. There is literature data that NGF can stimulate the expression of BDNF [ 27 ]. It was revealed that GK-2, similar to NGF, stimulates BDNF expression (from T. A. Antipova).
The results obtained suggest a potential role for the dimeric dipeptide NGF and BDNF mimetics as a therapeutic agent useful for the treatment of a stroke.
This work was supported by the Russian Science Foundation (Project 18-15-00381) and Russian Foundation for Basic Research (Project 18-015-00228).
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