Figures & data
![](/cms/asset/021ed764-7c44-46af-a0ae-a716b6d220de/tbbb_a_1413325_uf0001_b.gif)
Figure 1. BBB permeability of IDP and activation of neuronal cells by carnosine. (A) BBB permeability of IDP. BBB permeability of IDP was assessed using a BBB kit and estimated by the resulting permeability coefficient (Papp). (B) Activation of SH-SY5Y cells by carnosine. Carnosine was added to SH-SY5Y cells, and neurite (arrow) growth was observed by fluorescence microscopy (BZ-X700, Keyence, Osaka, Japan).
![Figure 1. BBB permeability of IDP and activation of neuronal cells by carnosine. (A) BBB permeability of IDP. BBB permeability of IDP was assessed using a BBB kit and estimated by the resulting permeability coefficient (Papp). (B) Activation of SH-SY5Y cells by carnosine. Carnosine was added to SH-SY5Y cells, and neurite (arrow) growth was observed by fluorescence microscopy (BZ-X700, Keyence, Osaka, Japan).](/cms/asset/bc44ec16-a028-4a1c-a04b-e6d5522a59ba/tbbb_a_1413325_f0001_oc.gif)
Figure 2. Carnosine augments the expression of neurotrophin genes. The effects of carnosine on expression of BDNF in U-87 MG cells (A) and SH-SY5Y cells (B) were evaluated by qRT-PCR. The effects of carnosine on the expression of NGF (C and D), NTF4 (E and F) and GDNF (G and H) in U-87 MG cells and SH-SY5Y cells, respectively, were also evaluated by qRT-PCR.
![Figure 2. Carnosine augments the expression of neurotrophin genes. The effects of carnosine on expression of BDNF in U-87 MG cells (A) and SH-SY5Y cells (B) were evaluated by qRT-PCR. The effects of carnosine on the expression of NGF (C and D), NTF4 (E and F) and GDNF (G and H) in U-87 MG cells and SH-SY5Y cells, respectively, were also evaluated by qRT-PCR.](/cms/asset/76391bcf-5e47-4516-902f-3d2fefbe61ff/tbbb_a_1413325_f0002_b.gif)
Figure 3. Carnosine activates BDNF production in U-87 MG cells. U-87 MG cells were treated with 10 mM carnosine for 3 days. BDNF in the supernatant was assessed using an ELISA kit (Promega).
![Figure 3. Carnosine activates BDNF production in U-87 MG cells. U-87 MG cells were treated with 10 mM carnosine for 3 days. BDNF in the supernatant was assessed using an ELISA kit (Promega).](/cms/asset/2f43f608-ac50-4323-97f0-50ef017ab142/tbbb_a_1413325_f0003_b.gif)
Figure 4. Carnosine promotes neurite outgrowth in neuronal cells via glial cells. After U-87 MG cells were treated with 5 mM carnosine for 24 h, supernatant was collected and added to SH-SY5Y cells. BDNF (100 ng/mL) was used as a positive control. Cells were stained with Milli-Mark FluoroPan Neuronal Marker (A). Neurite length was determined using a Neurite Outgrowth Assay kit (B).
![Figure 4. Carnosine promotes neurite outgrowth in neuronal cells via glial cells. After U-87 MG cells were treated with 5 mM carnosine for 24 h, supernatant was collected and added to SH-SY5Y cells. BDNF (100 ng/mL) was used as a positive control. Cells were stained with Milli-Mark FluoroPan Neuronal Marker (A). Neurite length was determined using a Neurite Outgrowth Assay kit (B).](/cms/asset/e958c86f-f2d3-4a96-b6d2-7cfedd0d5e23/tbbb_a_1413325_f0004_b.gif)