Evidence Details for Il16
PMID Title Journal Year Abstract
35722406 Electroacupuncture of the Baihui and Shenting acupoints for vascular dementia in rats through the miR-81/IL-16/PSD-95 pathway. Ann Transl Med. 2022 May;10(10):540. doi: 10.21037/atm-22-2068. 2022 May BACKGROUND: There is currently no effective treatment for vascular dementia (VaD). Scalp electroacupuncture (EA) has served clinically as an alternative treatment for VaD, but its mechanism is still unclear. In this study, we investigated the effect of EA at the Baihui (GV 20) and Shenting (GV 24) acupoints on spatial learning and memory ability, and the expression level of microRNA-81 (miR-81), interleukin-16 (IL-16), and postsynaptic density protein-95 (PSD-95) in the frontal cortex of VaD rats. METHODS: Male Sprague-Dawley rats were randomly divided into four groups, sham, VaD, non-acupuncture (non-AP) and EA group. The VaD model was established by permanent bilateral occlusion of the common carotid arteries. Morris Water Maze was used to assess the rats' spatial learning and memory. Immunochemistry (IHC), quantitative reverse transcription polymerase chain reaction (qRT-PCR), and western blot analysis were performed to detect the expression level of miR-81, IL-16, and PSD-95. Finally, luciferase assay was used to determine the effect of miR-81 on IL-16 expression in PC12 cells. RESULTS: The space exploration experiment of MWM showed the time and distance of the rat's activities around the platform were decreased in the EA group. Compared to the VaD and non-AP group, the number of terminal deoxynucleotidyl transferase-mediated dUDP nick-end labeling (TUNEL)-positive frontal cortical neurons was significantly decreased in EA group. The number of the PSD-95-positive cells and the miR-81 expression level in the frontal cortical in the EA group was dramatically increased in comparison with the other groups. In the PC12 cell validation experiment, IL-16 expression level was reduced under the condition of the miR-81 mimic treatment, while increased in the miR-81 inhibitor group. The PSD-95 protein level was up-regulated in the small interfering (si)RNA-IL16 group compared to the NC-IL16 groups with or without oxygen/glucose deprivation/reperfusion (OGD/R) conditions (P<0.05). However, this was abolished by miR-81 mimic. CONCLUSIONS: In VaD rats, EA may improve spatial learning and memory through miR-81/IL-16/PSD-95 pathway."

Evidence Sentence: The PSD-95 protein level was up-regulated in the small interfering (si)RNA-IL16 group compared to the NC-IL16 groups with or without oxygen/glucose deprivation/reperfusion (OGD/R) conditions (P<0.05).
Evidence Sentence: Western blot analysis revealed PSD-95 protein levels were increased in the si-IL16 group compared to the NC-IL16 group in or not in OGD/R conditions (P<0.05) (Figure 6), but the overall levels of both were reduced in OGD/R conditions (P<0.01).
Evidence Sentence: NC-IL16 + NC-mimic + NC-inhibitor + OGD group), but in the absence of IL-16, PSD-95 was downregulated in cells treated with miR-81 mimic (i.e., NC-IL16 + mimic + NC-inhibitor + OGD vs.
Evidence Sentence: Si-IL16 + mimic + NC-inhibitor + OGD; P<0.05).
Evidence Sentence: IL-16 is a potential target of miR-81
Evidence Sentence: In this study, we investigated the effect of EA at the Baihui (GV 20) and Shenting (GV 24) acupoints on spatial learning and memory ability, and the expression level of microRNA-81 (miR-81), interleukin-16 (IL-16), and postsynaptic density protein-95 (PSD-95) in the frontal cortex of VaD rats.
Evidence Sentence: Immunochemistry (IHC), quantitative reverse transcription polymerase chain reaction (qRT-PCR), and western blot analysis were performed to detect the expression level of miR-81, IL-16, and PSD-95.
Evidence Sentence: Finally, luciferase assay was used to determine the effect of miR-81 on IL-16 expression in PC12 cells.
Evidence Sentence: In the PC12 cell validation experiment, IL-16 expression level was reduced under the condition of the miR-81 mimic treatment, while increased in the miR-81 inhibitor group.
Evidence Sentence: Binding sites in the miR-81 sequence (5'-GUCAGUG-3') and the IL-16 gene sequence (5'-CAGUCAC-3') were predicted via bioinformatics analysis (Figure 5A).
Evidence Sentence: To evaluate the direct effects of miR-81 on IL-16 gene expression, we constructed a dual luciferase reporter carrying the miR-81 target site in pLUC-IL-16 (Figure 5B).
Evidence Sentence: The data indicated that the miR-81 mimic decreased the luciferase activity of IL-16.
Evidence Sentence: Contrastingly, the miR-81 mimic did not decrease activity of luciferase while the miR-81 seed sequence of the IL-16 3'UTR was mutated (Figure 5C).
Evidence Sentence: To further assess the relationship between miR-81 and IL-16, PC12 cells were divided into 4 groups: miR-81 mimic, miR-81 mimic-NC, miR-81 inhibitor, and miR-81 inhibitor-NC.
Evidence Sentence: After transfecting PC12 cells with miR-81 mimic, miR-81 mimic-NC, miR-81 inhibitor, and miR-81 inhibitor-NC, the relative expression of IL-16 mRNA was measured using RT-qPCR.
Evidence Sentence: Overall, IL-16 expression was decreased in the mimic group compared to the mimic-NC group and increased in the inhibitor group compared to the inhibitor-NC group (Figure 5E).
Evidence Sentence: These results indicate that miR-81 directly regulates IL-16.
Evidence Sentence: To determine whether IL-16 mediates the effect of miR-81 on regulation of PSD-95, IL-16 expression was silenced in PC12 cells subjected to oxygen glucose deprivation/reperfusion (OGD/R) injury and followed by miR-81 mimic/inhibitor treatment.
Evidence Sentence: NC-IL16 + NC-mimic + NC-inhibitor + OGD group), but in the absence of IL-16, PSD-95 was downregulated in cells treated with miR-81 mimic (i.e., NC-IL16 + mimic + NC-inhibitor + OGD vs.
Evidence Sentence: These results indicate that IL-16 is required for the effects of miR-81 for the regulation of PSD-95 in OGD/R injury.
Evidence Sentence: Interleukin-16 mediates the effect of miR-81 on regulation of PSD-95
Evidence Sentence: Electroacupuncture of the Baihui and Shenting acupoints for vascular dementia in rats through the miR-81/IL-16/PSD-95 pathway
Evidence Sentence: In VaD rats, EA may improve spatial learning and memory through miR-81/IL-16/PSD-95 pathway.