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Study on the Mechanism of Bu-Shen-He-Mai Granules in Improving Renal Damage of Ageing Spontaneously Hypertensive Rats by Regulating Th17 Cell/Tregs Balance

METHODS: Blood pressure and urine biochemical indices were recorded. Renal blood flow was evaluated by renal ultrasonography. Transmission electron microscopy (TEM) and HE staining were used to assess kidney and spleen morphology. Renal fibrosis was assessed using Masson staining. Serum levels of IL...

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Autores principales: Zhang, Peng, Song, Xu-Yu, Li, Wen, Wei, Jian-Liang, Cui, Yan-Jun, Qi, Ying-Zi, Chen, Xiu-Bao, Jiang, Yue-Hua, Yang, Chuan-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056229/
https://www.ncbi.nlm.nih.gov/pubmed/35502169
http://dx.doi.org/10.1155/2022/8315503
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author Zhang, Peng
Song, Xu-Yu
Li, Wen
Wei, Jian-Liang
Cui, Yan-Jun
Qi, Ying-Zi
Chen, Xiu-Bao
Jiang, Yue-Hua
Yang, Chuan-Hua
author_facet Zhang, Peng
Song, Xu-Yu
Li, Wen
Wei, Jian-Liang
Cui, Yan-Jun
Qi, Ying-Zi
Chen, Xiu-Bao
Jiang, Yue-Hua
Yang, Chuan-Hua
author_sort Zhang, Peng
collection PubMed
description METHODS: Blood pressure and urine biochemical indices were recorded. Renal blood flow was evaluated by renal ultrasonography. Transmission electron microscopy (TEM) and HE staining were used to assess kidney and spleen morphology. Renal fibrosis was assessed using Masson staining. Serum levels of IL-6, IL-10, and IL-17A were measured using ELISAs. The density of RORγ and Foxp3 in the spleen was observed by immunofluorescence staining. The levels of Th17 cells and Tregs in blood were detected via flow cytometry. Transcriptome sequencing was performed to screen the targets of BSHM granules in hypertensive kidneys. RESULTS: BSHM granules decreased SBP by 21.2 mm·Hg and DBP by 8.8 mm·Hg in ageing SHRs (P < 0.05), decreased the levels of urine mALB, β2-Mg, and NAG (P < 0.01), and improved renal blood flow and arteriosclerosis. BSHM granules increased IL-10 expression (P < 0.05) while decreasing IL-6 (P < 0.01) and IL-17A (P < 0.05) levels. BSHM granules improved Foxp3 density and the number of Tregs (P < 0.01) and reduced RORγt density and the number of Th17 cells (P < 0.01). Transcriptome sequencing identified 747 differentially expressed (DE) mRNAs in kidneys after BSHM treatment. GO analysis suggested that BSHM granules act through immunoregulation. CONCLUSIONS: BSHM granules attenuated hypertensive renal damage in ageing SHRs, by significantly increasing Tregs and decreasing Th17 cells.
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spelling pubmed-90562292022-05-01 Study on the Mechanism of Bu-Shen-He-Mai Granules in Improving Renal Damage of Ageing Spontaneously Hypertensive Rats by Regulating Th17 Cell/Tregs Balance Zhang, Peng Song, Xu-Yu Li, Wen Wei, Jian-Liang Cui, Yan-Jun Qi, Ying-Zi Chen, Xiu-Bao Jiang, Yue-Hua Yang, Chuan-Hua Evid Based Complement Alternat Med Research Article METHODS: Blood pressure and urine biochemical indices were recorded. Renal blood flow was evaluated by renal ultrasonography. Transmission electron microscopy (TEM) and HE staining were used to assess kidney and spleen morphology. Renal fibrosis was assessed using Masson staining. Serum levels of IL-6, IL-10, and IL-17A were measured using ELISAs. The density of RORγ and Foxp3 in the spleen was observed by immunofluorescence staining. The levels of Th17 cells and Tregs in blood were detected via flow cytometry. Transcriptome sequencing was performed to screen the targets of BSHM granules in hypertensive kidneys. RESULTS: BSHM granules decreased SBP by 21.2 mm·Hg and DBP by 8.8 mm·Hg in ageing SHRs (P < 0.05), decreased the levels of urine mALB, β2-Mg, and NAG (P < 0.01), and improved renal blood flow and arteriosclerosis. BSHM granules increased IL-10 expression (P < 0.05) while decreasing IL-6 (P < 0.01) and IL-17A (P < 0.05) levels. BSHM granules improved Foxp3 density and the number of Tregs (P < 0.01) and reduced RORγt density and the number of Th17 cells (P < 0.01). Transcriptome sequencing identified 747 differentially expressed (DE) mRNAs in kidneys after BSHM treatment. GO analysis suggested that BSHM granules act through immunoregulation. CONCLUSIONS: BSHM granules attenuated hypertensive renal damage in ageing SHRs, by significantly increasing Tregs and decreasing Th17 cells. Hindawi 2022-04-23 /pmc/articles/PMC9056229/ /pubmed/35502169 http://dx.doi.org/10.1155/2022/8315503 Text en Copyright © 2022 Peng Zhang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhang, Peng
Song, Xu-Yu
Li, Wen
Wei, Jian-Liang
Cui, Yan-Jun
Qi, Ying-Zi
Chen, Xiu-Bao
Jiang, Yue-Hua
Yang, Chuan-Hua
Study on the Mechanism of Bu-Shen-He-Mai Granules in Improving Renal Damage of Ageing Spontaneously Hypertensive Rats by Regulating Th17 Cell/Tregs Balance
title Study on the Mechanism of Bu-Shen-He-Mai Granules in Improving Renal Damage of Ageing Spontaneously Hypertensive Rats by Regulating Th17 Cell/Tregs Balance
title_full Study on the Mechanism of Bu-Shen-He-Mai Granules in Improving Renal Damage of Ageing Spontaneously Hypertensive Rats by Regulating Th17 Cell/Tregs Balance
title_fullStr Study on the Mechanism of Bu-Shen-He-Mai Granules in Improving Renal Damage of Ageing Spontaneously Hypertensive Rats by Regulating Th17 Cell/Tregs Balance
title_full_unstemmed Study on the Mechanism of Bu-Shen-He-Mai Granules in Improving Renal Damage of Ageing Spontaneously Hypertensive Rats by Regulating Th17 Cell/Tregs Balance
title_short Study on the Mechanism of Bu-Shen-He-Mai Granules in Improving Renal Damage of Ageing Spontaneously Hypertensive Rats by Regulating Th17 Cell/Tregs Balance
title_sort study on the mechanism of bu-shen-he-mai granules in improving renal damage of ageing spontaneously hypertensive rats by regulating th17 cell/tregs balance
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056229/
https://www.ncbi.nlm.nih.gov/pubmed/35502169
http://dx.doi.org/10.1155/2022/8315503
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