Journal of Traditional Chinese Medicine ›› 2024, Vol. 44 ›› Issue (6): 1177-1186.DOI: 10.19852/j.cnki.jtcm.2024.06.006
• Research Articles • Previous Articles Next Articles
LIAO Mengting1, LI Tao2, CHU Fuhao2,3, CHEN Yan2, LOU Ni1, ZHUANG Yuan1, BO Rongqiang1, DING Xia2()
Received:
2024-02-18
Accepted:
2024-08-21
Online:
2024-12-15
Published:
2024-11-12
Contact:
DING Xia
About author:
Prof. Xia Ding, School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing 100010, China. dingx@bucm.edu.cn Telephone: +86-18811016240Supported by:
LIAO Mengting, LI Tao, CHU Fuhao, CHEN Yan, LOU Ni, ZHUANG Yuan, BO Rongqiang, DING Xia. Weichang’ an pill (胃肠安丸) alleviates functional dyspepsia through modulating brain-gut peptides and gut microbiota[J]. Journal of Traditional Chinese Medicine, 2024, 44(6): 1177-1186.
Figure 1 WCAP improves gastrointestinal motility in FD rats A: representative hematoxylin-eosin staining of stomach samples from each group, Magnification × 200, Scar bar = 100 μm. A1: Control group; A2: Model group; A3: WC1 group; A4: WC2 group; A5: WC3 group; A6: WC4 group; A7: WC5 group; A8: Dom group. B: representative appearance of small intestine in each group. B1: Control group; B2: Model group; B3: WC1 group; B4: WC2 group; B5: WC3 group; B6: WC4 group; B7: WC5 group; B8: Dom group. Control group and Model group were given normal saline for seven consecutive days; WC1 group: FD rat treated with 21.60 mg·kg-1·d-1 WCAP for seven days; WC2 group: FD rat treated with 43.20 mg·kg-1·d-1 WCAP for seven days; WC3 group: FD rat treated with 64.80 mg·kg-1·d-1 WCAP for seven days; WC4 group: FD rat treated with 86.40 mg·kg-1·d-1 WCAP for seven days; WC5 group: FD rat treated with 108.00 mg·kg-1·d-1 WCAP for seven days; Dom group: FD rat treated with 2.70 mg·kg-1·d-1 domperidone for seven days. FD: Functional dyspepsia; WCAP: Weichang’an pill; WC1: WCAP1; WC2: WCAP2; WC3: WCAP3; WC4: WCAP4; WC5: WCAP5.
Group | n | Gastric residual rates | Intestinal propulsion rate |
---|---|---|---|
Control | 10 | 54±6 | 81±5 |
Model | 10 | 79±6a | 67±5a |
WC1 | 10 | 68±12b | 74±5b |
WC2 | 10 | 67±4b | 74±5b |
WC3 | 10 | 63±14c | 80±5d |
WC4 | 10 | 67±12b | 76±8c |
WC5 | 10 | 64±13c | 76±9c |
Dom | 10 | 63±11c | 77±11c |
Table 1 Gastric residual rate and Intestinal propulsion rate of rats in each group (%,$\bar{x}±s$)
Group | n | Gastric residual rates | Intestinal propulsion rate |
---|---|---|---|
Control | 10 | 54±6 | 81±5 |
Model | 10 | 79±6a | 67±5a |
WC1 | 10 | 68±12b | 74±5b |
WC2 | 10 | 67±4b | 74±5b |
WC3 | 10 | 63±14c | 80±5d |
WC4 | 10 | 67±12b | 76±8c |
WC5 | 10 | 64±13c | 76±9c |
Dom | 10 | 63±11c | 77±11c |
Group | n | MTL | GAS | SS | VIP |
---|---|---|---|---|---|
Control | 10 | 225±19 | 160±19 | 54±5 | 124±16 |
Model | 10 | 138±34a | 99±29a | 84±10a | 231±19a |
WC1 | 10 | 191±39b | 115±27 | 80±6 | 201±24c |
WC2 | 10 | 193±31b | 117±32 | 76±8d | 187±24b |
WC3 | 10 | 204±31b | 127±21c | 69±8b | 199±19b |
WC4 | 10 | 193±27b | 123±18d | 65±9b | 186±18b |
WC5 | 10 | 194±23b | 140±20b | 62±7b | 162±15b |
Dom | 10 | 208±34b | 142±16b | 63±8b | 178±18b |
Table 2 Secretion of BGPs in each group (pg/mL, $\bar{x}±s$)
Group | n | MTL | GAS | SS | VIP |
---|---|---|---|---|---|
Control | 10 | 225±19 | 160±19 | 54±5 | 124±16 |
Model | 10 | 138±34a | 99±29a | 84±10a | 231±19a |
WC1 | 10 | 191±39b | 115±27 | 80±6 | 201±24c |
WC2 | 10 | 193±31b | 117±32 | 76±8d | 187±24b |
WC3 | 10 | 204±31b | 127±21c | 69±8b | 199±19b |
WC4 | 10 | 193±27b | 123±18d | 65±9b | 186±18b |
WC5 | 10 | 194±23b | 140±20b | 62±7b | 162±15b |
Dom | 10 | 208±34b | 142±16b | 63±8b | 178±18b |
Figure 2 Effect of WCAP on the diversity of gut microbiota in rats with FD A: venn diagram; B: species accumulation curves; C: Chao diversity index; D: simpson diversity index; E: Shannon diversity index; F: observed-species diversity index. Control: FD rat with normal saline; Model: FD rat with normal saline; WCAP: FD rat treated with 64.80 mg·kg-1·d-1 WCAP for seven days. FD: functional dyspepsia; WCAP: Weichang’an pill; OTU: operational taxonomic units. Dates were analyzed by one-way analysis of variance (n = 10). aP < 0.01, cP < 0.001 versus the control group; bP < 0.01, dP < 0.001, versus the model group.
Figure 3 Effect of WCAP on the structure of the gut microbiota in rats with FD A: phylum level species barplot; B: ratio of Firmicutes/Bacteroidetes; C: class level species barplot; D: order level species barplot; E: genus level species barplot; F: partial least squares discriminant analysis diagram of three groups. Control: FD rat with normal saline; Model: FD rat with normal saline; WCAP: FD rat treated with 64.80 mg·kg-1·d-1 WCAP for seven days. FD: functional dyspepsia; WCAP: Weichang’an pill; PLS-DA: partial least squares discriminant analysis; F/B: Firmicutes/Bacteroidetes.
Figure 4 LEfSe analysis and spearman correlation analysis between gut microbiota and BGPs A: bar graph of LEfSe analysis among the control group, the model group and the WCAP group. B: cladogram graph of LEfSe analysis among the control group, the model group and the WCAP group. C: Spearman correlation analysis was performed between the relative abundance of differential bacteria and the levels of MTL, GAS, SS, VIP. Control: FD rat with normal saline; Model: FD rat with normal saline; WCAP: FD rat treated with 64.80 mg·kg-1·d-1 WCAP for seven days. FD: functional dyspepsia; WCAP: Weichang’an pill; MTL: motilin; GAS: gastrin; SS: somatostatin; VIP: vasoactive intestinal peptide; LEfSe: linear discriminant analysis effect size.
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