Journal of Traditional Chinese Medicine ›› 2022, Vol. 42 ›› Issue (5): 781-787.DOI: 10.19852/j.cnki.jtcm.20211214.002
• Research Articles • Previous Articles Next Articles
HU Xijiao1, CHENG Yinglong2, KANG Huanan3, LI Shuoxi4, WANG Yawen5, LIU Jinzhe6, SUN Yiming7(
), LIU Li8(
)
Received:2021-06-12
Accepted:2021-09-21
Online:2022-10-15
Published:2021-12-14
Contact:
SUN Yiming,LIU Li
About author:Dr. LIU Li, Endoscopy room, the First Affiliated Hospital of Heilongjiang University of Traditional Chinese Medicine, Hysteroscopy Department, Harbin 150040, China. lunwenfabiao2021@163.com Telephone: +86-15045023666Supported by:HU Xijiao, CHENG Yinglong, KANG Huanan, LI Shuoxi, WANG Yawen, LIU Jinzhe, SUN Yiming, LIU Li. Electroacupuncture attenuates chronic salpingitis via transforming growth factor-β1/p38 mitogen-activated protein kinase signaling pathway[J]. Journal of Traditional Chinese Medicine, 2022, 42(5): 781-787.
| Gene | Forward sequence | Reverse primer |
|---|---|---|
| GAPDH | F: TGGCCTTCCGTGTTCCTAC | R: GAGTTGCTGTTGAAGTCGCA |
| TGF-β1 | F: ATTCCTGGCGTTACCTT | R: AGCCCTGTATTCCGTCT |
Table 1 Primers sequences
| Gene | Forward sequence | Reverse primer |
|---|---|---|
| GAPDH | F: TGGCCTTCCGTGTTCCTAC | R: GAGTTGCTGTTGAAGTCGCA |
| TGF-β1 | F: ATTCCTGGCGTTACCTT | R: AGCCCTGTATTCCGTCT |
Figure 1 Effect of EA on the pathological changes in oviduct A-C: HE staining was used to observes the pathological changes (× 100); D-E: Masson staining was used to observe the collagen deposition which showed show blue (× 100); G: collagen area was counted by Image pro software. HE: hematoxylin-eosin; EA: electroacupuncture. Data are expressed as mean ±?standard deviation of three independent experiments. aP?<?0.05 compared with Normal group; bP?<?0.05 compared with Model group.
Figure 2 Effect of EA on the expressions of TGF-β1 A-I: expression of TGF-β1 was measured Immunofluorescence technique. The red color represents TGF-β1 staining, the blue color represents nuclei staining, and the cyan (red-blue) color represents nuclear translocation (original magnification, × 200); J-K: expression of TGF-β1 was measured by immunohistochemical analysis (× 200, brown yellow granules indicate positive reaction); M: The expression of TGF-β1 were counted by Image pro software; N-P: expression of TGF-β1 in serum and oviduct tissue were measured by ELISA kit and WB methods, respectively; Q: TGF-β1 mRNA expression was detected by RT-PCR. TGF-β1: transforming growth factor beta-1; ELISA: enzyme-linked immunosorbent assay; RT-PCR: reversetranscription-polymerase chain reaction; EA: electro-acupuncture. Data are expressed as mean?±?standard deviation of three independent experiments. aP?<?0.01 compared with Normal group; bP?<?0.01 compared with Model group.
Figure 3 EA regulated the p38 signaling way A-I: expression of p-P38 was measured Immunofluorescence technique. The red color represents p-P38 staining, the blue color represents nuclei staining, and the cyan (red-blue) color represents nuclear translocation (original magnification, ×200); J-O: expression of P38 and p-P38 were measured by immunohistochemical analysis (×200, brown yellow granules indicate positive reaction); P-Q: expression of P38 and p-P38 were counted by Image pro software; R: expression of p-P38 and P38 protein in oviduct tissue were measured by WB; S: p-P38/P38 expression was detected was counted. WB: Western blot; EA: electro-acupuncture. Data are expressed as mean?±?standard deviation of three independent experiments. aP?<?0.01 compared with Normal group; bP?<?0.01 compared with Model group.
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