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Editor-in-ChiefWU Yiling
Supervisor

National Administration of Traditional Chinese Medicine
Sponsor

Institute of Traditional Chinese MedicineChina Academy of Chinese Medical SciencesChina Association of Chinese Medicine

CN11-3495/R

ISSN1005-9903(Print)

ISSN:2097-1494(Online)

Composite impact factor

5.474(CNKI)

Publication CycleSemimonthly

AddressNo.16Nanxiao StreetDongzhimenDongcheng DistrictBeijing

Tel010-84076882

E-mailsyfjx_2010@188.com

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Exploration of Mechanism of Guipitang on Mitochondrial Biogenesis of Hippocampal Neurons in MMA Rats Based on AMPK/PGC-1α Signaling Pathway

ObjectiveTo investigate the mechanism by which Guipitang regulates mitochondrial biogenesis of hippocampal neurons in methylmalonic aciduria (MMA) rats through the adenosine monophosphate-activated protein kinase/peroxisome proliferator-activated receptor gamma coactivator 1α (AMPK/PGC-1α) signaling pathway.MethodsFifty 5-day-old Wistar rats were randomly divided into a blank group, a model group, a Guipitang group (9.3 g·kg-1), an AMPK inhibitor group (2.5 mg·kg-1 Compound C), and a Guipitang + AMPK inhibitor group (9.3 g·kg-1 + 2.5 mg·kg-1 Compound C) using a random number table method. After 3 weeks of administration, the Morris water maze test was used to assess the rats' learning and memory abilities. Hematoxylin-eosin (HE), Nissl, and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) staining was performed to detect histopathological changes and apoptosis in rat hippocampal tissue. Colorimetric assays were employed to measure mitochondrial adenosine triphosphate (ATP) content in hippocampal tissue. The mitochondrial superoxide red fluorescent probe method (MitoSOX Red) was used to assess mitochondrial reactive oxygen species (ROS) levels. The JC-1 assay was carried out to detect mitochondrial membrane potential in hippocampal tissue. Transmission electron microscopy (TEM) was conducted to observe pathological changes in mitochondria. Real-time quantitative polymerase chain reaction (Real-time PCR) was used to detect mitochondrial DNA copy numbers. Western blot was employed to detect AMPK, PGC-1α, phosphorylated AMPK (p-AMPK), nuclear factor E2-related factor 1 (Nrf1), nuclear factor E2-related factor 2 (Nrf2), and mitochondrial transcription factor A (TFAM) in rat hippocampal tissue.ResultsCompared with those in the blank group, rats in the model group exhibited more dispersed movement paths, were unable to locate the platform independently, and had prolonged escape latency, reduced frequency of crossing the platform, significantly reduced time spent in the target quadrant, and significantly increased time spent in the opposite quadrant (P<0.01). Compared with those in the model group, rats in the Guipitang group and the Guipitang + AMPK inhibitor group had significantly shortened escape latency, significantly increased frequency of crossing the platform, significantly increased time spent in the target quadrant, and significantly reduced time spent in the opposite quadrant (P<0.05, P<0.01). Compared with the Guipitang group, the AMPK inhibitor group had a longer escape latency, significantly reduced frequency of crossing the platform, significantly reduced time spent in the target quadrant, and significantly increased time spent in the opposite quadrant (P<0.01). The model group showed disorganized arrangement of hippocampal neurons and nuclear pyknosis. After treatment with Guipitang, the number of regular neurons increased, while the improvement in the Guipitang + AMPK inhibitor group was less than that in the Guipitang group (P<0.01). Electron microscopy showed that the cristae structure of mitochondria was extensively lost in the model group, but significantly recovered in the Guipitang group (P<0.01). The Guipitang + AMPK inhibitor group still exhibited mitochondrial membrane rupture and reduced cristae structure. The apoptosis rate was significantly increased in the model group. Compared with the blank group, the model group had significantly increased ROS levels, significantly reduced ATP content, and significantly decreased mitochondrial membrane potential (P<0.01). Compared with the model group, the Guipitang group had significantly reduced ROS levels, significantly increased ATP content, and significantly increased mitochondrial membrane potential (P<0.01). Compared with the model group, the Guipitang group showed a significant decrease in apoptosis rate (P<0.01), and this effect was partially reversed by the AMPK inhibitor (P<0.01). The model group showed significantly reduced TFAM, PGC-1α, Nrf1, and Nrf2 mRNA expression and protein expression levels (P<0.01). Compared with the model group, the Guipitang group showed significantly increased TFAM, PGC-1α, Nrf1, and Nrf2 mRNA expression and protein expression levels (P<0.01). Compared with the blank group, the model group showed significantly reduced p-AMPK/AMPK protein expression levels (P<0.01). Compared with the model group, the Guipitang group showed significantly increased p-AMPK/AMPK protein expression levels (P<0.01).ConclusionGuipitang can improve cognitive dysfunction in rats by activating the AMPK/PGC-1α signaling pathway, promoting mitochondrial biogenesis, and alleviating pathological damage to hippocampal neurons.

Exploration of Mechanism of Guipitang on Mitochondrial Biogenesis of Hippocampal Neurons in MMA Rats Based on AMPK/PGC-1<italic>α</italic> Signaling Pathway
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Volume 32  Issue 20,2026

    DU Xuqin, LI Yixuan, JIN Yuxia, LI Hongding, YANG Ruogu, SHI Lipeng, REN Yi

    Vol. 32, Issue 20, Pages: 1-10(2026) DOI: 10.13422/j.cnki.syfjx.20260442
    Abstract:ObjectiveTo investigate the effects and mechanisms of Fangji Fulingtang (FFD) on mitochondrial function in the mouse model of myocardial fibrosis (MF).MethodsSixty SPF-grade male C57BL/6J mice were randomly allocated into six groups (n=10 per group): control, model, low-dose, medium-dose, and high-dose (3.315, 6.63, and 13.26 g·kg-1, respectively) FFD, and captopril (20 mg·kg-1). MF was induced by subcutaneous injection of isoproterenol (10 mg·kg-1·d-1) in other groups except the control group for 14 consecutive days, with simultaneous gavage of corresponding drugs. Left ventricular ejection fraction (LVEF) and left ventricular fractional shortening (LVFS) were measured by echocardiography. Serum levels of creatine kinase-MB (CK-MB), cardiac troponin I (cTnI), N-terminal pro-brain natriuretic peptide (NT-pro BNP), tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), and interleukin-6 (IL-6) were determined by enzyme-linked immunosorbent assay (ELISA). Malondialdehyde (MDA), superoxide dismutase (SOD), and glutathione (GSH) levels were measured by biochemical assays. Reactive oxygen species (ROS) were detected by dihydroethidium (DHE) fluorescence staining. Hematoxylin-eosin (HE), Masson's trichrome, and wheat germ agglutinin (WGA) staining were performed to evaluate myocardial structure and fibrosis. Mitochondrial ultrastructure and function were assessed by transmission electron microscopy, adenosine triphosphate (ATP) colorimetric assay, and JC-1 fluorescence staining. The protein levels of phosphorylated adenosine monophosphate-activated protein kinase α subunit (p-AMPKα), AMPKα, peroxisome proliferator-activated receptor gamma coactivator-1α (PGC-1α), mitofusin 2 (MFN2), pyruvate kinase M2 isoform (PKM2), lactate dehydrogenase A (LDHA), and hypoxia-inducible factor 1 alpha (HIF-1α) were analyzed by Western blot.ResultsCompared with the control group, the model group exhibited decreased LVEF and LVFS, increased heart weight index and heart weight-to-tibia length ratio (P<0.01), elevated levels of myocardial injury markers (CK-MB, cTnI, and NT-pro BNP), inflammatory cytokines (TNF-α, IL-1β, and IL-6), and MDA, along with reduced SOD and GSH levels (P<0.01). Enhanced interstitial collagen deposition and cardiomyocyte hypertrophy were observed in the model group (P<0.01). Transmission electron microscopy and JC-1 staining revealed mitochondrial swelling, crista disruption, decreased ATP content, and reduced red/green fluorescence ratio in the model group (P<0.01). Western blot analysis demonstrated downregulation of p-AMPKα, PGC-1α, and MFN2 and upregulation of PKM2, LDHA, and HIF-1α in the model group (P<0.01). Compared with the model group, treatment with FFD or captopril improved LVEF and LVFS, reduced heart weight index and heart weight-to-tibia length ratio (P<0.05, P<0.01), lowered the serum levels of CK-MB, cTnI, NT-pro BNP, TNF-α, IL-1β, IL-6, and MDA, increased the SOD and GSH levels (P<0.05, P<0.01), attenuated the myocardial fibrosis and cardiomyocyte hypertrophy (P<0.01), and restored the mitochondrial ultrastructure. The medium and high-dose FFD groups as well as the captopril group showed increased ATP production and red/green fluorescence ratio (P<0.05, P<0.01). Furthermore, FFD upregulated the expression of p-AMPKα and PGC-1α while downregulating the expression of LDHA and HIF-1α (P<0.05, P<0.01).ConclusionFFD activates the AMPK/PGC-1α/MFN2 signaling pathway and inhibits the PKM2/LDHA/HIF-1α axis to restore mitochondrial function and energy metabolic homeostasis, thereby attenuating isoproterenol-induced myocardial fibrosis.  
    Keywords:Fangji Fulingtang;myocardial fibrosis;mitochondrial function;adenosine monophosphate-activated protein kinase (AMPK)/peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α)/mitofusin 2 (MFN2)-pyruvate kinase M2 isoform (PKM2) signaling pathway;energy metabolism  
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    Updated:2026-09-17

    ZHANG Ge, ZHAO Chunlin, PAN Li, ZHANG Ying, CHEN Zehai, ZHANG Siya, FANG Yiming, SHI Wei

    Vol. 32, Issue 20, Pages: 11-21(2026) DOI: 10.13422/j.cnki.syfjx.20260565
    Abstract:ObjectiveTo investigate the protective effect of Qiju Dihuang Wan on diabetic retinopathy (DR) and its regulatory mechanism on the NOD-like receptor protein 3/Cysteinyl aspartate-specific proteinase-1/Gasdermin D (NLRP3/Caspase-1/GSDMD) signaling pathway.MethodsHuman retinal microvascular endothelial cells (HRMEC) were divided into the blank group, model group, and Qiju Dihuang Wan low- and high-dose groups. Except for the blank group, all groups were induced with 40 mmol·L-1 high glucose, and the treatment groups were supplemented with 6% and 12% Qiju Dihuang Wan-containing serum, respectively, based on the induction. After 24 h of culture, the levels of interleukin (IL)-1β and IL-18 were measured by enzyme-linked immunosorbent assay (ELISA), pyroptosis-related protein expression was detected by immunofluorescence and Western blot, and the mRNA levels of NLRP3/Caspase-1/GSDMD signaling pathway-related molecules were determined by real-time polymerase chain reaction (Real-time PCR). The mice were randomly divided into the blank group, model group, Qiju Dihuang Wan low-, medium-, and high-dose groups (11, 22, 44 g·kg-1·d-1), and calcium dobesilate group (0.13 g·kg-1·d-1). Except for the blank group, all groups were intraperitoneally injected with streptozotocin to establish the DR model. After successful modeling, the treatment groups received corresponding doses of Qiju Dihuang Wan crude drug or calcium dobesilate suspension by gavage once daily, while the blank group and model group received an equal volume of normal saline, for 8 consecutive weeks. Fundus changes were examined by optical coherence tomography, optical coherence tomography angiography, and fundus fluorescein angiography. Retinal pathological morphology was observed by hematoxylin-eosin staining. Real-time PCR was used to detect the mRNA levels of NLRP3, Caspase‑1, GSDMD, IL‑1β, and IL‑18 in retinal tissue, and Western blot was used to detect the protein expression of NLRP3, ASC, cleaved Caspase‑1, and GSDMD‑N.ResultsCell experiments showed that compared with the blank group, the model group showed significantly decreased HRMEC viability (P<0.01), and significantly increased levels of IL-1β, IL-18, as well as increased protein expression of NLRP3, cleaved Caspase-1, and GSDMD-N (P<0.01). Compared with the model group, the above indicators were significantly reduced in the high-dose Qiju Dihuang Wan groups (P<0.05, P<0.01). Animal experiments showed that compared with the blank group, the model group had elevated blood glucose (P<0.01), decreased retinal thickness and vascular density (P<0.01), up‑regulated mRNA expression of NLRP3, Caspase‑1, GSDMD, IL‑1β and IL‑18 in retinal tissue (P<0.01), and up‑regulated protein expression of NLRP3, ASC, cleaved Caspase‑1 and GSDMD‑N (P<0.01). Compared with the model group, the Qiju Dihuang Wan medium- and high‑dose groups showed decreased blood glucose (P<0.01), increased retinal thickness and vascular density (P<0.01), alleviated retinal pathological damage, and down‑regulated mRNA expression of NLRP3, Caspase‑1, GSDMD, IL‑1β, IL‑18, as well as protein expression of NLRP3, ASC, cleaved Caspase‑1, and GSDMD‑N (P<0.05, P<0.01).ConclusionQiju Dihuang Wan may exert protective effects against diabetic retinopathy by inhibiting the activation of the NLRP3/Caspase-1/GSDMD signaling pathway and alleviating high glucose-induced retinal pyroptosis.  
    Keywords:Qiju Dihuang Wan;diabetic retinopathy;pyroptosis;NOD-like receptor family pyrin domain containing 3 (NLRP3) inflammasome;human retinal microvascular endothelial cell  
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    Updated:2026-09-17
    Abstract:ObjectiveTo investigate the mechanisms of Zuojinwan in the treatment of colorectal cancer from the perspective of inhibiting M2 polarization of tumor-associated macrophages.MethodsA colorectal cancer mouse model was established by azoxymethane (AOM)/dextran sulfate sodium (DSS). Body weight was recorded, disease activity index (DAI) and tumor number were calculated, and hematoxylin-eosin (HE) staining was used to observe colonic pathological changes. Enzyme-linked immunosorbent assay (ELISA) was used to detect the levels of interleukin-6 (IL-6), transforming growth factor-β (TGF-β), interleukin-1β (IL-1β), and tumor necrosis factor-α (TNF-α) in colonic homogenates. Immunohistochemistry was used to detect proliferating cell nuclear antigen (PCNA) expression in the colon, and immunofluorescence was used to detect mannose receptor (CD206) expression in macrophages. In vitro, M2 macrophages were induced using IL-4/IL-13, and macrophages were treated with different concentrations of Zuojinwan-containing serum. CD206 and differentiation cluster 86 (CD86) were analyzed by flow cytometry. A CT26 and RAW264.7 macrophage co-culture system was established, and the migration and proliferation abilities of CT26 cells were detected using Transwell assays and trypan blue exclusion. Finally, proteomics was used to screen key proteins and signaling pathways involved in Zuojinwan-mediated inhibition of M2 polarization of tumor-associated macrophages in colorectal cancer, and Western blot was used for validation.ResultsIn animal experiments, compared with the blank group, mice in the model group showed significantly decreased body weight (P<0.05), significantly increased DAI scores (P<0.01), and significantly increased tumor number (P<0.01), with severe colonic carcinogenesis and lymphatic metastasis. The protein expression levels of PCNA and CD206 were significantly increased (P<0.01), and the levels of IL-6, IL-1β, TNF-α, and TGF-β in colonic homogenates were significantly increased (P<0.01). Compared with the model group, mice in the Zuojinwan intervention group showed significantly higher body weight (P<0.05), significantly decreased DAI scores (P<0.01), and significantly reduced tumor numbers (P<0.01). The protein levels of PCNA and CD206 were significantly decreased (P<0.05), and the levels of IL-6, IL-1β, TNF-α, and TGF-β in colonic homogenates were significantly decreased (P<0.05). In the CT26 and RAW264.7 co-culture system in vitro, compared with the blank group, co-culture with M2-type RAW264.7 macrophages significantly increased CT26 cell migration rate and proliferation number (P<0.01). Compared with the M2 group (M2-type macrophages), the proportion of CD86 was significantly increased in the Zuojinwan-containing serum group (P<0.01), while the CT26 cell migration rate and proliferation number were significantly decreased in the 8% Zuojinwan-containing serum group (P<0.01). Proteomics analysis indicated that tumor necrosis factor-α-induced protein 8-like protein 1 (TIPE1) may be a key target through which Zuojinwan regulates macrophage phenotypic transformation to inhibit colorectal cancer. The phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt) signaling pathway showed the highest enrichment. Compared with the blank group, the levels of TIPE1, p-PI3K, and p-Akt in M2 macrophages were significantly increased (P<0.05,P<0.01). After treatment with Zuojinwan-containing serum, the levels of TIPE1, p-PI3K, and p-Akt were significantly decreased (P<0.05,P<0.01).ConclusionZuojinwan may inhibit colorectal cancer proliferation and migration by suppressing M2 polarization of tumor-associated macrophages, which may be associated with inhibition of the PI3K/Akt signaling pathway in tumor-associated macrophages.  
    Keywords:Zuojinwan;formula;colorectal cancer;tumor-associated macrophages;tumor necrosis factor-α-induced protein 8-like protein 1 (TIPE1)/phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt)signaling pathway  
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