- Open Access
The tibetan medicine Zuozhu-Daxi can prevent Helicobacter pylori induced-gastric mucosa inflammation by inhibiting lipid metabolism
Chinese Medicine volume 17, Article number: 126 (2022)
Tibetan medicine has been used in clinical practice for more than 3800 years. Zuozhu-Daxi (ZZDX), a classic traditional Tibetan medicine, has been proved to be effective in the treatment of digestive diseases, such as chronic gastritis, gastric ulcer, etc. Helicobacter pylori (H. pylori), one of the most common pathogenic microbes, is regarded as the most common cause of gastritis. Researching on the effects of ZZDX on H. pylori-induced gastric mucosa inflammation could provide more evidences on H. pylori treatment and promote the development of Tibetan medicine. This study aimed to explore whether ZZDX could rescue H. pylori-induced gastric mucosa inflammation and its mechanism.
Male C57BL/6 mice were infected with H. pylori, and orally treated with ZZDX to rescue gastric mucosa inflammation induced by H. pylori infection. Pathology of gastric mucosa inflammation was evaluated under microscopy by hematoxylin–eosin (HE) staining. The infection status of H. pylori was evaluated by immunohistochemical (IHC) staining. The reactive oxygen species (ROS) level in serum was evaluated using a detection kit. IL-1α, IL-6, and PGE2 expression levels in serum were measured using ELISA. IL-1α, IL-8, TNF-α, and NOD1 expression levels in gastric tissues were measured using real-time PCR. RNA sequencing and gene certification of interest were performed to explore the mechanisms in vivo and in vitro.
The results showed that ZZDX could significantly inhibit H. pylori-induced gastric mucosa inflammation using HE staining. IL-1α, IL-6, and PGE2 expression levels in serum were significantly decreased after treatment with ZZDX. ZZDX treatment significantly decreased the mRNA expression of IL-8 induced by H. pylori infection in gastric tissues. Elovl4, Acot1 and Scd1 might be involved in the mechanisms of ZZDX treatment. However, the H. pylori infection status in the gastric mucosa was not reduced after ZZDX treatment.
ZZDX reversed gastric mucosal injury and alleviated gastric mucosa inflammation induced by H. pylori infection.
Helicobacter pylori (H. pylori), a gram-negative bacterium which colonizes approximately 50% of the population worldwide , is one of the most common pathogenic microbes and is regarded as the major cause of gastritis. It is well known that chronic infection of H. pylori can even lead to gastric precancerous lesions including mucosal atrophy and intestinal metaplasia, and thus long-term infection ultimately can result in gastric cancer . In 1994, H. pylori was defined as a class I carcinogen by the world health organization (WHO) . Patients with gastric precancerous lesions that do not to be reversed are considered to be at high risk for gastric cancer development. Therefore, effective remedies for H. pylori-induced gastric mucosa inflammation should be improved to prevent gastric cancer development , and updated therapies are urgently needed to effectively suppress H. pylori- or H. pylori-induced gastric mucosa inflammation . At present, there have been many studies on the effects of H. pylori infection treated by traditional Chinese medicine (TCM) . The fifth Chinese national consensus report on H. pylori infection management has proposed that TCM and proprietary Chinese medicines were worthy to be validated for H. pylori treatment [7, 8]. TCM, for example Banxia Xiexin decoction, has been proved to be effective in reducing drug resistance and increasing H. pylori eradication rate .
Tibetan medicine has a long history of 3800 years spanning from the sixth century Anno Domini (A. D.) . Zuozhu-Daxi (ZZDX) is a classic traditional Tibetan medicine, which composing of Calcite Lactis Praeparata, Calciosinti, Bambusae Concretio Silicea, Herba Aconiti Tangutici, Croci Stigma, Myristicae Semen, Tsaoko Fructus, Carthami Flos, Pulvis Fellis Ursi, Artificial Bovis Calculus, Artificial Moschus, etc., as shown in Table 1. ZZDX, possessing the efficacy of calming the liver, invigorating the stomach, clearing heat, curing anabrosis and relieving swellness , has a more than 600-year history of practical application. In Tibetan hospitals, ZZDX has been used for the treatment of liver pain, indigestion, “Huangshui” disease, visceral tumors, and food poisoning. Particularly, it has been widely used for digestive diseases, such as gastrohelcosis, duodenal ulcer, chronic gastritis, and gastric cancer . In the current study, we elucidated the effects and potential mechanisms of ZZDX on gastric mucosa inflammation in vivo and in vitro using H. pylori infected mice and gastric epithelial cell lines.
Materials and methods
ZZDX was provided by Tibet Ganlu Tibetan Medicine Co., Ltd., and its detailed information is shown in Table 1. After grinding, ZZDX was suspended in phosphate-buffered saline (PBS) to appropriate concentration for in vivo and in vitro experiments.
H. pylori culture
H. pylori strains ATCC 26,695 and SS1 were obtained from the Key Laboratory for Helicobacter pylori Infection and Upper Gastrointestinal Diseases in Peking University Third Hospital, and the strains ATCC 26,695 and SS1 were cultured on blood agar plates containing 39 g/L Columbia solid culture medium (Oxoid), 5% (v/v) sheep’s blood (Curtin Matheson, Jessup, MD, USA) supplemented with antibiotics amphotericin B (4 μg/mL) (Life Tech), trimethoprim (4 μg/mL) and vancomycin (4 μg/mL). The plates were incubated in a microaerobic environment [5% (v/v) O2, 10% (v/v) CO2 and 85% (v/v) N2] at 37 °C. H. pylori were harvested directly from 24- to 48-h plate cultures. H. pylori strains were examined before harvesting to be confirmed through Gram staining, urease tests, oxidase tests and catalase tests.
H. pylori-infected animal models and ZZDX treatment
A total of twenty-four six-week-old male specific pathogen free (SPF) level C57BL/6 mice were purchased from the China National Institute for Food and Drug Control (Daxing) Animal Resource Center and kept in an air-conditioned and barrier environment. These twenty-four mice were divided into four groups. Group 1 was the negative control (NC) group, which was intubated with Brucella broth alone. Group 2 was the H. pylori-infected (HP) group, and every mouse was intubated five times with 0.5 ml Brucella broth of H. pylori SS1 containing 3 × 108 CFU/mL. Group 3 was the low-dose ZZDX-treated (HP + ZZDX low-dose) group, with 0.083 g/kg ZZDX treatment for seven days after H. pylori infection. Group 4 was the high-dose ZZDX-treated group (HP + ZZDX high-dose), with 0.166 g/kg ZZDX treatment for seven days after H. pylori infection. Subsequently, the mice were killed by cervical dislocation. Blood and gastric tissues were processed and collected for further analyses.
The reasoning for our choice of ZZDX dose was based on the clinical dose of ZZDX. In clinical practice, the recommended daily dose of ZZDX was 1000 mg per person (60 kg weight), i.e., 8.3 mg/kg every day. According to the body surface area method in pharmacology, the dose used in mice should be approximately ten times the dose used in humans. Therefore, the daily dose of ZZDX in mouse models should be 83 mg/kg. In this study, two doses, 0.083 g/kg/day and 0.166 g/kg/day, were investigated.
The dissected gastric tissues along the greater curvature were washed with PBS, fixed in paraformaldehyde, embedded in paraffin, and sliced into 3 μm sections. Each specimen was stained by hematoxylin–eosin (HE) to evaluate the pathology of gastric mucosa inflammation under microscopy. Moreover, immunohistochemical (IHC) testing was used to evaluate the infection status of H. pylori (H. pylori Antibody Reagent for Immunohistochemistry, ZSGB-BIO, Beijing, China) and the expression levels of proteins. The expression levels of ACOT1 and ELOVL4 (polyclonal rabbit anti-human antibodies at a concentration of 1:1000, ImmunoWay Biotechnology Company, Texas, USA) were detected by IHC testing following the manufacturer’s instructions. Histopathological analysis was performed independently by two experienced pathologists.
Reactive oxygen species (ROS) measurement
ROS levels in serum were evaluated using a detection kit (BBoxiProbe O12 ROS, BestBio, Shanghai, China). Briefly, 10 μL of O12 probe diluted tenfold in ddH2O was added to 100 μL fresh serum and incubated at 37 ℃ for 30 min in the dark. The fluorescence intensity was detected at an excitation wavelength of 488 nm and an emission wavelength of 530 nm.
IL-1α, IL-6, and PGE2 expression levels in animal serum and cell culture supernatant were measured using an ELISA kit (MLBio, Shanghai, China) following the manufacturer’s instructions.
RNA extraction and real-time PCR analysis
Total RNA from tissue and cells was extracted using TRIzol (Invitrogen, Shanghai, China). RNA was reverse-transcribed into cDNA using the Super-Script First-Strand cDNA System (Invitrogen, Carlsbad, CA, USA), and real-time qPCR monitoring of cDNA was performed using the Roche LightCycler 480 sequence detection system (Roche, Mannheim, USA). Beta-actin (Actb) was used as an internal reference gene, and the primers used for RT-qPCR are shown in Table 2 below.
RNA sequencing for mouse gastric tissue
Total RNA was extracted from mouse gastric tissue using TRIzol according to the manufacturer's protocol. The RNA quality was checked by a Bioanalyzer 2100 (Agilent, USA), and the integrity number (RIN) of all the RNA samples was > 9.0.
The sequencing libraries were prepared using the Illumina TruSeqTM RNA Sample Prep Kit. Briefly, poly-A-containing mRNA was isolated from the total RNA by poly-T oligo-attached magnetic beads. cDNA was synthesized using random primers through reverse transcription. After ligation with the adaptor, the cDNA was amplified by 15 cycles of PCR, and then 200-bp fragments were isolated using gel electrophoresis. Finally, the products were sequenced by an Illumina NovaSeq 6000 instrument at Majorbio Co., Ltd. (China). The raw data have been submitted to the NCBI Gene Expression Omnibus (GEO) database under accession number GSE.
After sequencing, the screening of DEGs was based on their TPM (transcripts per kilobase million) values. A false discovery rate (FDR) of 0.05 and an absolute value of log2FC > 1 were used to identify significant DEGs. To inspect the functions of DEGs, GO enrichment analysis and KEGG pathway enrichment analysis of the DEGs were performed.
Cell culture, co-culture assays and ZZDX treatment
Human gastric epithelial GES-1 cells were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium supplemented with 10% (v/v) fetal bovine serum (FBS) (PAN-Biotech, Adenbach, Germany) at 37 °C in a humidified incubator at 5% (v/v) CO2. For co-culturing of cells and strains, first, H. pylori 26,695 were harvested from 24- to 48-h plate cultures, washed with PBS three times, and resuspended in cell growth medium and diluted to a final concentration of 1 × 108 CFU/mL. Then, GES-1 cells were plated one day before H. pylori treatment and rinsed once with PBS before fresh growth medium was added. Finally, the diluted bacterial strains were added to the cell medium at multiplicities of infection (MOIs) of 100:1. Zuozhu-Daxi was added to the co-cultured cells at concentrations of 20 μg/mL, 50 μg/mL, 100 μg/mL and 200 μg/mL. Uninfected GES-1 cells were negative controls. Cells co-cultured only with H. pylori were positive controls.
Western blot analysis
Proteins related to the PPAR signalling pathway were detected by Western blot analysis. Harvested cells were lysed in cell lysis buffer containing protease inhibitors for 30 min on ice. Then, the cell lysate was centrifuged at 15 000 × g at 4 °C for 10 min, and the supernatant was collected. The total protein concentration was measured by a bicinchoninic acid (BCA) protein assay kit (Thermo Scientific, Shanghai, China). 10% (w/v) SDS-PAGE was used to separate proteins, and then electrophoretically transferred proteins onto PVDF membranes. The membranes were blocked in 5% (w/v) fat-free milk in PBS supplemented with 0.1% (v/v) Tween-20 at room temperature for 1 h. After blocking, the membranes with proteins were incubated overnight at 4 °C with antibodies against ELOVL4 (polyclonal rabbit anti-human antibody, Proteintech, Rosemont, USA), ACOT1 (polyclonal rabbit anti-human antibody, Abcam, Shanghai, China), SCD1 (monoclonal rabbit anti-human antibody, Abcam, Shanghai, China), PPAR (polyclonal mouse anti-human antibody, ImmunoWay Biotechnology Company, Texas, USA) and β-actin (polyclonal rabbit anti-human antibody, CST, Shanghai, China). After being washed three times for 10 min each in PBS supplemented with 0.1% (v/v) Tween-20, the membranes were incubated with a secondary antibody for 1 h at room temperature. Then, the membranes were washed as in the previous step, and protein bands were scanned by an Odyssey Imager (LI-COR Biosciences).
Data were presented as the mean ± s.d. of three independent experiments. The differences among more than two groups were analysed using one-way ANOVA. The differences between two groups were analysed using Student’s t test. All statistical analyses were performed using SPSS 23.0 software. P values < 0.05 were considered statistically significant.
ZZDX treatment reversed the gastric mucosa injury induced by H. pylori but did not decrease H. pylori colonization in mouse gastric mucosa
HE staining was used to evaluate the pathology of gastric mucosa inflammation under microscopy. Our results showed that the H. pylori-infected gastric mucosa inflammation mouse model was successfully established. In Fig. 1, the gastric mucosa of the NC group was normal (Fig. 1a). In the HP group, the gastric mucosa was injured and showed erosion (Fig. 1b). After ZZDX treatment, the gastric mucosa injury caused by H. pylori infection could be reversed to a certain extent (Fig. 1c, d). To gain further insight into the status of H. pylori in gastric mucosa, we assayed H. pylori colonization in mouse gastric mucosa using H. pylori immunohistochemical staining, and the results showed that H. pylori was successfully colonized in the HP group (Fig. 2a, b). However, the colonization of H. pylori in mouse gastric mucosa was not decreased after ZZDX treatment (Fig. 2c, d).
ZZDX treatment decreased the expression levels of inflammatory factors induced by H. pylori infection
To examine whether ZZDX could decrease the expression levels of inflammatory factors induced by H. pylori infection, real-time PCR for gastric mucosa tissues and ELISA for serum were used to measure the levels of inflammatory factors. The real-time PCR results for gastric mucosa tissues showed that H. pylori infection could significantly increase the mRNA levels of IL-1α, IL-8 and NOD1 (P < 0.05), but no change was found for TNF-α. After ZZDX treatment at the high dose of 0.166 g/kg, the mRNA level of IL-1α in gastric mucosa was downregulated, with no significant difference (Fig. 3a), and the mRNA levels of IL-8 and NOD1 in gastric mucosa were downregulated significantly (Fig. 3b, c). The ELISA results showed that H. pylori infection significantly upregulated the levels of IL-1A, IL-6 and PGE2 in the serum of the mouse model (Fig. 4). After ZZDX treatment at either the low dose of 0.088 g/kg or the high dose of 0.166 g/kg, IL-1A and PGE2 were decreased in a dose-dependent manner (Fig. 4a, b), while IL-6 was reversed significantly at the high dose (Fig. 4c).
Exploring the anti-inflammatory mechanisms of ZZDX on H. pylori-infected gastric mucosa using RNA sequencing
To explore the potential anti-inflammatory molecular mechanisms of ZZDX on H. pylori-infected gastric mucosa, RNA sequencing was used to analyse the differentially expressed genes among groups, including 2 mice from the NC group, 2 mice from the HP group, and 3 mice from the ZZDX-treated groups. The expression levels of IL-8 in the NC group were 0.020 and 0.051, 0.391 and 0.534 in the HP group and 0.037, 0.136, and 0.024 in the ZZDX-treated group at the high dose of 0.166 g/kg. The histopathology of the mucosa in the above three groups was normal, chronic gastritis and normal, respectively. A heatmap was constructed from the data obtained for the differentially expressed genes (Fig. 5a). Between the NC group and the HP group, 2596 genes were identified to be differentially expressed significantly. Between HP groups with or without ZZDX treatment, 401 genes were identified to be differentially expressed significantly, including 119 downregulated genes and 282 upregulated genes. A volcano map was constructed from the differentially expressed genes between the HP groups with or without ZZDX treatment (Fig. 5b). Gene Ontology (GO) enrichment of differentially expressed genes was performed, and the top 20 enriched GO terms were shown in Fig. 5c according to the P values of the enriched GO terms. The top four most enriched GO terms were “positive regulation of cell differentiation”, “regulation of cell development”, “regulation of nervous system development”, and “positive regulation of nervous system development”. KEGG pathway analysis of genes regulated by ZZDX treatment was shown in Fig. 5d, indicating that the differentially expressed genes regulated by ZZDX were most enriched in “Biosynthesis of unsaturated fatty acids”, “Fatty acid elongation”, “Fatty acid metabolism”, and “Circadian entrainment”. Genes such as acyl-CoA thioesterase 1 (ACOT1), ELOngation of Very Long-chain fatty acid-4 (ELOVL4), stearoyl-CoA desaturase 1 (SCD1) and peroxisome proliferator activated receptor gamma (PPARG) were included in the prominent pathway “biosynthesis of unsaturated fatty acids”, and their expression levels were significantly affected by H. pylori infection and drug administration (Fig. 6a).
Verification of four identified proteins
In support of the above results, RT-qPCR and western blot analysis were conducted to monitor changes in the levels of four identified genes implicated in “biosynthesis of unsaturated fatty acids” (Fig. 6b–d). As shown in the results, the expression levels of ELOVL4, ACOT1 and SCD1 increased when H. pylori was infected and decreased after ZZDX treatment. The IHC staining results of mouse gastric mucosa also showed that the expression levels of ELOVL4 and ACTO1 were upregulated in situ after H. pylori infection and significantly decreased after ZZDX treatment (Fig. 6e, f).
Furthermore, the above results were verified in vitro. H. pylori infection significantly increased the mRNA levels of IL-6 and IL-8, and the mRNA level of IL-1 was also increased. After ZZDX treatment, the mRNA levels of IL-1 and IL-6 were downregulated significantly (Fig. 7a). The expression levels of ELOVL4, SCD1 and ACOT1 before and after ZZDX treatment were further verified by RT-qPCR and western blot, which were consistent with the results above (Fig. 7b, c). These results suggested that ZZDX can effectively inhibit the increase in lipid metabolism and inflammation caused by H. pylori infection, thereby effectively alleviating the occurrence and development of gastritis and gastric mucosal diseases caused by H. pylori infection.
It is estimated that more than half of the world’s population are infected with H. pylori . As a class I carcinogen by the WHO, the carcinogenesis induced by H. pylori from chronic gastritis to ultimately gastric cancer is a multi-step and multi-level process [13, 14]. To reduce the incidence of gastric cancer, eradication of H. pylori is the main therapeutic strategy by the combination of antibiotics and proton pump inhibitors. However, it poses a huge challenge to the eradication therapy of H. pylori owing to undesired side effects as well as the emergence of steadily increasing antibiotic-resistant strains .
In recent years, traditional medicine has become a source of new pharmaceuticals due to their strong efficacy with fewer side effects and lower toxicity, and have made surprising progress in the treatment of various diseases, such as tumors, inflammation, gout, atherosclerosis, virus infection, bacterial infection and fungal infection [16,17,18,19,20,21,22]. Tibetan medicine, as an important traditional medicine, has unique advantages in the treatment of peptic ulcers. Of which, ZZDX is mainly applied for the treatment of chronic gastritis, peptic ulcer and gastric cancer, and shows a potential reversal effect on gastric mucosal damage [23, 24].
In this study, mice were orally treated with ZZDX to rescue gastric mucosa inflammation induced by H. pylori infection, and the infection status of H. pylori was also measured in the mouse gastric mucosa. The results showed that ZZDX might have a reversal effect on the inflammation of gastric mucosa induced by H. pylori infection. According to the literature reports, IL-1α , IL-8 , TNF-α , and NOD1  play an important role in the H. pylori bacterial infection process and gastric mucosal inflammation and promote the synthesis and release of other cytokines. After H. pylori infection, the immune system can be activated. This could induce the production of inflammatory cytokines and activation of neutrophils and monocytes, accompanied by active free radical production, such as nitric oxide (NO), which will lead to gastric epithelial cell mutation and consequently result in inflammatory injury . In the present study, ZZDX was found to significantly decrease the mRNA levels of IL-8 and NOD1 in gastric mucosa and downregulate the IL-1A, PGE2 and IL-6 levels in mouse serum, indicating that inflammation was significantly reversed . Moreover, the PGE2 pathway plays a pivotal role in inflammation-induced gastric tumorigenesis , thus ZZDX might be able to inhibit the pathway of gastric tumorigenesis.
Subsequently, the mechanisms of reversing gastric mucosa inflammation were further explored using RNA sequencing and then verified in vivo and in vitro. According to the results of RNA sequencing, ZZDX could affect the pathways of unsaturated fatty acids biosynthesis, fatty acid elongation, and fatty acid metabolism. These pathways have been reported to be associated with ROS formation and can induce inflammation [32, 33]. The levels of ELOVL4, ACOT1 and SCD1 were significantly decreased after ZZDX treatment. These molecules are involved in the unsaturated fatty acid biosynthetic process [34,35,36]. ELOVL4, homologous to the ELO family which take part in fatty acid metabolism , has been reported in a gene metabolic signature, which is considered to be correlated with the overall survival (OS) and tumor immune microenvironment (TIME) in gastric cancer . ACOT1, a gene for intracellular energy metabolism, could significantly promote the formation of gastric cancer tumor tissues and is associated with poor prognosis of gastric cancer . SCD1, an enzymatic node which can convert saturated fatty acids into monounsaturated fatty acids, can promote the tumorigenesis of multiple cancers and has been considered to be a therapeutic target for some cancers . In gastric cancer, SCD1 has been found to facilitate tumor growth and predict poor prognosis . ZZDX treatment might rescue the progress of H. pylori-induced diseases by inhibiting these genes-associated molecular pathways in the pathogenic mechanisms.
However, we did not find a decrease in H. pylori infection status after treatment with ZZDX alone. Some previous studies have showed that ZZDX together with other medicines could be effective for H. pylori eradication. The eradication rate for H. pylori was found to be 77.8%  of ZZDX, together with Tibetan medicines such as Wuwei Shiliuwan, Ershiyiwei Hanshuishiwan, and Shiwuwei Heiyaowan. In addition, ZZDX with triple therapy of omeprazole, amoxicillin and clarithromycin could quickly improve clinical symptoms and effectively reduce the level of inflammatory indicators , and ZZDX with triple therapy of rebeprazole, amoxicillin and clarithromycin was more effective for the treatment of H. pylori-associated peptic ulcers in symptom relief rate and H. pylori eradication rate than those of conventional triple therapy . Further studies should be performed to certify the potential clinical application of ZZDX together with other drugs in relieving symptoms and H. pylori eradication.
ZZDX is a complicated prescription composed of 35 mineral or animal or plant medicinal materials. Its chemical constituents are extremely complex, and it is really a tough work to identify its anti-inflammatory constituents. Activity guided chemical investigation is necessary to clarify the bioactive substance in the future researches. Here, the possible major bioactive constituents contributing to the preventive efficacy on H. pylori-induced inflammation of ZZDX are proposed through analysis of the prescription compositions and literatures. Calcite Lactis Praeparata, with calcium sulfate as the main constituent and accounting for about 15% of the total prescription amount of ZZDX, has been widely used for the treatment of gastric cancer and gastritis  and might be regarded as the main active component. Moreover, the characteristic anti-inflammatory constituents of cholanic acids (such as cholic acid, deoxycholic acid, ursodeoxycholic acid) [45, 46] and cycloketones (such as muscone)  in the animal medicines of Pulvis Fellis Ursi, Bovis Calculus (artificial) and Moschus (artificial), should play a key role in the rescue of H. pylori-induced inflammation. In addition, various anti-inflammatory constituents in the herbal medicines of ZZDX, such as sesquiterpene lactones in Aucklandia lappa Decne.  and Inula racemose Hook. f. , alkaloids in Aconitum naviculare (Bruhl.) Stapf , iridoid glycosides and phenylethanol glycosides in Veronica eriogyne H. Winkl. , organic acids in Terminalia chebula Retz. , and flavonoids in Taraxacum officinale F. H. Wigg . and other herbs, might also be the important bioactive constituents that contributed to the gastric mucosa inflammation reversal.
It has been a field of current interest that diverse traditional medicines are evaluated for application against H. pylori. Many TCMs, such as turmeric, propolis, and garlic, have been reported to have anti-inflammatory, antioxidant, and antibacterial effects against H. pylori [53,54,55,56]. The anti-inflammatory and antioxidant effects of these medicines are mainly reflected in the inhibition of proinflammatory factors and reactive oxygen species generated by the interaction of H. pylori with gastric mucosa cells . The antibacterial effects of TCMs against H. pylori have also been studied. On the one hand, these medicines can inhibit H. pylori enzymes such as urease, which decreases the acidity of gastric juice. On the other hand, they can inhibit the adhesion of H. pylori to gastric mucosa . In addition, some TCMs that play an antibacterial role by targeting biofilms, proteins of the primary metabolism and virulence factors of H. pylori, have received more attention .
In view of that, it is suggested that TCM therapy cannot be used as monotherapy, although it has great potential to assist treatment [59, 60]. Furthermore, although there are many studies of TCM against H. pylori in vitro models, reliable randomized and controlled clinical trials which compare the efficacy of recommended triple therapies with herbal medicine on H. pylori treatment are still lacking . Many factors must be taken into consideration, such as the identification, extraction and preparation of effective antibacterial components in herbal medicine, dose, formulation, dosing frequency, and duration of treatment. What needs to be illustrated is that some results of mechanistic exploration in this study showed obvious variation tendencies instead of significant changes, which might be due to the insufficient numbers of mice. This is a pilot study heralding the clinicopathological significance and mechanisms of ZZDX in H. pylori infection and provide clues for future studies.
Availability of data and materials
The authors hereby declare that the data and materials in this study will be presented upon request from the corresponding author.
Acyl-CoA thioesterase 1
- A. D:
ELOngation of Very Long-chain fatty acid-4
- H. pylori:
Multiplicities of infection
Peroxisome proliferator activated receptor gamma
Real-time quantitative PCR
Reactive oxygen species
Specific pathogen free
Stearoyl-CoA desaturase 1
Tumor immune microenvironment
World health organization
Hooi JKY, Lai WY, Ng WK, et al. Global prevalence of helicobacter pylori infection: systematic review and meta-analysis. Gastroenterology. 2017;153(2):420–9.
Jessurun J. Helicobacter pylori: an evolutionary perspective. Histopathology. 2021;78(1):39–47.
Navashenaq JG, Shabgah AG, Banach M, et al. The interaction of helicobacter pylori with cancer immunomodulatory stromal cells: New insight into gastric cancer pathogenesis. Semin Cancer Biol. 2021;86(Pt 3):951–9.
Watari J, Chen N, Amenta PS, et al. Helicobacter pylori associated chronic gastritis, clinical syndromes, precancerous lesions, and pathogenesis of gastric cancer development. World J Gastroenterol. 2014;20(18):5461–73.
Savoldi A, Carrara E, Graham DY, Conti M, Tacconelli E. Prevalence of antibiotic resistance in helicobacter pylori: a systematic review and meta-analysis in world health organization regions. Gastroenterology. 2018;155(5):1372-1382.e1317.
Li Y, Li X, Tan Z. An overview of traditional Chinese medicine therapy for Helicobacter pylori-related gastritis. Helicobacter. 2021;26(3): e12799.
Liu WZ, Xie Y, Lu H, et al. Fifth Chinese national consensus report on the management of helicobacter pylori infection. Helicobacter. 2018;23(2): e12475.
Li L, Meng F, Zhu S, et al. Efficacy and safety of Wei Bi Mei, a Chinese herb compound, as an alternative to bismuth for eradication of helicobacter pylori. Evid Based Complement Alternat Med. 2018;2018:4320219.
Li RJ, Dai YY, Qin C, et al. Application of traditional Chinese medicine in treatment of Helicobacter pylori infection. World J Clin Cases. 2021;9(35):10781–91.
Zuskin E, Lipozencić J, Pucarin-Cvetković J, et al. Ancient medicine–a review. Acta Dermatovenerol Croat. 2008;16(3):149–57.
Hai J. Effect of western medicine triple combination combined with Tibetan medicine Zuozhu-Daxi pill on improving gastrointestinal function and serum CRP and IL-4 levels in the treatment of peptic ulcer. Chin J Ethnic Med. 2022;28(2):7–8.
Hu W. Clinical observation on the treatment of digestive tract tumor vomiting after chemotherapy with Zuozhu-Daxi combined with Astragalus injection and Xiaobanxia pill. Jilin Medical J. 2011;32(8):1500–1.
Baj J, Korona-Glowniak I, Forma A, et al. Mechanisms of the epithelial-mesenchymal transition and tumor microenvironment in helicobacter pylori-induced gastric cancer. Cells. 2020;9(4):1055.
Camilo V, Sugiyama T, Touati E. Pathogenesis of Helicobacter pylori infection. Helicobacter. 2017;22(Suppl):1.
Cardos IA, Zaha DC, Sindhu RK, Cavalu S. Revisiting therapeutic strategies for H. pylori treatment in the context of antibiotic resistance focus on alternative and complementary therapies. Molecules. 2021;26(19):6078.
Varghese R, Dalvi YB. Natural products as anticancer agents. Curr Drug Targets. 2021;22(11):1272–87.
Winand L, Sester A, Nett M. Bioengineering of anti-inflammatory natural products. ChemMedChem. 2021;16(5):767–76.
El-Tantawy WH. Natural products for the management of hyperuricaemia and gout: a review. Arch Physiol Biochem. 2021;127(1):61–72.
Zhang S, Li L, Chen W, Xu S, Feng X, Zhang L. Natural products: the role and mechanism in low-density lipoprotein oxidation and atherosclerosis. Phytother Res. 2021;35(6):2945–67.
Boozari M, Hosseinzadeh H. Natural products for COVID-19 prevention and treatment regarding to previous coronavirus infections and novel studies. Phytother Res. 2021;35(2):864–76.
Sadeer NB, Mahomoodally MF. Antibiotic potentiation of natural products: a promising target to fight pathogenic bacteria. Curr Drug Targets. 2021;22(5):555–72.
Yuan S, Gopal JV, Ren S, Chen L, Liu L, Gao Z. Anticancer fungal natural products: mechanisms of action and biosynthesis. Eur J Med Chem. 2020;202: 112502.
Wang H. Talk shallowly that on the clinical application of Tibetan medicine Zuozhu Daxi. Chin J Ethnomed and Ethnopharm. 2014;23:4–5.
Shen F, Li X, Qi D, Jiang H, Guo Z, Chen P. Relationship between the genotypes of Helicobacter pylori in fection and gastroin testinal diseases. Chin J Nosocomiology. 2022;32(3):417–21.
Bertheloot D, Latz E. HMGB1, IL-1α, IL-33 and S100 proteins: dual-function alarmins. Cell Mol Immunol. 2017;14(1):43–64.
Zeng B, Chen C, Yi Q, et al. N-terminal region of Helicobacter pylori CagA induces IL-8 production in gastric epithelial cells via the β1 integrin receptor. J Med Microbiol. 2020;69(3):457–64.
Suganuma M, Watanabe T, Sueoka E, Lim IK, Fujiki H. Role of TNF-α-inducing protein secreted by helicobacter pylori as a tumor promoter in gastric cancer and emerging preventive strategies. Toxins. 2021;13(3):181.
Suarez G, Romero-Gallo J, Piazuelo MB, et al. Nod1 imprints inflammatory and carcinogenic responses toward the gastric pathogen helicobacter pylori. Cancer Res. 2019;79(7):1600–11.
Figueiredo CA, Marques CR, Costa Rdos S, da Silva HB, Alcantara-Neves NM. Cytokines, cytokine gene polymorphisms and Helicobacter pylori infection: friend or foe? World J Gastroenterol. 2014;20(18):5235–43.
Chen Y, Wang X, Yu Y, et al. Serum exosomes of chronic gastritis patients infected with Helicobacter pylori mediate IL-1α expression via IL-6 trans-signalling in gastric epithelial cells. Clin Exp Immunol. 2018;194(3):339–49.
Cao D, Jiang J, Tsukamoto T, et al. Canolol inhibits gastric tumors initiation and progression through COX-2/PGE2 pathway in K19–C2mE transgenic mice. PLoS ONE. 2015;10(3): e0120938.
Gehrmann W, Würdemann W, Plötz T, Jörns A, Lenzen S, Elsner M. Antagonism between saturated and unsaturated fatty acids in ROS mediated lipotoxicity in rat insulin-producing cells. Cell Physiol Biochem. 2015;36(3):852–65.
Trommer S, Leimert A, Bucher M, Schumann J. Polyunsaturated fatty acids induce ROS synthesis in microvascular endothelial cells. Adv Exp Med Biol. 2018;1072:393–7.
Sun P, Zhou Q, Monroig Ó, et al. Cloning and functional characterization of an elovl4-like gene involved in the biosynthesis of long-chain polyunsaturated fatty acids in the swimming crab Portunus trituberculatus. Comp Biochem Physiol B Biochem Mol Biol. 2020;242: 110408.
Duan S, Zhang M, Li J, et al. Uterine metabolic disorder induced by silica nanoparticles: biodistribution and bioactivity revealed by labeling with FITC. J Nanobiotechnology. 2021;19(1):62.
Li Z, Lu S, Cui K, et al. Fatty acid biosynthesis and transcriptional regulation of Stearoyl-CoA Desaturase 1 (SCD1) in buffalo milk. BMC Genet. 2020;21(1):23.
Vasireddy V, Sharon M, Salem N Jr, Ayyagari R. Role of ELOVL4 in fatty acid metabolism. Adv Exp Med Biol. 2008;613:283–90.
Yang Y, Chen Z, Zhou L, et al. In silico development and validation of a novel glucose and lipid metabolism-related gene signature in gastric cancer. Transl Cancer Res. 2022;11(7):1977–93.
Wang F, Wu J, Qiu Z, et al. ACOT1 expression is associated with poor prognosis in gastric adenocarcinoma. Hum Pathol. 2018;77:35–44.
Raeisi M, Hassanbeigi L, Khalili F, Kharrati-Shishavan H, Yousefi M, Mehdizadeh A. Stearoyl-CoA desaturase 1 as a therapeutic target for cancer: a focus on hepatocellular carcinoma. Mol Biol Rep. 2022;49(9):8871–82.
Wang C, Shi M, Ji J, et al. Stearoyl-CoA desaturase 1 (SCD1) facilitates the growth and anti-ferroptosis of gastric cancer cells and predicts poor prognosis of gastric cancer. Aging. 2020;12(15):15374–91.
Huang F, Ren W, Yang G. Clinical observation on therapeutic efficiency of tibean medicine used in treating atrophic gastritis. Chin J of Ethnic Med. 2000;6(1):10–2.
Yu G, Tan Y. Clinical observation of combined treatment of Helicobacter pylori positive peptic ulcer with Zuozhu-Daxi. Chin J Adv Med Educ. 2012;35(z2):61–2.
Hu M, Zhou H, Wang M, Chen C, Du Y. Recent development of study on mongolian medicine gypsum fibrosum. J Med Pharm of Chin Mnorities. 2014;20(9):34–6.
Li H, Wang Q, Chen P, Zhou C, Zhang X, Chen L. Ursodeoxycholic acid treatment restores gut microbiota and alleviates liver inflammation in non-alcoholic steatohepatitic mouse model. Front Pharmacol. 2021;12: 788558.
Chen X, Mellon RD, Yang L, Dong H, Oppenheim JJ, Howard OM. Regulatory effects of deoxycholic acid, a component of the anti-inflammatory traditional Chinese medicine Niuhuang, on human leukocyte response to chemoattractants. Biochem Pharmacol. 2002;63(3):533–41.
Yu S, Zhao G, Han F, et al. Muscone relieves inflammatory pain by inhibiting microglial activation-mediated inflammatory response via abrogation of the NOX4/JAK2-STAT3 pathway and NLRP3 inflammasome. Int Immunopharmacol. 2020;82: 106355.
Chun J, Choi RJ, Khan S, et al. Alantolactone suppresses inducible nitric oxide synthase and cyclooxygenase-2 expression by down-regulating NF-κB, MAPK and AP-1 via the MyD88 signaling pathway in LPS-activated RAW 264.7 cells. Int Immunopharmacol. 2012;14(4):375–83.
Luo M, Li C, Lin L, Wang Z, Guo W. Research progress on tibetan medicinal herb ponkar. Chin J Exp Tradit Med Formulae. 2012;18(12):298–302.
Du Y, Wang X, Yang M. Advances in pharmacological activities of the medicinal plants of genus Veronica. Chin Med J Res Prac. 2013;27(06):77–80.
Cai L, Wei Z, Zhao X, Li Y, Li X, Jiang X. Gallic acid mitigates LPS-induced inflammatory response via suppressing NF-κB signalling pathway in IPEC-J2 cells. J Anim Physiol Anim Nutr (Berl). 2022;106(5):1000–8.
Schütz K, Carle R, Schieber A. Taraxacum–a review on its phytochemical and pharmacological profile. J Ethnopharmacol. 2006;107(3):313–23.
Shetty NP, Prabhakaran M, Srivastava AK. Pleiotropic nature of curcumin in targeting multiple apoptotic-mediated factors and related strategies to treat gastric cancer: a review. Phytother Res. 2021;35(10):5397–416.
Alaribe CS, Esposito T, Sansone F, et al. Nigerian propolis: chemical composition, antioxidant activity and alpha-amylase and alpha-glucosidase inhibition. Nat Prod Res. 2021;35(18):3095–9.
Korona-Glowniak I, Glowniak-Lipa A, Ludwiczuk A, Baj T, Malm A. The in vitro activity of essential oils against helicobacter pylori growth and urease activity. Molecules. 2020;25(3):586.
Ullah H, Di Minno A, Santarcangelo C, et al. Vegetable extracts and nutrients useful in the recovery from helicobacter pylori infection: a systematic review on clinical trials. Molecules. 2021;26(8):2272.
Wang LS, Echeveste CE, Yu J, et al. Can natural products suppress resistant helicobacter pylori to fight against gastric diseases in humans. eFood. 2020;1(1):53–60.
Roszczenko-Jasinska P, Wojtys MI, Jagusztyn-Krynicka EK. Helicobacter pylori treatment in the post-antibiotics era-searching for new drug targets. Appl Microbiol Biotechnol. 2020;104(23):9891–905.
Lin J, Huang WW. A systematic review of treating Helicobacter pylori infection with traditional Chinese medicine. World J Gastroenterol. 2009;15(37):4715–9.
Hu Q, Peng Z, Li L, et al. The efficacy of berberine-containing quadruple therapy on helicobacter pylori eradication in china: a systematic review and meta-analysis of randomized clinical trials. Front Pharmacol. 2019;10:1694.
This study was funded by the Tibet Autonomous Region Administration of Traditional Tibetan Medicine (Grant No. JJKT2020014), National Natural Science Foundation of China (Grant No. 81700496), and Key Laboratory for Helicobacter pylori Infection and Upper Gastrointestinal Diseases, Beijing Key Laboratory (No. BZ0371).
Ethics approval and consent to participate
The study was approved by Peking University Biomedical Ethics Committee, Laboratory Animal Welfare Ethics Branch (Ethics approval number for the use of animals in this study was LA2019343).
Consent for publishlication
We declare that the Publisher has the authors’ permission to publish the relevant contribution.
The authors declare no competing interest.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
About this article
Cite this article
Shi, Y., Ning, J., Norbu, K. et al. The tibetan medicine Zuozhu-Daxi can prevent Helicobacter pylori induced-gastric mucosa inflammation by inhibiting lipid metabolism. Chin Med 17, 126 (2022). https://doi.org/10.1186/s13020-022-00682-9
- Tibetan medicine
- Helicobacter pylori
- Gastric mucosal injury
- Gastric mucosal inflammation