ABSTRACT
BACKGROUND: Panax notoginseng (Burk.) F. H. Chen (PN) belonging to the genus Panax of family Araliaceae is widely used in traditional Chinese medicine to treat various diseases. PN taproot, as the most vital organ for the accumulation of bioactive components, presents a variable morphology (oval or long), even within the same environment. However, no related studies have yet explained the molecular mechanism of phenotypic differences. To investigate the cause of differences in the taproot phenotype, de novo and comparative transcriptomic analysis on PN taproot was performed. RESULTS: A total of 133,730,886 and 114,761,595 paired-end clean reads were obtained based on high-throughput sequencing from oval and long taproot samples, respectively. 121,955 unigenes with contig N50 = 1,774 bp were generated by using the de novo assembly transcriptome, 63,133 annotations were obtained with the BLAST. And then, 42 genes belong to class III peroxidase (PRX) gene family, 8 genes belong to L-Ascorbate peroxidase (APX) gene family, and 55 genes belong to a series of mitogen-activated protein kinase (MAPK) gene family were identified based on integrated annotation results. Differentially expressed genes analysis indicated substantial up-regulation of PnAPX3 and PnPRX45, which are related to reactive oxygen species metabolism, and the PnMPK3 gene, which is related to cell proliferation and plant root development, in long taproots compared with that in oval taproots. Furthermore, the determination results of real-time quantitative PCR, enzyme activity, and H2O2 content verified transcriptomic analysis results. CONCLUSION: These results collectively demonstrate that reactive oxygen species (ROS) metabolism and the PnMPK3 gene may play vital roles in regulating the taproot phenotype of PN. This study provides further insights into the genetic mechanisms of phenotypic differences in other species of the genus Panax.
Subject(s)
Panax notoginseng , Gene Expression Profiling , Hydrogen Peroxide , Panax notoginseng/genetics , Plant Roots/genetics , TranscriptomeABSTRACT
This work explored the feasibility of using biological polysaccharide to fabricate dissolvable microneedles (MNs) for the purpose of transdermal drug delivery and skin dendritic cell (DC) activation. Panax notoginseng polysaccharide (PNPS), a naturally derived immunoactive macromolecule, was used to fabricate dissolvable MNs. The prepared PNPS MNs showed a satisfactory mechanical strength and a skin penetration depth. By Franz diffusion cell assay, the PNPS MNs demonstrated a high transdermal delivery amount of model drugs. Furthermore, with the assistance of MNs, PNPS easily penetrated across the stratum corneum and target ear skin DCs, activating the maturation and migration of immunocytes by increasing the expressions of CD40, CD80, CD86, and MHC II of skin DCs. Consequently, the matured DCs migrated to the auricular draining lymph nodes and increased the proportions of CD4+ T and CD8+ T cells. Thus, PNPS might be a promising biomaterial for transdermal drug delivery, with adjuvant potential.
Subject(s)
Langerhans Cells/drug effects , Needles , Panax notoginseng/chemistry , Polysaccharides/chemistry , Administration, Cutaneous , Animals , B7-1 Antigen/metabolism , B7-2 Antigen/metabolism , CD40 Antigens/metabolism , Compressive Strength , Doxorubicin/administration & dosage , Fluorescein/administration & dosage , Fluorouracil/administration & dosage , Langerhans Cells/metabolism , Male , Mice , Myosin Heavy Chains/metabolism , Rats, Sprague-Dawley , Skin/cytology , Skin/drug effects , Skin/metabolism , SolubilityABSTRACT
In the current study, we developed a synergistic chemo-immunotherapy using doxorubicin (Dox) and a natural polysaccharide as immunomodulator. First, we isolated a polysaccharide (MPW) from the root of Lepidium meyenii Walp. (maca) and characterized its chemical properties. MPW contains â 4) -α-D-Glcp- (1 â glycosidic bonds, while the terminal α-D-Glcp- (1 â group is connected to the main chain through an O-6 bond. This polysaccharide was then modified by cationization (C-MPW) to enhance immunoregulatory activity. MPW and C-MPW were combined with Dox and their chemo-immunotherapy effects on 4T1 tumor-bearing mice were assessed. Results indicated that the combination of MPW/C-MPW exerted a stronger anti-tumor effect than Dox alone, while reducing systemic toxicity and inhibiting tumor metastasis. In addition, MPW and C-MPW exerted tumor immunotherapy effects through the NF-κB, STAT1, and STAT3 signaling pathways, redirecting TAMs to the M1 phenotype that facilitates immunological responses against tumors. As a result, the immunosuppressive tumor microenvironment was remodeled into an immune-activated state due to enhanced secretion of IL-12, TNF-α, and INF-γ. Moreover, C-MPW exerted a stronger immunomodulatory effect than MPW. In conclusion, MPW and its cationic derivative are promising tools for cancer immunotherapy.
Subject(s)
Breast Neoplasms/drug therapy , Dietary Carbohydrates/pharmacology , Immunologic Factors , Lepidium/chemistry , Plant Extracts/pharmacology , Polysaccharides/pharmacology , Tumor-Associated Macrophages/immunology , Animals , Apoptosis , Breast Neoplasms/immunology , Breast Neoplasms/metabolism , Breast Neoplasms/pathology , Cell Proliferation , Cytokines/metabolism , Female , Humans , Mice , Mice, Inbred BALB C , Mice, Nude , NF-kappa B/metabolism , Tumor Cells, Cultured , Tumor-Associated Macrophages/drug effects , Xenograft Model Antitumor AssaysABSTRACT
This study presented the first purification and characterization of a hepatoprotective polysaccharide (PNPS-0.5 M) from the residue of Panax notoginseng (Burk.) F.H. Chen. This polysaccharide included a backbone of (4 â 1)-linked GalA and branches of (1â)-linked Araf, (1â)-linked Rhap, and (5 â 1)-linked Araf and had an extremely high molecular weight (2600 kDa). We investigated the hepatoprotective effects of PNPS-0.5 M on mice with alcoholic liver damage (ALD). After administration of PNPS-0.5 M, the levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), triglyceride (TG), and hepatic malondialdehyde (MDA) were reduced to normal. In contrast, hepatic levels of alcohol dehydrogenase (ADH) and the antioxidant enzymes superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) were elevated to normal. Further investigations indicated that PNPS-0.5 M activated Nrf2 signaling as a protective mechanism against Cyp2e1 toxicity in ALD mice. Meanwhile, it strengthened the ADH pathway and suppressed the CAT pathway of alcohol metabolism to prevent peroxide accumulation, thereby ameliorating ALD. In the present study, we describe a novel acidic polysaccharide from P. notoginseng with hepatoprotective activity that facilitates the development and utilization of P. notoginseng resources.
Subject(s)
Liver Diseases, Alcoholic/drug therapy , Panax notoginseng/chemistry , Polysaccharides/therapeutic use , Protective Agents/therapeutic use , Animals , Biomarkers/metabolism , Cyclooxygenase 2/metabolism , Gene Expression Regulation/drug effects , Glycosides/chemistry , Hydrolysis , Liver/drug effects , Liver/pathology , Liver Diseases, Alcoholic/genetics , Male , Methylation , Mice , Monosaccharides/analysis , Polysaccharides/isolation & purification , Polysaccharides/pharmacology , Protective Agents/pharmacology , RNA, Messenger/genetics , RNA, Messenger/metabolism , Signal Transduction/drug effects , Spectroscopy, Fourier Transform Infrared , Uronic Acids/chemistryABSTRACT
Panax Notoginseng is a kind of herb material with high medicinal value, which requires adaptive planting environment, and not can be continuously cultivated in the same ground. Those reasons lead to a large number of low-grade Notoginseng appears in the market. The objective of this study is to discriminate adulterant of Notoginseng of different grades by FT-MIR spectroscopy couple with chemometrics. In the experiment, high-grade Notoginseng was adulterated with 14 blend ratios: 0%, 1%, 3%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, and 100% of low-grade Notoginseng. All samples were scanned in the range of 4000-400â¯cm-1 by FT-MIR spectra instrument in absorption mode. Baseline, standard normal variate (SNV), multiplicative scatter correction (MSC), orthogonal signal correction (OSC), first derivative (D1) with 11-points smoothing and second derivative (D2) with 11-points smoothing were used to preprocess the spectral data, in which Baseline combined with SNV and D1 with 11-points performed best. The spectral data in the range of 1485-405â¯cm-1 were selected by interval partial least squares (iPLS) for modeling. Then, Support vector machine (SVM) and linear discriminant analysis (LDA) were applied for modeling analysis. The best result was achieved by SVM, as the classification accuracy was 100%, which indicated that FT-MIR spectroscopy combined with chemometrics was an effective approach to identify Notoginseng powder adulteration. It could detect the blend ratio of 5% (w/w) as well as the blend ratio of over 5%.