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1.
Pharmaceutics ; 14(3)2022 Mar 03.
Article in English | MEDLINE | ID: mdl-35335934

ABSTRACT

Asthma, a common chronic pulmonary disorder characterized by airway remodeling, hyperresponsiveness and obstruction, can be aggravated by repeated exposure to particulate matter (PM). The potential effect and mechanisms of Asarum sieboldii Radix essential oil (AEO) against asthma were explored based on network pharmacology. AEO was pre-treated using a nebulizer for 3 weeks and the mice were sensitized to ovalbumin (OVA) and PM10 with the co-treatment of AEO for 4 weeks. In addition, A549 lung epithelial cells were sensitized with PM10 to investigate the underlying mechanisms of AEO regarding the lung-fibrosis-related mediators. The target genes of methyl eugenol, a main compound of AEO, were highly matched by 48% with the gene set of asthma. AEO markedly inhibited the increase in epithelial thickness through the accumulation of goblet cells in the airways. Collagen deposition in the lung tissues of OVA+PM10-challenged asthmatic mice was significantly decreased by AEO. AEO also inhibited the influx of inflammatory cells in the bronchoalveolar lavage fluid, as well as the increases in serum IgE and IgG2a and cytokines in the lung tissues. Furthermore, AEO regulated the expressions of fibrotic mediators, especially POSTN and TGF-ß. In conclusion, we expect that AEO can be one of the effective alternative therapeutics to relieve asthma.

2.
Article in English | MEDLINE | ID: mdl-33505503

ABSTRACT

Localized adiposity is not only a common aesthetic issue but also a health risk factor. Pharmacopuncture can be a therapeutic option for the imbalance of regional fat distribution. The tuber of Pinellia ternata has been prescribed as antitussive and expectorant as a traditional Korean medicine. This study investigated the effects of pharmacopuncture with P. ternata water extract (PT) on localized adiposity. Male C57BL/6J mice were fed on a high-fat diet (HFD) for 6 weeks. 100 µL of 10 mg/mL of PT was injected into the left-side inguinal fat pad, while saline was injected into the right-side inguinal fat pad as self-control. Treatments were performed 3 times per week for 4 weeks. The inguinal fat weight was analyzed by dual-energy X-ray absorptiometry. PT pharmacopuncture significantly decreased the weight of the inguinal fat pad. The adipocyte size was reduced with increases of lipolytic enzymes and lipophagy-related factors by PT pharmacopuncture. There was marked inhibition of lipid accumulation content in 3T3-L1 adipocytes by PT treatment. The expressions of adipose triglyceride lipase (ATGL), hormone-sensitive lipase (HSL), autophagy-related gene (ATG) 5, ATG7, and LC3 were markedly increased by PT treatments in vivo and in vitro. This study suggests that pharmacopuncture of Pinellia ternata has ameliorative effects on adiposity by lipid catabolic effects via activating both lipolysis and lipophagy in a localized region.

3.
Environ Toxicol Pharmacol ; 54: 169-176, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28743066

ABSTRACT

Juvenile sablefish, Anoplopoma fimbria (mean length 17.1±2.4cm, and mean weight 75.6±5.7g) were used to evaluate toxic effects on antioxidant systems, immune responses, and stress indicators by ammonia exposure (0, 0.25, 0.75, and 1.25mg/L) at different water temperature (12 and 17°C) in 1 and 2 months. In antioxidant responses, superoxide dismutase (SOD) and catalase (CAT) were significantly increased by ammonia exposure, whereas glutathione (GSH) was decreased. In immune responses, lysozyme and phagocytosis activity were significantly increased by ammonia exposure. In stress indicators, plasma glucose, heat shock protein 70 (HSP 70), and cortisol were significantly increased. At high water temperature (17°C), alterations by ammonia exposure were more distinctly. The results of this study indicated that ammonia exposure can induce toxic effects in the sablefish, and high water temperature can affect the ammonia exposure toxicity.


Subject(s)
Ammonia/toxicity , Perciformes , Water Pollutants, Chemical/toxicity , Animals , Catalase/metabolism , Fish Proteins/metabolism , Gills/drug effects , Gills/metabolism , Glutathione/metabolism , HSP70 Heat-Shock Proteins/metabolism , Hydrocortisone/blood , Kidney/drug effects , Kidney/metabolism , Liver/drug effects , Liver/metabolism , Micrococcus , Muramidase/blood , Muramidase/metabolism , Perciformes/blood , Perciformes/immunology , Perciformes/metabolism , Phagocytosis , Superoxide Dismutase/metabolism , Temperature , Water
4.
J Med Food ; 19(1): 98-105, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26305727

ABSTRACT

Angelica sinensis (AS) is one of the most popular medicinal foods used as a hematopoietic herb and also traditionally applied topically for skin disorders. However, the effectiveness of AS on atopic dermatitis (AD) has not been reported yet. This study was conducted to evaluate the antipruritic and anti-inflammatory effects of AS on regulating AD-related mediators in DNCB (2,4-dinitrochlorobenzene)-induced mice. AS was topically applied to the dorsal skin of DNCB-challenged mice for 11 days. Alteration of skin thickness was measured for assessment of histological improvement. In addition, the number of mast cells, the level of serum immunoglobulin E (IgE), the counting of scratching behavior, and the expression of substance P were evaluated. Also, the expressions of cytokines, nuclear factor κB (NF-κB), phospho-IκBα, and mitogen-activated protein kinases (MAPKs) were measured for evaluating the improvement of skin inflammation. The repeated treatment of AS significantly inhibited the skin thickness, the number of mast cells, and the level of serum IgE. Moreover, AS significantly suppressed the increased scratching behavior and the expression of substance P compared to the DNCB group. Topical application of AS also reduced the level of cytokines (IL-4, IL-6, TNF-α, and IFN-γ) as well as the expressions of NF-κB, phospho-IκBα, and phospho-MAPKs in the dorsal skin. The results of our study suggest that topical application of AS might have efficacy for modulating pruritus and inflammation in AD. Further studies are required to further characterize the mechanism of actions of AS.


Subject(s)
Angelica sinensis/chemistry , Dermatitis, Atopic/drug therapy , Dermatitis, Atopic/immunology , Plant Extracts/administration & dosage , Pruritus/drug therapy , Pruritus/immunology , Animals , Dermatitis, Atopic/genetics , Female , Humans , Immunoglobulin E/genetics , Immunoglobulin E/immunology , Interleukin-4/genetics , Interleukin-4/immunology , Interleukin-6/genetics , Interleukin-6/immunology , Mice , Mice, Inbred BALB C , NF-kappa B/genetics , NF-kappa B/immunology , Pruritus/genetics , Skin/drug effects , Skin/immunology , Tumor Necrosis Factor-alpha/genetics , Tumor Necrosis Factor-alpha/immunology
5.
Phytother Res ; 29(10): 1616-21, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26174209

ABSTRACT

Lonicera japonica Thunb. (Caprifoliaceae) is a traditional herbal medicine and has been used to treat diabetic symptoms. Notwithstanding its use, the scientific basis on anti-diabetic properties of L. japonica is not yet established. This study is designed to investigate anti-diabetic effects of L. japonica in type 2 diabetic rats. L. japonica was orally administered at the dose of 100 mg/kg in high-fat diet-fed and low-dose streptozotocin-induced rats. After the treatment of 4 weeks, L. japonica reduced high blood glucose level and homeostatic model assessment of insulin resistance in diabetic rats. In addition, body weight and food intake were restored by the L. japonica treatment. In the histopathologic examination, the amelioration of damaged ß-islet in pancreas was observed in L. japonica-treated diabetic rats. The administration of L. japonica elevated peroxisome proliferator-activated receptor gamma and insulin receptor subunit-1 protein expressions. The results demonstrated that L. japonica had anti-diabetic effects in type 2 diabetic rats via the peroxisome proliferator-activated receptor gamma regulatory action of L. japonica as a potential mechanism.


Subject(s)
Diabetes Mellitus, Type 2/drug therapy , Lonicera , PPAR gamma/metabolism , Phytotherapy , Plant Extracts/pharmacology , Animals , Body Weight , Diabetes Mellitus, Experimental/drug therapy , Diabetes Mellitus, Type 2/metabolism , Diet, High-Fat , Hyperglycemia/drug therapy , Insulin Resistance , Male , Plants, Medicinal , Rats , Streptozocin
6.
Food Funct ; 5(7): 1594-601, 2014 Jul 25.
Article in English | MEDLINE | ID: mdl-24881676

ABSTRACT

Estrogen deficiency in menopausal women is the main cause of osteoporosis. Phytoestrogen could be a suitable candidate for treatment of post-menopausal osteoporosis. Recent studies showed that S. chinensis contains several lignans, which may be phytoestrogen. In this study, we investigated the ameliorative effects of S. chinensis on post-menopausal osteoporosis. 30% ethanol extract of S. chinensis (SC) was administered orally for 6 weeks after 7 weeks of ovariectomized-induced osteoporosis. Bone mineral density was significantly increased following increased serum osteocalcin levels by SC treatment. Histological analysis showed that SC reduced the increased growth plate of the epiphyseal plate in femur. In addition, pores within bone marrow cells filling the lateral and medial epicondyle were decreased. Serum estradiol concentration was significantly increased in the SC-treated group. The expressions of estrogen receptor-α and -ß were increased in uterus and MCF-7 breast cancer cells by SC treatment. And two transcriptions of proto-oncogenes, c-fos and c-Jun, were suppressed by treatment of SC. From these data, we propose that S. chinensis attenuates post-menopausal osteoporosis with its phytoestrogenic effects. S. chinensis may have the potential to be used as an alternative for treatment of osteoporosis.


Subject(s)
Osteoporosis, Postmenopausal/drug therapy , Phytotherapy , Plant Extracts/administration & dosage , Receptors, Estrogen/metabolism , Schisandra/chemistry , Administration, Oral , Alanine Transaminase/blood , Animals , Aspartate Aminotransferases/blood , Blood Urea Nitrogen , Bone Density/drug effects , Cell Survival/drug effects , Creatinine/blood , Estradiol/blood , Female , Femur/drug effects , Femur/metabolism , Humans , MCF-7 Cells , Mice, Inbred ICR , Organ Size/drug effects , Osteocalcin/blood , Phytoestrogens/administration & dosage , Proto-Oncogene Proteins c-fos/genetics , Proto-Oncogene Proteins c-fos/metabolism , Proto-Oncogene Proteins c-jun/genetics , Proto-Oncogene Proteins c-jun/metabolism , Uterus/drug effects , Uterus/metabolism , ERRalpha Estrogen-Related Receptor
7.
Arch Virol ; 159(10): 2549-57, 2014 Oct.
Article in English | MEDLINE | ID: mdl-24810099

ABSTRACT

HBx acts as a multifunctional regulator that modulates various cellular responses, which can lead to development and progression of hepatocellular carcinoma (HCC). Here, we show that the HBx protein is also localized to peroxisomes, and this increases cellular reactive oxygen species (ROS) to levels that are higher than when HBx is localized to other organelles. The elevated ROS strongly activated nuclear factor (NF)-κB. In addition, the peroxisome-localized HBx increased the expressions of matrix metalloproteinases and decreased the expression of E-cadherin, which increased the invasive ability of HCC cells. Thus, a specific distribution of HBx to peroxisomes may contribute to HCC progression by increasing the invasive ability of HCC cells through elevation of the cellular ROS level.


Subject(s)
Carcinoma, Hepatocellular/pathology , Liver Neoplasms/pathology , Peroxisomes/metabolism , Reactive Oxygen Species/metabolism , Trans-Activators/metabolism , Cadherins/biosynthesis , Cell Line, Tumor , Cell Transformation, Neoplastic/pathology , Disease Progression , HEK293 Cells , Hep G2 Cells , Hepatitis B/virology , Hepatitis B virus/pathogenicity , Humans , Matrix Metalloproteinase 1/biosynthesis , Matrix Metalloproteinase 1/genetics , Matrix Metalloproteinase 7/biosynthesis , Matrix Metalloproteinase 7/genetics , Matrix Metalloproteinase 9/biosynthesis , Matrix Metalloproteinase 9/genetics , Membrane Potential, Mitochondrial , Mitochondria/pathology , NF-kappa B/biosynthesis , Neoplasm Invasiveness , RNA, Messenger/biosynthesis , Viral Regulatory and Accessory Proteins
8.
Int Immunopharmacol ; 19(2): 214-20, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24503166

ABSTRACT

Cortex Phellodendri amurensis (CPA), derived from the dried bark of Phellodendron amurense Rupr., is a traditional medicine widely used to treat various inflammation-related diseases. The aim of this study was to investigate the anti-inflammatory activity and molecular mechanism of CPA in vivo and in vitro. Mice were pretreated with CPA (200 mg/kg, p.o.) for three consecutive days; 2h after the last CPA treatment, mice were intraperitoneally injected with lipopolysaccharide (LPS) to induce endotoxemia (35 mg/kg). After treatment, we assessed survival rate, protein levels and cytokine expression. In addition, we confirmed the molecular mechanism of anti-inflammatory effects of CPA in LPS-stimulated macrophage RAW 264.7 cells. The results showed that CPA significantly increased mice survival rates and down-regulated LPS-induced interleukin (IL)-6, IL-1ß and macrophage chemo-attractant protein (MCP)-1 in serum. In addition, CPA inhibited inducible nitric oxide synthase (iNOS), activation of nuclear factor (NF)-κB by degradation and phosphorylation of IκBα, and attenuated phosphorylation of mitogen-activated protein kinases (MAPKs; ERK 1/2, p38 and JNK) from mice challenged with LPS. Moreover, in RAW 264.7 cells, CPA dose-dependently down-regulated LPS-stimulated NO, iNOS expression, as well as inflammatory cytokines and protein expression, consistent with the results in vivo. The anti-inflammatory properties of CPA in vitro and in vivo suggest its utility for attenuating inflammation-related diseases.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Endotoxemia/metabolism , Phellodendron , Plant Extracts/pharmacology , Animals , Anti-Inflammatory Agents/chemistry , Anti-Inflammatory Agents/therapeutic use , Berberine/analysis , Cell Line , Cyclooxygenase 2/metabolism , Cytokines/metabolism , Down-Regulation , Endotoxemia/drug therapy , Female , Lipopolysaccharides , Medicine, Chinese Traditional , Mice , Mice, Inbred ICR , Mitogen-Activated Protein Kinases/metabolism , NF-kappa B/metabolism , Nitric Oxide/metabolism , Nitric Oxide Synthase Type II/metabolism , Phellodendron/chemistry , Plant Bark/chemistry , Plant Extracts/chemistry , Plant Extracts/therapeutic use
9.
Appl Opt ; 49(9): 1666-70, 2010 Mar 20.
Article in English | MEDLINE | ID: mdl-20300165

ABSTRACT

We have generated continuous-wave single-frequency 1.5 W 378 nm radiation by frequency doubling a high-power Ti:sapphire laser in an external enhancement cavity. An LBO crystal that is Brewster-cut and antireflection coated on both ends is used for a long-term stable frequency doubling. By optimizing the input coupler's reflectivity, we could generate 1.5 W 378 nm radiation from a 5 W 756 nm Ti:sapphire laser. According to our knowledge, this is the highest CW frequency-doubled power of a Ti:sapphire laser.

10.
Opt Express ; 16(7): 4866-71, 2008 Mar 31.
Article in English | MEDLINE | ID: mdl-18542585

ABSTRACT

We have developed a 5-W 756-nm injection-locked Ti:sapphire laser and frequency-doubled it in an external enhancement cavity for the generation of watt-level 378-nm single-frequency radiation, which is essential for isotope-selective optical pumping of thallium atoms. With a lithium triborate (LBO) crystal in the enhancement cavity, 1.1 W at 378 nm was coupled out from the cavity. Such results are to our knowledge the highest powers of continuous-wave single-frequency radiation generated from a Ti:sapphire laser and its frequency doubling.


Subject(s)
Aluminum Oxide , Computer-Aided Design , Lasers , Models, Theoretical , Titanium , Computer Simulation , Equipment Design , Equipment Failure Analysis
11.
Appl Opt ; 46(28): 6854-8, 2007 Oct 01.
Article in English | MEDLINE | ID: mdl-17906710

ABSTRACT

We have analyzed the temporal characteristics of amplified spontaneous emission (ASE) in femtosecond terawatt Ti:sapphire lasers by using a simple method based on fast photodiodes. Instead of measuring ASE directly with fast photodiodes, we created a narrow gap in the spectrum of seed pulses and, after amplification, detected the pure ASE signal through the gap by using a fast photodiode covered with a bandpass filter with high transmission at the gap. Because the detected ASE signal was completely separated from amplified main pulses, preceding and even trailing ASEs could be characterized quantitatively in a single-shot measurement. We believe that our method is a good alternative or a complement to conventional methods for ASE measurements.

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