Publications by authors named "Mai Yamashita"

TriQuinoline (TQ), a quasi-planar cyclic quinoline trimer concatenated at the 2,8-positions in a head-to-tail arrangement, strongly captures a proton at the 12-membered inner cycle and exhibits unusual physicochemical properties, including unexpected water solubility and the ability to engage in complexation with other π-conjugated molecules. In this study, we designed and synthesized its expanded analog, coined Enlarged-TriQuinoline (Enl-TQ), in which three alkyne units are embedded between three quinoline units to acquire an expanded planar 18-membered ring system. DFT calculations and X-ray crystallographic analysis revealed its planar architecture with three inwardly facing pyridinic nitrogen atoms.

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  • This study evaluated the effectiveness and safety of four JAK inhibitors (tofacitinib, baricitinib, peficitinib, and upadacitinib) in treating rheumatoid arthritis in a real-world setting, focusing on reducing bias and adjusting for patient characteristics.
  • A total of 622 patients were analyzed, with no significant differences found in retention rates, disease activity scores, or remission rates among the various treatment groups after 6 months.
  • Key predictive factors for treatment efficacy included baseline disease activity and previous treatment history, but overall, the four drugs showed similar effectiveness and safety in managing rheumatoid arthritis.
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  • The study aimed to assess changes in disease activity among elderly RA patients over 75 years old in Japan from 2014 to 2021.
  • Data showed an increase in the percentage of elderly patients achieving remission and low disease activity (LDA), with rates rising from 62.2% to 78.2% during that time.
  • Factors that positively influenced remission and LDA included the use of methotrexate, while glucocorticoid use and previous b/tsDMARDs treatments negatively impacted these outcomes.
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  • Pancreatic ductal adenocarcinoma (PDAC) is a highly lethal cancer with issues such as side effects from treatments and drug resistance in cancer stem cells (CSCs).
  • The study suggests that cyclic guanosine monophosphate (cGMP) can reduce mitochondrial function in PDACs and impair CSC characteristics through energy-related pathways.
  • Results indicated that cGMP increases the PPARα/PDK4 pathway, leading to better outcomes for patients with high PDK4 gene expression, presenting potential new targets for treating pancreatic CSCs.
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  • Drug-induced lupus (DIL) symptoms often mirror systemic lupus erythematosus (SLE) and typically resolve after stopping the causative medication.
  • A 41-year-old woman with ulcerative colitis exhibited polyarthritis, myositis, and tested positive for anti-dsDNA antibodies, leading to a DIL diagnosis post cessation of mesalazine.
  • Six months later, she developed lupus myocarditis but showed significant improvement after treatment with glucocorticoids, cyclophosphamide, IV immunoglobulin, and an intra-aortic balloon pump, highlighting the need for careful monitoring of DIL patients with antibody predispositions.
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A 57-year-old woman was referred for progressive dyspnea. CT showed a tracheal mass, suspicious of tracheal neoplasm. The lesion was partially resected, and nonspecific granulation tissue was observed on histology.

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We compared the prophylactic effect of trimethoprim-sulfamethoxazole (TMP-SMX) with atovaquone for pneumocystis pneumonia (PCP) in patients with connective tissue diseases (CTDs) receiving high-dose glucocorticoids. Patients with CTDs aged ≥ 18 years who were treated with a prolonged course (≥ 4 weeks) of glucocorticoids (≥ 20 mg/day prednisone) in a Japanese tertiary center between 2013 and 2017 were included. The patients were categorized into two groups: TMP-SMX and atovaquone group.

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We examined whether oral administration of a hop-derived prenylflavonoid isoxanthohumol (IX) would show anti-obesity activity and the underlying mechanism of the potential activity using a high-fat diet (HFD)-induced obese mouse model. Oral administration of 180 mg/kg IX for 8 weeks suppressed HFD-induced accumulation of visceral fat and body weight gain in mice. Simultaneously, IX changed the composition of the microbiome, as determined by a significant increase in the relative abundances of , , and .

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The aim of this study was to verify the effect of treatment with isoxanthohumol (IX) on the metabolomics profile of mouse feces to explore the host-intestinal bacterial interactions at the molecular level. The fecal contents of several amino acids in the high-fat diet (HFD) + 0.1% IX group (treated with IX mixed in diets for 12 weeks) were significantly lower than in the HFD group.

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TLR signaling is critical to innate immune system regulation; however, aberrant TLR signaling is involved in several diseases, including insulin resistance, Alzheimer's disease, and tumor metastasis. Moreover, a recent study found that TLR-4 signaling pathway inhibition might be a target for the suppression of chronic inflammatory disorders. In this article, we show that the green tea polyphenol epigallocatechin-3--gallate (EGCG) increases the expression of Toll interacting protein, a strong inhibitor of TLR4 signaling, by suppressing the expression of E74-like ETS transcription factor 1 (Elf-1).

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Toll-like receptor 4 (TLR4) plays an essential role in innate immunity through inflammatory cytokine induction. Recent studies demonstrated that the abnormal activation of TLR4 has a pivotal role in obesity-induced inflammation, which is associated with several diseases, including hyperinsulinemia, hypertriglyceridemia, and cardiovascular disease. Here we demonstrate that (-)-epigallocatechin-3--gallate, a natural agonist of the 67-kDa laminin receptor (67LR), suppressed TLR4 expression through E3 ubiquitin-protein ring finger protein 216 (RNF216) up-regulation.

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  • Western diets lead to obesity, which is linked to higher cholesterol and increased risk of cardiovascular disease.
  • In an experiment with male mice, those fed a high-fat and high-sucrose diet with both green tea extract and eriodictyol lost more weight and had significantly lower cholesterol and LDL levels compared to those on the high-fat diet alone.
  • The combination of green tea and eriodictyol improved liver function by lowering the expression of cholesterol-related enzymes and increasing LDL receptor levels, suggesting a potential dietary strategy to combat high cholesterol.
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Suppression subtractive hybridization was used to identify genes showing differential expression profile associated with growth rate in skeletal muscle tissue of Landrace weanling pig. Two subtracted cDNA populations were generated from musculus longissimus muscle tissues of selected pigs with extreme expected breeding values at the age of 100 kg. Three upregulated genes (EEF1A2, TSG101 and TTN) and six downregulated genes (ATP5B, ATP5C1, COQ3, HADHA, MYH1 and MYH7) in pig with genetic propensity for higher growth rate were identified by sequence analysis of 12 differentially expressed clones selected by differential screening following the generation of the subtracted cDNA population.

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Relapsing polychondritis (RP) is a rare autoimmune disease affecting the multiple organ system. Here, we describe a case of RP initially presenting with high fever. The patient was referred to our hospital for further examination of fever of unknown origin (FUO).

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Chronic widespread pain is a serious medical problem, yet the mechanisms of nociception and pain are poorly understood. Using a reserpine-induced pain model originally reported as a putative animal model for fibromyalgia, this study was undertaken to examine the following: (1) expression of several ion channels responsible for pain, mechanotransduction, and generation/propagation of action potentials in the dorsal root ganglion (DRG), (2) activities of peripheral nociceptive afferents, and (3) alterations in spinal microglial cells. A significant increase in mRNA expression of the acid-sensing ion channel (ASIC)-3 was detected in the DRG, and the behavioral mechanical hyperalgesia was significantly reversed by subcutaneous injection of APETx2, a selective blocker of ASIC3.

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