Publications by authors named "Yan Bo Wang"

In this manuscript, we comment on the article by Liu published in the recent issue of the journal. Hyperuricemia (HUA) has become the second most common metabolic disease after type 2 diabetes mellitus and is the most important risk factor for gout. This discussion focuses on the targets and clinical application value of traditional Chinese medicine (TCM) extracts in the treatment of HUA and gout, emphasizing the role of gut microbiota.

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  • Current guidelines suggest that patients with atrial fibrillation (AF) should maintain a resting heart rate below 100-110 bpm, but there is limited research on treatment options specifically for those also dealing with coronary heart disease (AF&CHD).
  • A study analyzed data from nearly 4,000 participants in the AFFIRM trial, finding that patients with AF&CHD had a higher prevalence of various health issues and a significantly increased risk of all-cause mortality compared to those with AF alone (RR = 1.79).
  • The study suggests that an optimal resting heart rate for AF&CHD patients is around 70 bpm, with lower mortality rates associated with resting heart rates below this threshold.
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Clothianidin (CLO) is a high-frequently detected neonicotinoid pesticide in fruits and vegetables, whose exposure security deserves attention. This study evaluated the apoptotic toxicity of CLO on Caco-2 cells at doses of 100 nM, 10 μM, and 1 mM. After exposure, CLO induced to a remarkable change of signaling proteins that participated in the process of cell apoptosis, including caspase 3, cleaved-caspase 3, and caspase 9.

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  • This study explores the fermentation characteristics of Bacillus velezensis D6, focusing on the co-production of two enzymes, α-amylase and protease, and their potential applications in fermentation processes.
  • The research found optimal production conditions, achieving high enzyme activity levels, and demonstrated that both enzymes are thermally stable and effective over a range of pH levels.
  • The α-amylase showed significant hydrolysis efficiency on various starchy substrates, while the protease effectively hydrolyzed animal-based proteins, indicating their practical applications in food processing.
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An effective and straightforward Ag(I)-mediated annulation of 2-(2-enynyl)quinolines and -(2-alkynylbenzylidene)hydrazides was developed, forging various synthetically challenging 17-isoquinolino[2'',1'':1',6']pyridazino[4',5':3,4]pyrrolo[1,2-]quinolines, including different nitrogen-containing fused rings, in moderate to excellent yields. This one-pot cycloaddition strategy features exclusive regioselectivity, high atom economy, and broad substrate scope under mild conditions. The practicality and reliability of this cycloaddition reaction was demonstrated by a successful scale-up synthesis.

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Exposure to pesticides induces oxidative stress and deleterious effects on various tissues in non-target organisms. Numerous models investigating pesticide exposure have demonstrated metabolic disturbances such as imbalances in amino acid levels within the organism. One potentially effective strategy to mitigate pesticide toxicity involves dietary intervention by supplementing exogenous amino acids and their derivates to augment the body's antioxidant capacity and mitigate pesticide-induced oxidative harm, whose mechanism including bolstering glutathione synthesis, regulating arginine-NO metabolism, mitochondria-related oxidative stress, and the open of ion channels, as well as enhancing intestinal microecology.

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  • This study analyzed 10 types of functional vinegars, identifying various bioactive compounds including flavonoids, phenolics, and saponins, which contribute to their health benefits.
  • Significant variations in antioxidant activities and concentrations of polysaccharides and organic acids were observed, with some compounds like tartaric and chlorogenic acids showing a positive correlation with antioxidant capacity.
  • New physiologically active ingredients were discovered in the functional vinegars, and specific volatile compounds were linked to their antioxidant effectiveness, highlighting the diversity of beneficial substances in these traditional products.
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An effective Ag(I)-mediated annulation of 2-(2-enynyl)pyridines and propargyl amines was developed, unexpectedly affording a broad range of functionalized 1-(2-pyrrol-3-yl)indolizines in moderate to excellent yields. The developed method is characterized by operational simplicity, ready availability of starting materials, high regioselectivity, and broad substrate scope under mild reaction conditions. The Ag(I)-promoted cyclization of 2-(2-enynyl)pyridines and propargyl amines possibly results in the formation of the spiroindolizine, the ring-opening rearrangement of which may give the 1-(2-pyrrol-3-yl)indolizine.

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A simple and efficient base-mediated decarboxylative annulation of ynones with methyl 2-(2-bromophenyl)acetates has been developed. A broad range of benzoxepines were prepared with a broad substrate scope and high regioselectivity in moderate to excellent yields under transition-metal-free conditions. This method proceeds through a tandem [2 + 4] annulation, ring-opening decarboxylative reaction, and the intramolecular nucleophilic aromatic substitution reaction.

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The methodology for the synthesis of fluorene-based atropisomers was developed via the strategy of aromatic ring formation. By this strategy, an efficient benzannulation of indene-based diene with benzoylacetonitrile divergently promoted by DABCO and a chiral organocatalyst was established, and various atropisomeric fluorene-based skeletons were generated in good yields, which not only provide a new strategy for the construction of atropisomeric biaryls but also offer a new member to the atropisomeric family.

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A facile and effective tandem reaction of ynones and methyl salicylates was developed to obtain a broad range of 3-acyl chromones in moderate-to-excellent yields. This protocol underwent a Michael addition and cyclization process, which exhibited easily accessible substrates, broad substrate scope, and high regioselectivity under mild and transition-metal-free conditions. Moreover, gram-scale reaction and further chemical transformation of the products were also further studied.

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A facile and efficient base-mediated divergent annulation of methyl 2-(cyanomethyl)benzoates and conjugated ynones has been described. A broad range of 1-naphthols and xanthones were formed in moderate to excellent yields. The notable features of this protocol include readily available precursors, broad substrate scope, complete regioselectivity, and substrate-controlled divergent synthesis.

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Objective: To assess the effect of dl-3-n-butylphthalide (NBP) on angiogenesis and its underlying mechanism in a rat model of chronic myocardial ischemia (CMI).

Methods: Forty Sprague-Dawley rats were randomly divided into four groups: model, low-dose NBP (L-NBP), middle-dose NBP (M-NBP), or high-dose NBP (H-NBP) (n=10/group). All groups received intraperitoneal injections of isoprinosine hydrochloride daily for 14 days.

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  • The study aimed to evaluate how the medication sacubitril/valsartan affects right ventricular (RV) function in patients with pulmonary hypertension (PH) caused by heart failure with reduced ejection fraction (HFrEF).
  • A total of patients with HFrEF-induced PH were given either sacubitril/valsartan or enalapril for 6 months, with assessments through echocardiography conducted at the start and after treatment.
  • Results showed that sacubitril/valsartan significantly improved key heart function metrics compared to enalapril, indicating it has more beneficial effects on RV function and reduces pulmonary pressure in these patients.
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Objective: To compare the clinical efficacy between 's scalp acupuncture combined with virtual reality (VR) rehabilitation training and VR rehabilitation training alone for motor dysfunction in patients with Parkinson's disease (PD).

Methods: A total of 52 patients with PD were randomly divided into an observation group and a control group, 26 cases in each group. The patients in both groups were treated with routine basic treatment, and the patients in the control group were treated with VR rehabilitation training.

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Ear architecture is determined by two stable heritable traits, kernel row number (KRN) and kernel number per row (KNPR), but its relationship with drought resistance is still vague. To this end, we obtained 16 and 11 hybrids with slender (less KRN but more KNPR) and stubby (more KRN but less KNPR) ears by intentionally crossbreeding, respectively. These hybrids were exposed to a seven-day water deficit (WD) since silk emergence coupled with synchronous (SP) and continuous pollination (CP) to alter the pollination time gaps on ears.

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Tropomyosin (TM) is an important crustacean () allergen. This study aimed to assess Maillard-reacted TM (TM-G) induction of allergenic responses with cell and mouse models. We analyzed the difference of sensitization and the ability to induce immune tolerance between TM and TM-G by in vitro and in vivo models, then we compared the relationship between glycation sites of TM-G and epitopes of TM.

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In line with the Healthy China strategy, new requirements for medical education have been raised. Medical education against the background of a new model of medicine demands an effective response to its inherent complex elements concerning the rule of law. During the course of the implementation of the new medicine strategy, in face of the widening scope of medical risks, the growing awareness of patient rights, and the conventional logic of medical education, elements concerning the rule of law should be incorporated in medical education in the early stage so as to help medical practitioners develop the appropriate legal literacy and rely on ideas of rules, equality and ethical bottomlines to analyze and solve problems.

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A simple and effective tandem reaction of diynones and allylic alcohols was developed to afford functionalized 3-allyl-4-pyrones in moderate to excellent yields. This protocol underwent a Michael addition─Claisen rearrangement─O-cyclization process, which exhibited broad substrate tolerance, high regioselectivity, and atom economy under a metal-free condition. Moreover, functional transformation of the products was also further studied.

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To explore effect of the structural properties of porphyra haitanensis polysaccharide on its biological activity, degraded porphyra polysaccharides were separated and purified by Cellulose DEAE-52 and Sephadex G-100 chromatography, obtaining three purified components (P1, P2 and P3). All the three components were sulfate polysaccharides containing the repeating units of → 3) β-D-galactose (1 → 4) 3,6-anhydro-α-L-galactose (1 →, and → 3) β-D-galactose (1 → 4) α-L-galactose-6-S (1 →, and → 3) 6-O-methyl-β-D-galactose (1 → 4) 3,6-anhydro-α-L-galactose (1 →. The molecular weight of the three fractions was measured to be 300.

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  • A new cascade reaction was developed using 1-indanylidenemalononitrile and 3-benzylidenebenzofuran-2(3)-one, which can be promoted by DABCO or a chiral organocatalyst under mild conditions.
  • The reaction produced a variety of spiro-dihydrofluorene-benzofuranones, and adjusting the reaction conditions allowed for the selective formation of either spiro or axially chiral products.
  • The study also included quantum chemical calculations to better understand the mechanism behind the transformation.
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The degraded polysaccharides from Porphyra yezoensis (DPPY) prepared using the H O -Vc method under optimized conditions were isolated and purified by DEAE Cellulose-52, and Sephadex G-100, providing four pure components, namely, DPPY-0, DPPY-0.1, DPPY-0.3, and DPPY-0.

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A simple and effective annulation of ynediones and (iso)quinoline -oxides was developed to afford various functionalized pyrrolo[2,1-]isoquinolines and pyrrolo[1,2-]quinolines in moderate to excellent yields. This protocol underwent a tandem [3 + 2] cycloaddition/ring-opening/-nucleophilic addition, which exhibited high regioselectivity, broad substrate tolerance, and atom economy under catalyst-, additive-free, and air conditions. Moreover, indolizine was also successfully prepared using pyridine -oxide.

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1-Indazolo[1,2-]phthalazine-5,10-dione IPDD with an approximate turbine-like spatial structure, primary assembled double-stranded helices at the first level, was predicted by quantum chemical calculations and confirmed by atomic force microscopy. The higher-dimensional hierarchical architectures including fibrils, helical fibers, spherical shells, and porous prismatic structures were observed in sequence by the scanning electron microscopy technique. The final porous prismatic structures sensitive to NH vapors have the potential to be applied in gas sensing and absorbing materials.

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