Publications by authors named "Huang You"

Intestinal injury of weaned piglets often leads to reduced immunity, diarrhea and growth retardation, resulting in significant economic losses to agriculture. Betulinic acid (BA) is a natural plant-derived active ingredient with multiple pharmacological activities including immune modulation and anti-inflammatory. This study was aimed to investigate the potential mechanism that BA as a feed additive mitigated lipopolysaccharide (LPS)-induced intestinal injury in piglets.

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Plant extracts, especially herbal extracts, are in line with the cosmetics development trend of natural and safe in today's world. Dried ginger essential oil (DGEO) is a fragrant oily liquid extracted from the dried roots of Zingiber officinale Rosc. This research investigated DGEO could effectively inhibit Staphylococcus aureus and Propionibacterium acnes.

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As a conventional immunosuppressive drug, cyclophosphamide (CYP) exhibits strong hepatotoxicity in clinical applications. Betulinic acid (BA) is a natural triterpenoid that protects against liver damage. However, the underlying mechanism has not yet been elucidated.

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Objectives: Cardiovascular disease (CVD) is the leading cause of death in China. This study compared ethnic disparities and lifestyle determinants in the prevalence of CVD (hypertension, coronary heart disease [CHD], and stroke) among older adults of the Han majority and Ha Ni ethnic minority in rural southwest China, to provide evidence for preventing and controlling CVD among older-adult minority communities.

Methods: A multi-stage stratified random sampling method was used to select 1,413 Han majority participants and 1,402 Ha Ni ethnic minority participants aged ≥ 60 years in rural Southwest China.

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Article Synopsis
  • Patchouli essential oil (PEO) shows promise for managing ulcerative colitis (UC) but is limited by poor absorption and stability.
  • A new nanoemulsion of PEO (PEONE) was created to improve its effectiveness for rectal delivery using a dual-sensitive hydrogel that helps target the inflammation site.
  • The PEONE@RTH formulation has been shown to reduce inflammation and oxidative stress in UC while also being safe and biocompatible, offering a potential new treatment strategy for UC and related intestinal disorders.
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Backgrounds: Ulcerative colitis (UC) is a form of chronic inflammatory bowel disease, and UC diagnosis rates continue to rise throughout the globe. The research and development of new drugs for the treatment of UC are urgent, and natural compounds are an important source. However, there is a lack of systematic summarization of natural compounds and their mechanisms for the treatment of UC.

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Article Synopsis
  • Pogostemonis Herba, known for its use in traditional Chinese medicine, has potential to treat ulcerative colitis (UC) primarily through its main component, patchouli essential oil (PEO), although its pharmacological mechanisms are not fully understood.
  • The study combined transcriptomic and network pharmacology methods, revealing that rectal administration of PEO in UC model mice significantly reduced UC symptoms by suppressing colonic inflammation and oxidative stress.
  • PEO appears to work by modulating gut microbiota, inhibiting key inflammatory targets, and blocking the PI3K-AKT pathway, with specific bioactive components like pogostone identified for further potential therapeutic applications against UC.
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Article Synopsis
  • A new method has been developed for catalyst-free reactions that combine Morita-Baylis-Hillman carbonates with sulfur ylides, leading to the creation of 1,2-dihydroquinolines.
  • This process showcases a wide range of applicable compounds, high selectivity for different chemical groups, and overall efficiency in synthesis.
  • Mechanistic studies indicate that the reaction involves a unique 1,1-dipole cross-olefination and that the amino group plays a crucial role in facilitating these transformations.
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Organocatalytic annulations between allenes and bisnucleophiles represent one of the most convenient routes to various carbocycles and heterocycles. However, most examples are limited to the formation of five- and six-membered rings, probably owing to relatively easy handling of short-chained biselectrophiles. Here we report long-chained α-allyl allenoate-derived 1,6-biselectrophiles for the first time, enabling a phosphine catalyzed [6 + 1] annulation with readily available 1,1-bisnucleophilic reagents.

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Viola yedoensis Makino (Vy) is a well-known traditional Chinese medicine widely used to treat inflammatory diseases. However, the regulatory effects of dietary Vy supplementation on lipopolysaccharide (LPS)-induced intestinal damage in broilers and the underlying molecular mechanisms remain unclear. In this study, broilers were intraperitoneally injected with 1 mg/kg LPS on days 17, 19 and 21 to induce intestinal damage.

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The CLE (CLAVATA3/Embryo Surrounding Region-related) family, a group of peptides with hormone-like features, plays a pivotal role in plant growth, development, and adaptation to stress. Through homology-based blast analysis of 32 CLE peptide sequences, we have identified 5, 14, and 10 CLE family members in , and , respectively. Chemical synthesis and functional assays of the peptides led to the discovery that NtCLE3 substantially enhances the drought resistance of these three Solanaceae crops.

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Background: Atractylodes macrocephala Koidz. (Baizhu in Chinese, BZ) is a typical traditional edible-medicinal herb used for thousands of years. Known as "the spleen-reinforcing medicine", it is often used clinically to treat reduced digestive function, abdominal distension, and diarrhoea, which are all caused by spleen deficiency.

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A novel phosphine-catalyzed domino annulation reaction of γ-vinyl allenoates and -aminotrifluoacetophenones for the construction of terahydrofuro[3,2-]quinoline derivatives has been developed. In this domino reaction, two kinds of terahydrofuro[3,2-]quinoline compounds containing CF groups were obtained with good yields under mild conditions, three new C-N, C-C, and C-O bonds can be built in one step, and the reaction selectivity is achieved by adjusting the reaction conditions. Furthermore, preliminary studies on an asymmetric variant of this reaction proceeded with moderate enantioselectivity.

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T-2 toxin, a type-A trichothecene mycotoxin, exists ubiquitously in mildewed foods and feeds. Betulinic acid (BA), a pentacyclic triterpenoid derived from plants, has the effect of relieving inflammation and oxidative stress. The purpose of this study was to investigate whether BA mitigates lung impairment caused by T-2 toxin and elucidate the underlying mechanism.

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The first (5+1) annulation of allenoates and pyrazolones catalyzed by CHOK has been reported. A series of spiro-pyrazolone derivatives were obtained as single diastereomers in high yields (≤95%) under mild conditions. The synthetic utility was demonstrated by a scale-up reaction and various transformations of the products.

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An unprecedented phosphine-catalyzed formal Buchner [6+1] annulation of a newly designed allenoate has been developed, providing a series of cycloheptatriene derivatives in moderate to good yields (up to 99%). This reaction demonstrates that the introduction of an electrophilic allylic group to allenoates effectively extends the reaction scope of phosphine-catalyzed annulation, providing a concise route to cycloheptatrienes. Mechanistic study indicated that this reaction involves a [4+2] Diels-Alder reaction and ring expansion of the bicyclo[4.

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Aryl amines are of constant interest in organic synthesis owing to their ubiquity in natural products, pharmaceuticals, and organic materials. However, C-H amination or pre-functionalization frequently results in uncontrollable site selectivity, over activation and the generation of inseparable mixtures of regio-isomers. Here we present a novel metal free Dötz-type aminobenzannulation reaction that circumvents the selectivity issues inherent in aromatic chemistry, as well as the use of stoichiometric unstable organolithium reagents and toxic chromium complexes.

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Strong fluorescence and high catalytic activities cannot be achieved simultaneously due to conflicts in free electron utilization, resulting in a lack of bioactivity of most near-infrared-II (NIR-II) fluorophores. To circumvent this challenge, we developed atomically precise Au clusters with strong NIR-II fluorescence ranging from 950 to 1300 nm exhibiting potent enzyme-mimetic activities through atomic engineering to create active Cu single-atom sites. The developed AuCu clusters show 18-fold higher antioxidant, 90-fold higher catalase-like, and 3-fold higher superoxide dismutase-like activities than Au clusters, with negligible fluorescence loss.

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Article Synopsis
  • A new chemical reaction has been developed that uses a Lewis base to create a specific type of compound through a formal [4 + 2] annulation process.
  • The reaction combines acylamino-aryl MBH carbonates with electron-deficient olefins, resulting in the formation of tetrahydroquinolines.
  • These tetrahydroquinolines have three stereogenic centers, including a quaternary stereocenter, and are produced in high yields with good enantioselectivity.
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Near-infrared-II (NIR-II) imaging has shown great potential for monitoring the pathological progression and deep tissue imaging but is limited to present unmet NIR-II agent. Present fluorophores show a promising prospect for NIR-II imaging, but brightness and photostability are still highly challenging during real-time monitoring. In this work, atom-engineered NIR-II Au Cd  clusters with ultrahigh brightness, stability, and photostability are developed via single atomic Cd doping.

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Steel slag has been commonly used in road engineering as cementitious material; however, its application in base course is not widely reported. Four contents of steel slag (0%, 30%, 50%, 75% by volume) were blended into different cement (3%, 4%, 5%, 6% by weight)-treated aggregates. Mechanical properties, volume stability, economic benefits and environmental influences of steel slag mixtures were investigated for the feasibility of applying steel slag in semi-rigid base course.

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Aldolase A (ALDOA), an important metabolic enzyme in the glycolytic pathway, plays an important role in regulating tumour metabolism. In this study, we investigated the expression pattern of ALDOA in hepatocellular carcinoma (HCC) and its biological role in tumour progression. Bioinformatics analysis, western blot (WB) and RT-qPCR were performed to detect the relative expression of ALDOA in HCC tissues and cell lines.

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Betulinic acid (BA), an occurring pentacyclic triterpenoid, has various biological activities, such as anti-inflammation and antioxidation. Previous studies found that BA attenuated cyclophosphamide (CYP)-induced intestinal mucosal damage by inhibiting intestinal mucosal barrier dysfunctions and cell apoptosis. However, the effects and regulation mechanisms of BA on CYP-induced renal damage has not been reported in literature.

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Endoplasmic reticulum stress (ERS) plays a vital role in the pathogenesis of the alcoholic liver disease (ALD). Betulinic acid (BA) has been reported to be effective in the attenuation of ALD; however, its role in ERS and associated stress-signaling pathways remains elusive. Here, we found that the BA pretreatment significantly reduced the alcohol-induced liver injury by decreasing the activities of serum alanine aminotransferase and aspartate aminotransferase, alleviating fat deposition and rupturing the ER in hepatocytes.

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