Publications by authors named "Huawu Gao"

Neurodegenerative disorders are typically caused by harmful protein accumulation and nerve cell damage. A post-translational modification called O-linked N-acetylglucosamine ylation acts as a critical regulator in these disorders by controlling protein behavior, cell signaling, and energy balance. This modification is dynamically balanced through the cooperative actions of O-linked N-acetylglucosamine transferase and O-GlcNAcase.

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  • The study investigates how Huangdi Anxiao Capsules (HDAX) can protect rat adrenal pheochromocytoma (PC12) cells from cognitive dysfunction caused by high glucose levels, focusing on the NLRP3-mediated pyroptosis mechanism.
  • PC12 cells were divided into several groups to assess the effects of HDAX and the NLRP3 inhibitor mcc950 on cell viability and pyroptosis indicators using various assays.
  • Results showed that the model group (high glucose) had reduced cell survival and increased inflammatory markers, while both HDAX and mcc950 treatments improved cell health and reduced markers of pyroptosis compared to the model group.
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  • Genistein (GS), an isoflavone in soybeans, shows promise as a neuroprotective agent in Alzheimer's disease, but its mechanism isn't fully understood.
  • Research utilizing molecular docking and in vivo/in vitro studies found that GS improves learning and memory in AD rats, while reducing damage in hippocampal neurons and decreasing levels of specific proteins associated with cell death.
  • Overall, the findings suggest that GS could be a potential therapeutic target for Alzheimer's by inhibiting pathways linked to neuron apoptosis.
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Objectives: Chrysophanol (CHR), also well-known as Rhei radix et rhizome, is a crucial component in traditional Chinese medicine. It has been widely studied as a potential treatment for many diseases due to its anti-inflammatory effects. However, there are very few studies to establish the potential therapeutic effect of CHR in cell and animal models of Alzheimer's disease (AD).

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Background: Huang-Pu-Tong-Qiao formula (HPTQ), a traditional Chinese medicine (TCM) formula used to improve cognitive impairment. However, the underlying neuroprotective mechanism of HPTQ treated for diabetic cognitive dysfunction (DCD) remains unclear. The purpose of this study was to investigate the neuroprotective mechanism of HPTQ in DCD mice based on molecular docking.

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Alzheimer's disease (AD) is a complex neurodegenerative disease. It is a chronic, lethal disease in which brain function is severely impaired and neuronal damage is irreversible. Huang-Pu-Tong-Qiao (HPTQ), a formula from traditional Chinese medicine, has been used in the clinical treatment of AD for many years, with remarkable effects.

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Background: Growing evidences have been revealing that long noncoding RNAs are vital factors in oncogenesis and tumor development. Among them, cancer susceptibility candidate 11 (CASC11) has displayed an impressively essential role in various kinds of cancers including hepatocellular carcinoma (HCC). Nevertheless, its role and potential mechanism in HCC still remain to be fully investigated.

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  • Alzheimer's disease (AD) has a complex relationship with the renin-angiotensin system (RAS), which commonly influences cerebrovascular health and is linked to AD’s progression.
  • Existing research has highlighted the involvement of RAS components, like Ang II and Ang III, in cognitive decline and nerve injury in AD, connecting them to neuroinflammation, oxidative stress, and amyloid-β protein hypotheses.
  • This review emphasizes the need to carefully consider RAS in AD's pathogenesis and explores potential RAS-targeting drugs that could serve as new therapeutic options.
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This study is aimed to investigate the protective effect against type 2 diabetes mellitus (T2DM) and Alzheimer's disease (AD) of Berberine (BBR), and the underlying mechanism of action is explored. We established a rat model of combined AD and T2DM and used it to investigate the effect of BBR (150 mg/kg) on the course of these pathologies. The Morris water maze, biochemical analysis, hematoxylin-eosin staining, immunohistochemical study, immunofluorescent staining, TUNEL assay, RT-qPCR and western blot were used to reveal the effect of BBR on blood glucose, lipid changes, hippocampal injuries and cognitive impairment.

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Objective: To investigate the neuroprotective effect of chrysophanol (CHR) on PC12 treated with Aβ, and the involved mechanism.

Methods: After the establishment of an AD cell model induced by Aβ, the cell survival rate was detected by MTT, cell apoptosis was assayed by Hoechst 33342 staining, mRNA expressions of calmodulin (CaM), calcium/calmodulin-dependent protein kinase kinase (CaMKK), calcium/calmodulin-dependent protein kinase IV (CaMKIV) and tau (MAPT; commonly known as tau) were determined by qRT-PCR, and protein levels of CaM, CaMKK, CaMKIV, phospho-CaMKIV (p-CaMKIV), tau and phospho-tau (p-tau) were detected by Western blot analysis.

Results: When pretreated with CHR before exposure to Aβ, PC12 cells showed that increased cell viability and reduced apoptosis.

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Objectives: Alzheimer's disease (AD) is a hidden neurological degenerative disease, which main clinical manifestations are cognitive dysfunction, memory impairment and mental disorders. Neuroinflammation is considered as a basic response of the central nervous system. NLRP3 (Nucleotide-binding domain leucine-rich repeat (NLR) and pyrin domain containing receptor 3) inflammasome is closely related to the occurrence of neuroinflammation.

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Huangpu Tongqiao Capsules(HPTQC), with the functions of invigorating Qi and kidney, eliminating phlegm and removing blood stasis, have the effect of treating Alzheimer's disease(AD), but its mechanism needs further exploration. To explore the relationship between the therapeutic mechanism of HPTQC on Alzheimer's disease and EGFR-PLCγ signal pathway, 40 healthy male SD rats were selected and divided into 4 groups randomly: sham operation group(sham), model group(model), HPTQC group(HPTQC), and nimodipine group(NMP). AD rat model was established by intraperitoneal injection of D-galactose combined with an intracerebral injection of amyloid-β peptide(25-35).

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This study was aimed to investigate the effect of Chrysophanol (CHR) on Alzheimer's disease. We also attempted to understand the potential mechanisms. An Alzheimer's disease rat model was established using an intraperitoneal injection of d-galactose combined with an intracerebral injection of amyloid-β peptide (25-35), and the effect of CHR on the learning and memory ability, the hippocampal neurons change, the ultrastructure of the hippocampal CA1 region, the protein levels of CaM, CaMKK, CaMKIV, p-CaMKIV and p-tau in the hippocampus of rats were studied.

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This paper was aimed to investigate the relationship between autophagy and NLRP3 inflammasome activation by studying the effect oftotal flavonoids in Scutellaria barbata (TF-SB) on autophagy in tumor cells and NLRP3 inflammasome, and to provide experimental evidence for further study of the anti-tumor mechanism of TF-SB. Mielanoma models were established by inoculating B16-F1 cell line to mice, and then were randomly divided into 5 groups (n=10 in each group): model control, positive control control(Rap, 1.5 mg•kg⁻¹), and TF-SB low, middle and high groups (50, 100 and 200 mg•kg⁻¹).

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To investigate the effect of the total flavonoids in Scutellaria barbata(TF-SB) against autophagy in tumor cells in vivo, and further determine whether the mechanism is correlated with the PI3K/AKT/mTOR pathway, which lead to autophagy-induced tumor cell death. Melanoma-bearing mice were prepared and divided into control group, rapamycin group (Rap 1.5 mg•kg⁻¹), and high, middle and low-dose TF-SB (200, 100, 50 mg•kg⁻¹) groups.

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Objective: To investigate the effects of sapindus saponins on myocardial inflammation mediated by Ang II/ p38MAPK signal pathway and cardiac hypertrophy in spontaneously hypertensive rats. And also to explore the correlation of cardiac hypertrophy and inflammation.

Method: Thirty-two 16-week-old spontaneously hypertensive rats (SHR) were randomly divided into four groups, one with placebo as model group, one with captopril tablets (27 mg x kg(-1)) as positive control, one with low-dose sapindus saponins (27 mg x kg(-1)), one with high-dose (108 mg x kg(-1)).

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  • The study aimed to explore how sapindus saponins affect endothelial function in spontaneously hypertensive rats by analyzing their response to various vasoconstrictors and dilators, as well as measuring active substance levels.
  • Forty hypertensive rats were divided into different treatment groups, receiving either a placebo, a positive control, or varying doses of sapindus saponins over eight weeks, compared to a healthy control group.
  • Results showed that sapindus saponins improved endothelial response and reduced harmful substances in the hypertensive rats, indicating potential therapeutic benefits for hypertension.
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