Publications by authors named "Bi-Lin Lin"

Meningeal metastasis (LM) is commonly seen in the advanced stages of cancer patients, often leading to a rapid decline in survival time and quality of life. Currently, there is still a lack of standardized treatments. Oncolytic viruses (OVs) are a class of emerging cancer therapeutics with the advantages of selectively replicating in cancer cells, delivering various eukaryotic transgenes, inducing immunogenic cell death, and promoting anti-tumor immunity.

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The ventral subiculum (vSUB), the major output structure of the hippocampal formation, regulates motivation, stress integration, and anxiety-like behaviors that rely on heightened arousal. However, the roles and underlying neural circuits of the vSUB in wakefulness are poorly known. Using in vivo fiber photometry and multichannel electrophysiological recordings in mice, we found that the vSUB glutamatergic neurons exhibited high activities during wakefulness.

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Two previously undescribed cholestanol saponins, parpetiosides F - G (1-2), and six known analogs (3-8) were isolated from the rhizomes of Paris fargesii var. petiolata. Their structures were elucidated by extensive spectroscopic data analysis and chemical methods.

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Article Synopsis
  • The study focuses on Paris polyphylla var. yunnanensis, a plant used in traditional Chinese medicine, aiming to isolate and identify its bioactive saponins.
  • Researchers identified fourteen saponins, including seven new compounds, with Paris saponins VII (PSVII) exhibiting strong cytotoxicity against a specific pancreatic cancer cell line (BxPC-3) at low concentrations.
  • Further analysis indicated that PSVII could inhibit cell growth and promote cell death through mechanisms involving apoptosis and pyroptosis by activating specific caspases.
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  • * The study highlights the role of parvalbumin (PV) neuronal networks and neuregulin 1-ErbB4 signaling in the mPFC’s plasticity and fear extinction in adult male mice.
  • * Findings suggest that the configuration of these PV networks influences how certain neurons regulate fear extinction, opening up potential new therapies for fear disorders.
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The posttraumatic stress disorder is marked by an impaired ability to extinct fear memory acquired in trauma. Although previous studies suggest that fear extinction depends on the function of the amygdala, the underlying mechanisms are unclear. We found that NRG1 receptors (ErbB4) were abundantly expressed in the intercalated cells mass of amygdala (ITC).

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The dysregulation of fear learning and abnormal activities of cerebral networks may contribute to the etiologies of anxiety disorders. Although it has been proposed that decreased activity in the paraventricular nucleus of the thalamus (PVT) to the lateral central nucleus of amygdala (CeL) pathway could induce an attenuation of learned fear, no study has shown the effect of the direct optogenetic activation of PVT projecting CeL neurons in vivo on unconditioned fear-related behaviors or learned fear expression. The mechanisms that control the neuronal activity of the PVT-CeL pathway involved in anxiety are rare.

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Gallic acid (GA) is a polyphenolic natural product widely distributed in food, beverage, and traditional Chinese herbs with beneficial effects on the cardiovascular system. In this research, a comparative study was conducted to investigate the possible difference of pharmacokinetic process in normal and isoproterenol-induced myocardial infarcted rats after oral administration of GA monohydrate with the dose of 50 and 100 mg/kg, respectively. Quantification of GA in rat plasma was achieved by using a simple and rapid high-performance liquid chromatographic method.

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An abnormal neuronal activity in the amygdala is involved in the pathogenesis of anxiety disorders. However, little is known about the mechanisms. High-anxiety mice and low-anxiety mice, representing the innate extremes of anxiety-related behaviors, were first grouped according to their anxiety levels in the elevated plus maze test.

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Article Synopsis
  • Anxiety disorders are linked to various psychiatric diseases, and the hippocampus plays a key role in managing anxiety.
  • Research found that the expression of Endothelin-1 (ET1) is reduced in high-anxiety mice, and blocking ET1 leads to increased anxiety behaviors.
  • ET1 signaling is crucial for regulating the activity of certain neurons in the hippocampus, suggesting that it could influence anxiety levels and potentially help explain emotional issues stemming from ischemic stroke.
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The bed nucleus of the stria terminalis (BNST), a nucleus defined as part of the extended amygdala, is involved in the expression of anxiety disorders. However, the regulatory mechanisms of BNST inhibitory activity that is involved in anxiety are unknown. Here, we showed that blocking neuregulin 1 (NRG1)-ErbB4 signaling in the BNST of mice, by either neutralizing endogenous NRG1 with ecto-Erbb4 or antagonizing the ErbB4 receptor with its specific inhibitor, produced anxiogenic responses.

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Apoptosis plays a critical role in tumorigenesis. TP63 inhibits the pro-apoptosis function of TP53, and CD40 increases expression of anti-apoptotic proteins. Two single nucleotide polymorphisms (SNPs), rs6790167 (g243059A>G) in intron 9 of TP63 and rs1535045 (g6194C>T) in intron 1 of CD40 respectively, may affect the susceptibility of lung cancer.

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Endothelin1 (ET1) is a potent vasoconstrictor that is also known to be a neuropeptide that is involved in neural circuits. We examined the role of ET1 that has been implicated in the anxiogenic process. We found that infusing ET1 into the IL cortex increased anxiety-like behaviors.

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Article Synopsis
  • - The study explores how inhibitory neurotransmission in the amygdala is vital for fear learning and memory, focusing on the role of neuregulin 1 (NRG1) and its receptor ErbB4 in controlling GABAergic activity.
  • - It was found that disabling NRG1 or removing ErbB4 led to reduced GABA transmission and impaired fear conditioning, particularly when ErbB4 was absent in specific neurons.
  • - The research suggests that NRG1 signaling is crucial for maintaining GABA activity in the amygdala, linking these findings to potential mechanisms for schizophrenia since both NRG1 and ErbB4 are implicated in this disorder.
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Embryoid bodies (EBs) with large starting numbers of embryonic stem cells (ESCs) have a greater degree of cardiac differentiation than from low numbers of EBs. However, the biological roles of signaling molecules in these effects are not well understood. Here, we show that groups of EBs with different starting numbers of ESCs had differential gene expression patterns for Wnt5a and Wnt11.

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Anxiety disorder is related to the pathophysiology of psychiatric diseases, including major depression, substance abuse, and schizophrenia. The amygdala is important for manifestation and modulation of anxiety. However, relatively little is known regarding the mechanisms that control the amygdala inhibitory activity that is involved in anxiety.

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  • The medial prefrontal cortex (mPFC) is important for controlling anxiety, but it's not clear how certain chemical signals in a specific part of it (the infralimbic or IL cortex) affect anxiety behaviors.
  • Experiments showed that activating the IL cortex made mice less likely to explore and more anxious, while turning it off made them less anxious.
  • Differences in brain activity were found between anxious and less anxious mice, suggesting that an imbalance in chemical signals might be a reason why some mice experience more anxiety than others.
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Neuregulin-1β (NRG-1β)/ErbB signaling plays crucial roles in the cardiac differentiation of mouse embryonic stem cells (ESCs), but its roles and the underlying mechanisms in cardiac differentiation are incompletely understood. This study showed that NRG-1β significantly increased the percentage of beating embryoid bodies (EBs) and up-regulated the gene expressions of Nkx2.5, GATA4, α-actin, MLC-2v, and ANF in a time-dependent manner, with no effect on the gene expressions of HCN4 and Tbx3.

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The traditional Chinese medicine bufalin, extracted from toad's skin, has been demonstrated to exert anticancer activities in various kinds of human cancers. The mechanisms of action lie in its capacity to induce apoptosis, or termed type I programmed cell death (PCD). However, type II PCD, or autophagy, participates in cancer proliferation, progression, and relapse, as well.

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Background: Traditional Chinese medicinal herbs Cortex Moutan and Radix Salviae Milthiorrhizaeare are prescribed together for their putative cardioprotective effects in clinical practice. However, the rationale of the combined use remains unclear. The present study was designed to investigate the cardioprotective effects of paeonol and danshensu (representative active ingredient of Cortex Moutan and Radix Salviae Milthiorrhizae, respectively) on isoproterenol-induced myocardial infarction in rats and its underlying mechanisms.

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An analysis method was developed to determine the chemical speciation of Cu, Zn, Fe and Mn in radix scutellariae decoction using atomic absorption spectroscopy(AAS). The decoction can be divided into suspension and soluble species by 0.45 microm filter membrane and the soluble species can be separated into organism and inorganic species by LSA-10 macroporous resin.

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  • - Ropinirole is a medication effective for treating idiopathic Parkinson's disease and the study aimed to investigate how another drug, Madopar, affects its absorption in healthy Chinese volunteers.
  • - In a randomized crossover study, 12 participants received 1 mg of ropinirole orally after taking either a placebo or Madopar, and their pharmacokinetic parameters were measured.
  • - The results showed that coadministering ropinirole with Madopar did not significantly alter its availability or other pharmacokinetic parameters, suggesting no need to adjust ropinirole dosage in combination with Madopar for Chinese patients.
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