21 research outputs found

    Lubiprostone ameliorates the cystic fibrosis mouse intestinal phenotype

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    <p>Abstract</p> <p>Background</p> <p>Cystic fibrosis (CF) is caused by mutations in the <it>CFTR </it>gene that impair the function of CFTR, a cAMP-regulated anion channel. In the small intestine loss of CFTR function creates a dehydrated, acidic luminal environment which is believed to cause an accumulation of mucus, a phenotype characteristic of CF. CF mice have small intestinal bacterial overgrowth, an altered innate immune response, and impaired intestinal transit. We investigated whether lubiprostone, which can activate the CLC2 Cl<sup>- </sup>channel, would improve the intestinal phenotype in CF mice.</p> <p>Methods</p> <p><it>Cftr<sup>tm1UNC </sup></it>(CF) and wildtype (WT) littermate mice on the C57BL/6J background were used. Lubiprostone (10 μg/kg-day) was administered by gavage for two weeks. Mucus accumulation was estimated from crypt lumen widths in periodic acid-Schiff base, Alcian blue stained sections. Luminal bacterial load was measured by qPCR for the bacterial 16<it>S </it>gene. Gastric emptying and small intestinal transit in fasted mice were assessed using gavaged rhodamine dextran. Gene expression was evaluated by Affymetrix Mouse430 2.0 microarray and qRT-PCR.</p> <p>Results</p> <p>Crypt width in control CF mice was 700% that of WT mice (<it>P </it>< 0.001). Lubiprostone did not affect WT crypt width but, unexpectedly, increased CF crypt width 22% (<it>P </it>= 0.001). Lubiprostone increased bacterial load in WT mice to 490% of WT control levels (<it>P </it>= 0.008). Conversely, lubiprostone decreased bacterial overgrowth in CF mice by 60% (<it>P </it>= 0.005). Lubiprostone increased gastric emptying at 20 min postgavage in both WT (<it>P </it>< 0.001) and CF mice (<it>P </it>< 0.001). Lubiprostone enhanced small intestinal transit in WT mice (<it>P </it>= 0.024) but not in CF mice (<it>P </it>= 0.377). Among other innate immune markers, expression of mast cell genes was elevated 4-to 40-fold in the CF intestine as compared to WT, and lubiprostone treatment of CF mice decreased expression to WT control levels.</p> <p>Conclusions</p> <p>These results indicate that lubiprostone has some benefits for the CF intestinal phenotype, especially on bacterial overgrowth and the innate immune response. The unexpected observation of increased mucus accumulation in the crypts of lubiprostone-treated CF mice suggests the possibility that lubiprostone increases mucus secretion.</p

    Immunological mechanism of action and clinical profile of disease-modifying treatments in multiple sclerosis.

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    Multiple sclerosis (MS) is a life-long, potentially debilitating disease of the central nervous system (CNS). MS is considered to be an immune-mediated disease, and the presence of autoreactive peripheral lymphocytes in CNS compartments is believed to be critical in the process of demyelination and tissue damage in MS. Although MS is not currently a curable disease, several disease-modifying therapies (DMTs) are now available, or are in development. These DMTs are all thought to primarily suppress autoimmune activity within the CNS. Each therapy has its own mechanism of action (MoA) and, as a consequence, each has a different efficacy and safety profile. Neurologists can now select therapies on a more individual, patient-tailored basis, with the aim of maximizing potential for long-term efficacy without interruptions in treatment. The MoA and clinical profile of MS therapies are important considerations when making that choice or when switching therapies due to suboptimal disease response. This article therefore reviews the known and putative immunological MoAs alongside a summary of the clinical profile of therapies approved for relapsing forms of MS, and those in late-stage development, based on published data from pivotal randomized, controlled trials

    Immunological Mechanism of Action and Clinical Profile of Disease-Modifying Treatments in Multiple Sclerosis

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    Research on the Micro-blog User Behavior Model Based on Behavior Matrix

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    Part 6: Intelligent RobotInternational audienceThe micro-blog user behavior model based on behavior matrix is proposed based on the analysis of the current related researches. In the proposed method, two behavior matrices named original behavior matrix and individual behavior matrix are constructed; And then, the analysis method of behavior matrix is utilized to mine the representative behaviors, which can reflect the disciplines of the user; Finally, the experiments on the 2043 blogs of 9 users from June 15, 2016 to August 1, 2016 reflect the individual behavior disciplines

    Social media and healthcare : an overview

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    In our "e-society," social media are pervasive, rapidly evolving, and increasingly influencing the health care landscape. In fact, it is becoming more important that all health care providers understand the basic function of social media processes including what they are, who uses them, what they can be used for, and how they might affect one's practice. Social media are now integrated in many individuals' daily routines, and there is no question that social media are changing the way patients communicate with each other. For example, patients compare notes on support groups, new investigations, treatments, and even physicians and thus continue to take an active role in their health care [1]. With the continued growth of social media, physicians in practice and health care delivery organizations must understand this phenomenon and how it may be used in a positive way to connect with patients. It is beyond the scope of this article to explore in detail the types, uses, and impact of social media, but the authors will present a brief overview that covers the basics of how social media are being used in health care and beyond
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