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First person – Karishma Chhabria

机译:第一人称视角– Karishma Chhabria

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First Person is a series of interviews with the first authors of a selection of papers published in Disease Models & Mechanisms (DMM), helping early-career researchers promote themselves alongside their papers. Karishma Chhabria is first author on ‘ Sodium nitroprusside prevents the detrimental effects of glucose on the neurovascular unit and behaviour in zebrafish ’, published in DMM. Karishma conducted the research described in this article while a PhD student in Tim Chico and Clare Howarth's lab at University of Sheffield, UK. She is now a postdoc in the lab of David Kleinfeld at UCSD, USA, investigating how the brain achieves precise spatio-temporal blood-flow regulation. Karishma Chhabria How would you explain the main findings of your paper to non-scientific family and friends? Diabetes affects around 1 in 11 of the world's adult population and poses a risk for both heart and brain diseases. A common feature of type 2 diabetes is high blood-glucose levels. In our study, we investigate the effect of feeding high glucose to zebrafish on brain function and behavior. We find that high-glucose-fed zebrafish have several abnormities in various cells in the brain and also display abnormal behavior. Intriguingly, we observed that all the negative effects of high-glucose exposure on the brain and behavior can be treated with a drug that artificially increases nitric oxide in the brain. It has commonly been shown that there is a deficiency of nitric oxide in the brain under diabetes; however, there are no existing nitric-oxide-based therapeutic treatments for diabetes. Our study shows for the first time that nitric-oxide donors could be used as potential therapeutics to treat diabetes and related brain dysfunctions. “Our study shows for the first time that nitric-oxide donors could be used as potential therapeutics to treat diabetes and related brain dysfunctions.” What are the potential implications of these results for your field of research? The human brain is energetically expensive, consuming around 20% of the cardiac output while accounting for only 2% of the body weight. Neurons don't have their own energy reserves and therefore rely on a continuous supply of blood flow to receive the oxygen and glucose needed for their survival. The matching of this energy supply and demand is achieved through a phenomenon called neurovascular coupling. There has been a recent increase in research investigating the importance of neurovascular coupling in disease; however, the precise mechanisms are not known. In our earlier paper, we showed that high-glucose exposure impairs neurovascular coupling and in the current study we have shown dysfunction of the critical cells known to mediate neurovascular coupling. Our current study applies multiscale research methodologies, showing high-glucose-induced dysfunctions from the cellular level through to behavior. What are the main advantages and drawbacks of the model system you have used as it relates to the disease you are investigating? The biggest advantage of using larval zebrafish as a model system for investigating disease is the ease of screening several prospective drugs for various diseases. Larval zebrafish at 8?days post-fertilization are capable of performing complex visual tasks like object preference, thus presenting the ability to also investigate mechanisms of behavioral dysfunctions. Additional advantages are the ease of manipulating genes and the optical transparency of the larval forms. In our current study, we have investigated the effect of high-glucose exposure, a pathology of diabetes. However, to understand the disease in its entirety, development of a larval zebrafish model of diabetes would be ideal. Although streptozotocin-induced diabetes models exist, these are more commonly available in adult zebrafish. The ability to image neurovascular function in adult zebrafish using state-of-the-art lightsheet microscopy would be a step forward, allowing us to more fully investigate the pathological consequences of diseases. “The biggest advantage of using larval zebrafish as a model system for investigating disease is the ease of screening several prospective drugs for various diseases.” What has surprised you the most while conducting your research? There are two main aspects of my research that I found particularly striking, including our observations of neuronal hyperexcitability and TRPV4 underexpression induced by glucose exposure. Secondly, I was surprised by the large effect of the nitric-oxide donor in reversing all the detrimental effects of the high-glucose exposure. This could have immense potential for investigating novel nitric-oxide-based therapeutics to treat diabetes and related brain dysfunction.
机译:《第一人称》是对一系列发表在《疾病模型与机制》(DMM)上的论文的第一作者的一系列采访,有助于早期职业研究人员与他们的论文一起发展自我。 Karishma Chhabria是DMM上发表的“硝普钠预防葡萄糖对斑马鱼神经血管单位和行为的有害影响”的第一作者。 Karishma是在Tim Sheco和英国Sheffield大学的Clare Howarth实验室的博士研究生期间进行本文所述的研究的。她现在是美国UCSD的David Kleinfeld实验室的博士后,研究大脑如何实现精确的时空血流调节。 Karishma Chhabria您将如何向非科学的家人和朋友解释论文的主要发现?糖尿病影响着全世界约11个成年人口中的1个,并有患心脏病和脑部疾病的风险。 2型糖尿病的一个共同特征是血糖水平高。在我们的研究中,我们调查了向斑马鱼喂食高葡萄糖对脑功能和行为的影响。我们发现,高糖喂养的斑马鱼在大脑的各个细胞中都有一些异常,并且还表现出异常行为。有趣的是,我们观察到,高糖暴露对大脑和行为的所有负面影响都可以通过人工增加大脑中一氧化氮的药物来治疗。普遍表明,糖尿病患者的大脑中缺乏一氧化氮。但是,目前没有基于一氧化氮的糖尿病治疗方法。我们的研究首次表明,一氧化氮供体可以用作治疗糖尿病和相关脑功能障碍的潜在疗法。 “我们的研究首次表明,一氧化氮供体可以用作治疗糖尿病和相关脑功能障碍的潜在疗法。”这些结果对您的研究领域有何潜在影响?人脑在能量上非常昂贵,消耗约20%的心输出量,而仅占体重的2%。神经元没有自己的能量储备,因此依赖于持续不断的血流供应来获得生存所需的氧气和葡萄糖。这种能量供需的匹配是通过称为神经血管耦合的现象实现的。研究神经血管偶联在疾病中的重要性的研究近来有所增加。但是,确切的机制尚不清楚。在我们较早的论文中,我们表明高糖暴露会损害神经血管耦合,而在当前研究中,我们已经显示了已知的介导神经血管耦合的关键细胞功能异常。我们当前的研究应用了多尺度研究方法,显示了从细胞水平到行为的高糖诱导的功能障碍。您所使用的模型系统与要研究的疾病相关的主要优缺点是什么?使用幼虫斑马鱼作为研究疾病的模型系统的最大优点是易于筛查各种疾病的几种前瞻性药物。受精后第8天的幼虫斑马鱼能够执行复杂的视觉任务,例如对象偏爱,因此具有研究行为异常机制的能力。其他优点是操作基因的简便性和幼虫形式的光学透明性。在我们目前的研究中,我们研究了高糖暴露(一种糖尿病病理)的作用。但是,要全面了解该疾病,开发幼虫斑马鱼糖尿病模型非常理想。尽管存在链脲佐菌素诱导的糖尿病模型,但在成年斑马鱼中更常见。使用最新的光片显微镜在成年斑马鱼中成像神经血管功能的能力将向前迈出一步,使我们能够更充分地研究疾病的病理后果。 “使用幼虫斑马鱼作为研究疾病的模型系统的最大优势是易于筛查多种前瞻性药物来治疗各种疾病。”在进行研究时,给您最大的惊喜是什么?我的研究有两个主要方面,我特别引人注目,包括我们对葡萄糖暴露引起的神经元过度兴奋和TRPV4表达不足的观察。其次,我惊讶于一氧化氮供体在逆转高葡萄糖暴露的所有有害作用方面的巨大作用。这可能有巨大的潜力来研究新型的基于一氧化氮的疗法来治疗糖尿病和相关的脑功能障碍。

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