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Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2019-09-01 DOI: 10.1002/cptx.63
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引用次数: 0
Assembly and Application of a Three‐Dimensional Human Corneal Tissue Model 三维人体角膜组织模型的组装与应用
Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2019-09-01 DOI: 10.1002/cptx.84
Tina B McKay, Andrew Ford, Siran Wang, Dana M. Cairns, Rachael N. Parker, Phillip M. Deardorff, C. Ghezzi, D. Kaplan
The cornea provides a functional barrier separating the outside environment from the intraocular environment, thereby protecting posterior segments of the eye from infection and damage. Pathological changes that compromise the structure or integrity of the cornea may occur as a result of injury or disease and can lead to debilitating effects on visual acuity. Over 10 million people worldwide are visually impaired or blind due to corneal opacity. Thus, physiologically relevant in vitro approaches to predict corneal toxicity of chemicals or effective treatments for disease prior to ocular exposure, as well as to study the corneal effects of systemic, chronic conditions, such as diabetes, are needed to reduce use of animal testing and accelerate therapeutic development. We have previously bioengineered an innervated corneal tissue model using silk protein scaffolds to recapitulate the structural and mechanical elements of the anterior cornea and to model the functional aspects of corneal sensation with the inclusion of epithelial, stromal, and neural components. The purpose of this unit is to provide a step‐by‐step guide for preparation, assembly, and application of this three‐dimensional corneal tissue system to enable the study of corneal tissue biology. © 2019 by John Wiley & Sons, Inc.
角膜提供了将外部环境与眼内环境分离的功能屏障,从而保护眼睛后部免受感染和损伤。损伤或疾病可能会导致损害角膜结构或完整性的病理变化,并可能导致视力下降。全世界有1000多万人因角膜混浊而视力受损或失明。因此,需要采用生理相关的体外方法来预测化学物质的角膜毒性或在眼睛暴露前对疾病的有效治疗,以及研究全身慢性疾病(如糖尿病)的角膜影响,以减少动物试验的使用并加速治疗发展。我们之前已经使用丝蛋白支架对神经支配的角膜组织模型进行了生物工程,以概括前角膜的结构和机械元件,并通过包括上皮、基质和神经成分来对角膜感觉的功能方面进行建模。本单元的目的是为这种三维角膜组织系统的制备、组装和应用提供一个循序渐进的指南,以实现角膜组织生物学的研究。©2019 John Wiley&Sons,股份有限公司版权所有。
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引用次数: 9
Assessment of Sertoli Cell Proliferation by 3‐(4,5‐Dimethylthiazol‐2‐yl)‐2,5‐Diphenyltetrazolium Bromide and Sulforhodamine B Assays 用3‐(4,5‐二甲基噻唑‐2‐基)‐2,5‐二苯基溴化四唑和硫代丹明B试验评估支持细胞增殖
Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2019-09-01 DOI: 10.1002/cptx.85
A. Martins, P. Oliveira, Marco G. Alves
The correct functioning of Sertoli cells (SCs) is pivotal for successful spermatogenesis. They are major targets for hormones, endocrine disruptors, and other substances that men are subjected to every day. One of the main SC functions that quickly responds to a deleterious stimulus is proliferation. This is directly related to the in vivo capacity of these cells to sustain a good number of developing germ cells. The protocols in this article can be tested on SCs of different origin. For the case of human SCs from small human testicular biopsies, a short and simple protocol to isolate and culture these cells is provided. The other protocols discussed herein represent two different procedures, somewhat complementary, to assess SC proliferation. In brief, the sulforhodamine B assay allows the investigator to dye healthy fixed SCs maintained in culture. In the MTT assay, on the other hand, 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide (MTT) is reduced by live SCs. These methods are mostly used to evaluate how SC proliferative activity responds to exposure to compounds such as toxicants or hormones. © 2019 by John Wiley & Sons, Inc.
支持细胞(SCs)的正常功能对精子的成功发生至关重要。它们是激素、内分泌干扰物和其他男性每天都要承受的物质的主要目标。快速响应有害刺激的主要SC功能之一是增殖。这直接关系到这些细胞在体内维持大量发育中的生殖细胞的能力。本文中的协议可以在不同来源的SCs上进行测试。对于从人类小睾丸活检中提取的人类SCs,提供了一种简短而简单的分离和培养这些细胞的方案。本文讨论的其他方案代表了两种不同的程序,有些互补,以评估SC增殖。简而言之,硫磺胺B检测允许研究者对培养中维持的健康固定SCs进行染色。另一方面,在MTT试验中,3‐(4,5‐二甲基噻唑‐2‐基)‐2,5‐二苯基溴化四唑(MTT)被活SCs还原。这些方法主要用于评估SC的增殖活性对暴露于诸如毒物或激素等化合物的反应。©2019 by John Wiley & Sons, Inc。
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引用次数: 2
Toxicokinetics 毒性动力学
Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2009-08-01 DOI: 10.1002/0471140856.tx0500s41
I. G. Sipes, E. Hodgson
T oxicokinetics is a specialized area of toxicology that blends pharmacokinetic procedures with those of toxicology. It involves understanding the processes that govern the absorption, distribution, metabolism, and excretion of chemicals by the body. In general, these processes can be referred to as input (absorption), translocation (distribution), and output (metabolism, excretion). The rates of each process can be derived and used to describe in mathematical terms the time course for chemical and metabolite disposition in the body. Each process is governed by a number of physicochemical, biochemical, and physiological factors that profoundly affect how the body handles a particular chemical. For example, the state of hydration of the skin is an important physicochemical factor that influences chemical absorption by that route. Also, metabolic enzymes can have a profound effect on the input and output processes for a chemical. Thus, factors that increase the rate of biotransformation (enzymatic metabolism) of a chemical can profoundly affect input (increased formation of a toxic metabolite) or output (increased detoxification) processes that govern the temporal patterns of response to a particular chemical. These factors include induction and/or inhibition of xenobiotic-metabolizing enzymes, and inter-individual variations may result from the presence of polymorphisms in these enzymes. Reduction of adipose tissue mass reduces a storage compartment for lipophilic chemicals and thus can alter their rate of elimination from the body. Since toxicants are frequently present as complex mixtures, the way in which one toxicant can affect the toxicokinetics of another is important and will be considered in subsequent units.
氧代动力学是毒理学的一个专门领域,它将药代动力学程序与毒理学程序相结合。它包括对人体化学物质的吸收、分布、代谢和排泄过程的理解。一般来说,这些过程可以被称为输入(吸收)、易位(分布)和输出(代谢、排泄)。每个过程的速率可以推导出来,并用数学术语来描述体内化学和代谢物处置的时间过程。每个过程都受到许多物理化学、生物化学和生理因素的控制,这些因素深刻地影响着身体如何处理特定的化学物质。例如,皮肤的水合状态是一个重要的物理化学因素,影响通过该途径吸收化学物质。此外,代谢酶可以对化学物质的输入和输出过程产生深远的影响。因此,增加化学物质生物转化速率(酶代谢)的因素可以深刻地影响输入(有毒代谢物的形成增加)或输出(解毒增加)过程,这些过程控制对特定化学物质的反应的时间模式。这些因素包括诱导和/或抑制外源代谢酶,而这些酶的多态性可能导致个体间的差异。脂肪组织质量的减少减少了亲脂性化学物质的储存空间,因此可以改变它们从体内消除的速度。由于毒物经常以复杂混合物的形式出现,一种毒物如何影响另一种毒物的毒性动力学是很重要的,将在随后的单元中加以考虑。
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引用次数: 0
Immunotoxicology 免疫毒理学
Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 1987-01-01 DOI: 10.1007/978-94-009-4307-0
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引用次数: 0
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Current protocols in toxicology / editorial board, Mahin D. Maines (editor-in-chief) ... [et al.]
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