综述与专论: 蝙蝠，听觉和回声定位研究的模型动物

科学家以蝙蝠为模式动物,从听觉、回声定位和生态适应与演化等方面开展了研究,取得了令人瞩目的成果。为适应回声定位,蝙蝠听觉系统的结构和功能产生了明显的特化。从外周到中枢形成了对声频率极为有序的表征,甚至在恒频-调频（constant frequency-frequency modulation,CF-FM）蝙蝠耳蜗形成了所谓的听觉凹,以及听皮质功能组构也模块化,成为了具有代表性的特化象征。神经元反应的潜伏期对蝙蝠不仅是基本特性,也是回声定位行为调控的一部分;研究发现,有较长潜伏期的神经元具有较尖锐的回声-延迟调谐特性,而较短潜伏期的神经元则有较宽的回声-延迟调谐特性。蝙蝠听神经元对频率调谐的精准度亦远胜于人类和其他非回声定位动物;而且,源于耳蜗听觉凹的传入在各级听中枢均显示出对回声定位信号第二谐波CF成分的过度表征,以满足对靶物回声多普勒频移探测的需要。时程是回声定位蝙蝠发声信号主动改变的参数之一,而时程调谐神经元则提供了一种编码声音时相特征的重要神经机制,匹配了对回声定位信号时相信息加工的需要。在多种回声定位蝙蝠的听中枢还发现,有回声-延迟调谐神经元,它们不仅能对靶物距离进行调谐,而且...     

CF-FM蝙蝠听中枢神经元处理行为相关声信号的神经机制

蝙蝠具有高度发达的回声定位系统,能够准确地处理和整合不断变化环境中的声学参数,以保持最佳的生理和行为状态。这种行为的神经生理机制已经得到了广泛的研究。本文主要探究了CF-FM蝙蝠听觉中枢处理种属特异性声信号、共变参数、多普勒频移补偿信号及多谐波声信号的神经机制,可有助于了解回声定位蝙蝠处理行为相关声信号的神经策略。同时本文也提出将来可以CF-FM蝙蝠作为模式动物进行更深入的胞内研究。     

马铁菊头蝠对同种咀嚼声的反应研究

咀嚼是哺乳动物食物吸收的重要组成部分,对动物的生存和繁殖极其重要。动物咀嚼时会发出低频低强度的咀嚼声,研究表明人类的咀嚼声可以增强自身或他人的食欲和愉悦度。蝙蝠作为哺乳动物中的第二大类群,其咀嚼声的特征和功能仍不清楚。本研究以吉林省集安市治安村的马铁菊头蝠Rhinolophus ferrumequinum为研究对象,通过回放蝙蝠咀嚼声和空白对照实验,同步录制蝙蝠的进食行为和回声定位声波,试图阐明蝙蝠咀嚼声对其进食行为和回声定位声波的影响。结果表明:进食次数在2种回放条件下的差异无统计学意义,但捕食尝试在2种回放条件下的差异有统计学意义。因此,咀嚼声能够显著地提高蝙蝠的进食欲望。此外,在蝙蝠咀嚼声的刺激下,其回声定位声波的频率增加,持续时间延长,脉冲速率减慢。这可能是因为蝙蝠在咀嚼声的影响下改变发声动机,从而改变了其回声定位声波的频谱时间结构。本研究第一次报道了蝙蝠咀嚼声对其进食行为的影响,为进一步阐明蝙蝠咀嚼声的功能和进化具有重要意义。     

翼手目(蝙蝠)适应性进化分子机制的研究进展

作为哺乳动物第二大目的翼手目(Chiroptera;俗称蝙蝠)在飞行能力、回声定位与听觉系统、食性、冬眠、免疫防御等诸多方面表现出显著而独特的适应性进化,是研究生物对环境适应性进化分子机制的热点模型之一。文章综述了翼手目适应性进化分子机制的研究进展,特别是近年来在基因组水平上开展的相关研究,显示出更为复杂的分子进化模式和功能分化。随着越来越多的翼手目物种基因组数据的产生,将有望揭示新的进化机制,并为后续的功能实验奠定基础,促进人们对翼手目这一类群的认识和了解,同时也为系统认识动物适应性进化分子机制做出贡献。     

高度杂波空间中 CF-FM 蝙蝠下丘回声定位的神经机制

蝙蝠是回声定位的专家。对于在高度杂波空间中捕食的CF-FM蝙蝠,面临着如何从发声和众多由背景环境物体反射的杂波回声中分辨和判断来自靶物的回声所携带信息的问题。已有研究表明,CF-FM蝙蝠可通过发出复杂成分的声脉冲,并通过听中枢的时相和频率整合来处理杂波环境下发声-回声对中包含的靶物距离和相对移动速度的信息。就以上方面在听中脑下丘的神经机制进行概述,以促进人们对听中枢在复杂听环境下对回声定位信号加工原理的认识。     

蝙蝠与超声波、回声定位(1)

回声定位是高度演化、极为复杂的过程,使蝙蝠可利用大多数动物不能利用的生态位——漆黑的洞穴和黑夜的天空。对蝙蝠的回声定位研究已有近80年的历史,科学家已经从生物声学层面基本了解和认识了蝙蝠回声定位的特征、机制、生物学意义等,关于分子和神经生物学方面的机制也得到深入研究。重点介绍蝙蝠回声定位的研究历史,以及蝙蝠的超声波和回声定位在生物学和声学层面的基础知识。     

蝙蝠声音信号功能研究进展

声音信号介导动物的资源竞争、配偶选择及反捕食等系列生活史事件,对维持动物种群稳定与群落平衡至关重要。蝙蝠占据夜空生态位,视觉退化,听觉发达,一直被视为声学研究的模式生物。本文围绕蝙蝠回声定位声波与交流声波的功能,综述当前研究现状,展望未来发展方向。纵观已有研究,蝙蝠回声定位声波具有多重功能,包括空间导航与猎物探测、水体与植被识别、协调觅食活动及传递交流信息。蝙蝠利用交流声波从事社群活动,包括社群联系、资源防御、繁殖活动及求救呼叫。绝大多数研究关注蝙蝠回声定位声波的功能,有关蝙蝠交流声波的功能近年才引起重视。未来工作有待进一步探究蝙蝠声音信号产生的影响机制。     

听觉中枢神经元对声信号的识别和处理

人类听觉的基本特性和机制与其他哺乳动物相似,因此,利用动物所作的听觉研究和获得的结果,有助于认识人类自身的听觉.围绕听觉中枢神经元对不同模式的声信号的识别和处理,简要综述了这方面的研究.声信号和声模式识别在听觉中枢对声信号的感受和加工中具有重要意义.听神经元作为声模式识别的结构和功能基础,对不同的声刺激模式产生不同反应,甚至是在同一声刺激模式下,改变其中的某个声参数,神经元的反应也会发生相应改变,而其反应的特性和机制均需要更多研究来解答.另外,声信号作为声信息的载体,不同的声信息寓于不同的声参数和声特征之中,研究发现,听觉中枢神经元存在相应的声信息甄别和选择的神经基础,能对动态变化的声频率、幅度和时程等进行反应和编码,并且,在不同种类动物上获得的研究结果极为相似,表明听觉中枢对不同声信号和声刺激模式的识别、分析和加工,具有共同性和普遍性.     

马铁菊头蝠不同行为下的回声定位叫声

蝙蝠回声定位的研究自50年代以来在世界范围内经久不衰,从行为生态学及神经生物学两方面研究回声定位又是该领域最近十几年的热点.其中从行为生态学角度主要研究蝙蝠回声定位对其所处生境及捕食行为的适应性;神经生物学则研究蝙蝠通过回声定位而"观察"周围世界的神经生理学基础.相比之下我国对蝙蝠的回声定位行为研究较少,孙心德等对鲁氏菊头蝠(Rhinolophus rouxi)进行过回避障碍物及听觉神经机理的研究,而对于蝙蝠回声定位超声波信号的研究则基本是空白.     

东方蝙蝠在交通噪声环境中的回声定位行为

环境噪声会降低动物声信号可探测性,是动物声信号进化的压力。为了避免人工噪声干扰,多数脊椎动物调整其叫声的频谱-时间结构,如采用延长叫声持续时间、提高频率和增加强度等策略。本研究选择回声定位声波频率范围与交通噪声频率范围相互重叠的东方蝙蝠(Vespertilio sinensis)为研究对象,在自然条件下开展实验,研究交通噪声对蝙蝠回声定位声波的影响。本实验选择交通噪声强度存在差异的两个样点,分别录制东方蝙蝠的回声定位声波,分析其结构参数。在交通噪声强度较高的样点,东方蝙蝠回声定位声波的持续时间、斜率均未显著改变,但起始频率、主频、终止频率及带宽均显著提高。结果表明,东方蝙蝠的回声定位行为在交通噪声干扰下具有明显的可塑性。     

Recent advances in the study of Kaposi's sarcoma-associated herpesvirus replication and pathogenesis

It has now been over twenty years since a novel herpesviral genome was identified in Kaposi's sarcoma biopsies. Since then, the cumulative research effort by molecular biologists, virologists, clinicians, and epidemiologists alike has led to the extensive characterization of this tumor virus, Kaposi's sarcoma-associated herpesvirus(KSHV; also known as human herpesvirus 8(HHV-8)), and its associated diseases. Here we review the current knowledge of KSHV biology and pathogenesis, with a particular emphasis on new and exciting advances in the field of epigenetics. We also discuss the development and practicality of various cell culture and animal model systems to study KSHV replication and pathogenesis.     

A Unique Protease Cleavage Site Predicted in the Spike Protein of the Novel Pneumonia Coronavirus (2019-nCoV) Potentially Related to Viral Transmissibility

正Dear Editor,In December 2019, a novel human coronavirus caused an epidemic of severe pneumonia(Coronavirus Disease 2019,COVID-19) in Wuhan, Hubei, China(Wu et al. 2020; Zhu et al. 2020). So far, this virus has spread to all areas of China and even to other countries. The epidemic has caused 67,102 confirmed infections with 1526 fatal cases     

Curcuminoids as inhibitors of thioredoxin reductase: A receptor based pharmacophore study with distance mapping of the active site

Curcumin is the yellow pigment of turmeric that interacts irreversibly forming an adduct with thioredoxin reductase (TrxR), an enzyme responsible for redox control of cell and defence against oxidative stress. Docking at both the active sites of TrxR was performed to compare the potency of three naturally occurring curcuminoids, namely curcumin, demethoxy curcumin and bis-demethoxy curcumin. Results show that active sites of TrxR occur at the junction of E and F chains. Volume and area of both cavities is predicted. It has been concluded by distance mapping of the most active conformations that Se atom of catalytic residue SeCYS498, is at a distance of 3.56 from C13 of demethoxy curcumin at the E chain active site, whereas C13 carbon atom forms adduct with Se atom of SeCys 498. We report that at least one methoxy group in curcuminoids is necessary for interation with catalytic residues of thioredoxin. Pharmacophore of both active sites of the TrxR receptor for curcumin and demethoxy curcumin molecules has been drawn and proposed for design and synthesis of most probable potent antiproliferative synthetic drugs.     

Synthesis and antimicrobial studies of hydrazone derivatives of 4-[3-(2,4-difluorophenyl)-4-formyl-1H-pyrazol-1-yl]benzoic acid and 4-[3-(3,4-difluorophenyl)-4-formyl-1H-pyrazol-1-yl]benzoic acid

Microbial resistance to antibiotics is an unresolved global concern, which needs urgent and coordinated action. One of the guidelines of the Centers for Disease Control and Preventions (CDC) to combat antibiotic resistance is the development of new antibiotics to treat drug-resistant bacteria. In our effort to find new antibiotics, we report the synthesis and antimicrobial studies of 30 new pyrazole derivatives. These novel molecules have been synthesized by using readily available starting materials and benign reaction conditions. Some of these molecules have shown activity with MIC values as low as 0.78?µg/mL against four bacterial strains; Staphylococcus aureus, methicillin-resistant S. aureus, Bacillus subtilis, and Acinetobacter baumannii. Furthermore, active molecules are non-toxic to mammalian cell line.

     

Comparative morphology of the carpel in the Liliaceae: Hewardieae, Petrosavieae, and Tricyrteae

The young pistils in the melanthioid tribes, Hewardieae, Petrosavieae and Tricyrteae, are uniformly tricarpellate and syncarpous. They lack raphide idioblasts. All are multiovulate, with bitegmic ovules. The Petrosavieae are marked by the presence of septal glands and incomplete syncarpy. Tepals and stamens adhere to the ovary in the Hewardieae and the Petrosavieae but not in the Tricyrteae. Two vascular bundles occur in the stamens of the Hewartlieae and Tricyrtis latifolia. Ventral bundles in the upper part of the ovary of the Hewardieae are continuous with compound septal bundles and placental bundles in the lower part. Putative ventral bundles occur in the alternate position in the Tricyrteae and putative placental bundles in the opposite. position in the Petrosavieae. The dichtomously branched stigma in each carpel of the Tricyrteae is supplied by a bifurcated dorsal bundle.     

Novel compounds with potent CDK9 inhibitory activity for the treatment of myeloma

Cyclin-dependent kinases (CDKs) and Polo-like kinases (PLKs) play key role in the regulation of the cell cycle. The aim of our study was originally the further development of our recently discovered polo-like kinase 1 (PLK1) inhibitors. A series of new 2,4-disubstituted pyrimidine derivatives were synthesized around the original hit, but their PLK1 inhibitory activity was very poor. However the novel compounds showed nanomolar CDK9 inhibitory activity and very good antiproliferative effect on multiple myeloma cell lines (RPMI-8226).