BUSchges A
J Exp Biol. 1994 Apr;189(1):285-92. doi: 10.1242/jeb.189.1.285.
The leg joints of invertebrates are governed by neural control loops that control their position and velocity during movements (for reviews, see Bassler, 1983, 1993). These neural control loops rely on sensory feedback about the position and velocity of the controlled leg joint. In invertebrates, this sensory feedback is provided by external (e.g. hair fields, hair rows) and/or internal sense organs (e.g. chordotonal organs). The femoral chordotonal organ (fCO) serves as the main proprioceptor in the control loop governing the femur-tibia (FT) joint of the insect leg. The fCO measures the position and movement of this joint (e.g. Bassler, 1965, 1993; Burns, 1974; Usherwood et al. 1968; Zill, 1985). Previous investigations have described the physiology of sensory cells within femoral chordotonal organs (e.g. stick insect, Hofmann et al. 1985; Hofmann and Koch, 1985; locust, Matheson, 1990; Matheson and Field, 1990). Numerous investigations have been undertaken into the central processing of sensory information provided by the fCO to gain an insight into the control of FT joint movement during different behavioural tasks, for example during resistance reflexes in the standing animal (locust, Burrows, 1987, 1988; Burrows et al. 1988; stick insect, Bassler, 1988; Buschges, 1989, 1990; Driesang and Buschges, 1993) or during active movements (stick insect, Bassler, 1988; Bassler and Buschges, 1990). Most previous studies have not, however, taken into account the morphological separation of the fCO into two distinct scoloparia in the legs of some species (stick insect, Fuller and Ernst, 1973; Hofmann et al. 1985; Hofmann and Koch, 1985; locust middle leg, Burns, 1974). It has been inferred that the whole fCO supplies position and velocity information about the FT joint. In contrast, recent studies of leg reflexes have shown that only its smaller scoloparium (Fig. 1A), containing approximately one-sixth of the total number of sensory neurones, provides the sensory information that is used by the FT control loop (locust, Field and Pfluger, 1989; stick insect, Kittmann and Schmitz, 1992). These studies did not show what types of sensory neurones are located in the ventral part of the fCO and thus contribute to the FT control loop. We have therefore investigated the physiology of sensory neurones that are located in the ventral scoloparium of the fCO.
无脊椎动物的腿部关节受神经控制回路支配,这些回路在运动过程中控制关节的位置和速度(综述见Bassler,1983年、1993年)。这些神经控制回路依赖于有关被控制腿部关节位置和速度的感觉反馈。在无脊椎动物中,这种感觉反馈由外部(如毛场、毛排)和/或内部感觉器官(如弦音器官)提供。股弦音器官(fCO)是昆虫腿部控制股胫(FT)关节的控制回路中的主要本体感受器。fCO测量该关节的位置和运动(如Bassler,1965年、1993年;Burns,1974年;Usherwood等人,1968年;Zill,1985年)。先前的研究描述了股弦音器官内感觉细胞的生理学(如竹节虫,Hofmann等人,1985年;Hofmann和Koch,1985年;蝗虫,Matheson,1990年;Matheson和Field,1990年)。已经对fCO提供的感觉信息的中枢处理进行了大量研究,以深入了解在不同行为任务期间FT关节运动的控制,例如在站立动物的抵抗反射期间(蝗虫,Burrows,1987年、1988年;Burrows等人,1988年;竹节虫,Bassler,1988年;Buschges,1989年、1990年;Driesang和Buschges,1993年)或在主动运动期间(竹节虫,Bassler,1988年;Bassler和Buschges,1990年)。然而,大多数先前的研究没有考虑到在某些物种(竹节虫,Fuller和Ernst,1973年;Hofmann等人,1985年;Hofmann和Koch,1985年;蝗虫中腿,Burns,1974年)的腿部fCO在形态上分为两个不同的 scoloparia 。据推测,整个fCO提供有关FT关节的位置和速度信息。相比之下,最近对腿部反射的研究表明,只有其较小的scoloparium(图1A),包含约六分之一的感觉神经元总数,提供FT控制回路使用的感觉信息(蝗虫,Field和Pfluger,1989年;竹节虫,Kittmann和Schmitz,1992年)。这些研究没有表明位于fCO腹侧部分的感觉神经元类型,因此也没有表明哪些感觉神经元对FT控制回路有贡献。因此,我们研究了位于fCO腹侧scoloparium的感觉神经元的生理学。