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首页> 外文期刊>American Journal of Physiology >Inactivation of amino acid receptors in medullary reticular formation modulates and suppresses ingestion and rejection responses in the awake rat.
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Inactivation of amino acid receptors in medullary reticular formation modulates and suppresses ingestion and rejection responses in the awake rat.

机译:髓质网状结构中氨基酸受体的失活可调节和抑制清醒大鼠的摄取和排斥反应。

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摘要

The lateral medullary reticular formation (RF) is the source of many preoromotor neurons and is essential for generation of ingestive consummatory responses. Although the neurochemistry mediating these responses is poorly understood, studies of fictive mastication suggest that both excitatory and inhibitory amino acid receptors play important roles in the generation of these ororhythmic behaviors. We tested the hypothesis that amino acid receptors modulate the expression of ingestion and rejection responses elicited by natural stimuli in awake rats. Licking responses were elicited by either intraoral (IO) gustatory stimuli or sucrose presented in a bottle. Oral rejection responses (gaping) were elicited by IO delivery of quinine hydrochloride. Bilateral microinjection of the N-methyl-D-aspartate (NMDA) receptor antagonist d-[(3)-2-carboxypiperazin-4-yl]-propyl-1-phosphonic acid (D-CPP) suppressed licking and gape responses recorded electromyographically from a subset of orolingual muscles. Likewise, infusion of the non-NMDA receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) significantly reduced licking and gape responses but was accompanied by spontaneous gasping responses. Rats still actively probed the bottle, indicating an intact appetitive response. Neither D-CPP nor CNQX differentially affected ingestion or rejection, suggesting that the switch from one behavior to the other does not simply rely on one glutamate receptor subtype. Nevertheless, a glutamate receptor-mediated switch from consummatory behavior to gasps after CNQX infusions suggests a multifunctional substrate for coordinating the jaw and tongue in different behaviors. Bilateral infusions of the GABA(A) receptor antagonist bicuculline or the glycine receptor antagonist strychnine enhanced the amplitude of IO stimulation-induced oral responses. These data suggest that the neural substrate underlying ingestive consummatory responses is under tonic inhibition. Release of this inhibition may be one mechanism by which aversive oral stimuli produce large-amplitude mouth openings associated with the rejection response.
机译:外侧髓样网状结构(RF)是许多原运动神经元的来源,对于产生消化吸收反应至关重要。尽管人们对调解这些反应的神经化学知之甚少,但有关虚构咀嚼的研究表明,兴奋性氨基酸受体和抑制性氨基酸受体在产生这些矫正性行为方面均起着重要作用。我们测试了以下假设:氨基酸受体调节清醒大鼠中自然刺激引起的摄取和排斥反应的表达。口内(IO)味觉刺激或瓶子中的蔗糖引起舔食反应。口服奎宁盐酸盐引起口服排斥反应(呕吐)。 N-甲基-D-天冬氨酸(NMDA)受体拮抗剂d-[(3)-2-羧基哌嗪-4-基]-丙基-1-膦酸(D-CPP)的双边显微注射抑制了肌电记录的舔and和气隙反应来自口头肌肉的子集。同样,输注非NMDA受体拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)可显着减少舔ing和气孔反应,但伴有自发喘气反应。大鼠仍在积极探测该瓶子,表明其完整的食欲反应。 D-CPP和CNQX都不会对摄入或排斥产生不同的影响,这表明从一种行为向另一种行为的转换并不仅仅依赖于一种谷氨酸受体亚型。然而,在CNQX输注后,谷氨酸受体介导的从消耗行为向喘息转变表明,多功能底物可协调下颌和舌头的不同行为。 GABA(A)受体拮抗剂双瓜氨酸或甘氨酸受体拮抗剂士的宁的双侧输注增加了IO刺激引起的口服反应的幅度。这些数据表明,消化吸收反应背后的神经基质处于强直抑制下。释放这种抑制作用可能是一种厌恶性口腔刺激产生与排斥反应相关的大幅度张口的机制。

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