Neurotransmitters and receptors in the dorsal horn of the spinal cord
نویسنده
چکیده
Modulation of the sensory input can occur within the dorsal horn of the spinal cord where the primary afferent fibers synapse with neurons that transmit to the higher centers. The transmission of the sensory information begins with activation of the peripheral receptors of primary afferent neurons whose cell bodies lie within the dorsal root ganglia and whose central terminals project to secondary neurons in the dorsal horn of the spinal cord. Several neurotransmitters and a large variety of receptors have been found in the superficial laminae of the dorsal horn. The present work reviews the major classes of transmitters and receptors that have been implicated in the transmission and modulation of spinal afferent and pain processing. The role of excitatory and inhibitory amino acids, tachykinin and opioid peptides, calcitonin gene-related peptide (CGRP), nociceptin and nocistatin, biogenic amines, acetylcholine, ATP, nitric oxide as well as capsaicin and vanilloid receptors will be discussed along with the most recent developments in the field. It seems probable that transmission of the somatosensory information from the primary afferent fibers to the secondary dorsal horn neurons depends on the balance between the excitatory effects of excitatory amino acids and the inhibitory actions of several other transmitter systems. Acta Biol Szeged 44(1-4):21-38 (2000)
منابع مشابه
Propofol differentially inhibits the release of glutamate, γ-aminobutyric acid and glycine in the spinal dorsal horn of rats
Objective(s): Propofol (2, 6-diisopropylphenol) is an intravenous anesthetic that is commonly used for the general anesthesia. It is well known that the spinal cord is one of the working targets of general anesthesia including propofol. However, there is a lack of investigation of the effects of propofol on spinal dorsal horn which is important for the sensory transmission of nociceptive signal...
متن کاملRole of Presynaptic Glutamate Receptors in Pain Transmission at the Spinal Cord Level
Nociceptive primary afferents release glutamate, activating postsynaptic glutamate receptors on spinal cord dorsal horn neurons. Glutamate receptors, both ionotropic and metabotropic, are also expressed on presynaptic terminals, where they regulate neurotransmitter release. During the last two decades, a wide number of studies have characterized the properties of presynaptic glutamatergic recep...
متن کاملRole of nitric oxide and Jun N-terminal kinase in the development of dark neurons in the dorsal horn of the spinal cord following induction of inflammatory pain
Introduction: Dark neurons which their morphological characteristics are consistent with those of cells undergoing apoptosis, are generated as an acute or delayed consequence of several pathological situations. The present study was designed to evaluate whether inflammatory pain regarding the role of NO and JNK lead to the formation of dark neurons in the dorsal horn of the lumbar spinal cor...
متن کاملXenon inhibits excitatory but not inhibitory transmission in rat spinal cord dorsal horn neurons
BACKGROUND The molecular targets for the promising gaseous anaesthetic xenon are still under investigation. Most studies identify N-methyl-D-aspartate (NMDA) receptors as the primary molecular target for xenon, but the role of alpha-amino-3-hydroxy-5-methyl-4-isoxazole-4-propionic acid (AMPA) receptors is less clear. In this study we evaluated the effect of xenon on excitatory and inhibitory sy...
متن کاملRole of kainate receptors in nociception.
Nociceptive nerve fibers use L-glutamate as a fast excitatory neurotransmitter and it is therefore not surprising that both, ionotropic and metabotropic glutamate receptors play pivotal roles for transmission of nociceptive information in spinal cord. A subtype of ionotropic glutamate receptors, the kainate receptor, is present in spinal dorsal horn. However, its role has remained obscure as sp...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2000