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Grey columns

The grey columns are three regions of the somewhat ridge-shaped mass of grey matter in the spinal cord. These regions present as three columns: the anterior grey column, the posterior grey column, and the lateral grey column, all of which are visible in cross-section of the spinal cord.

Structure
Anterior grey column s in the anterior grey column of the spinal cord The anterior grey column, (also known as the anterior horn of spinal cord and anterior cornu) is broad and of a rounded or quadrangular shape. Its posterior part is termed the base, and its anterior part the head, but these are not differentiated from each other by any well-defined constriction. It is separated from the surface of the spinal cord by a layer of white substance which is traversed by the bundles of the anterior nerve roots. In the thoracic region, the posterolateral part of the anterior column projects laterally as a triangular field, which is named the lateral grey column. It comprises three different types of neurons, two types of lower motor neuron – large alpha motor neurons, and medium gamma motor neurons, and small neurons thought to be interneurons. They are organized in the same manner as the muscles they innervate. Gamma motor neurons Gamma motor neurons innervate intrafusal muscle fibers that control the sensitivity of muscle spindles to stretch. They have smaller cell bodies than alpha motor neurons and do not receive proprioceptive input. Posterior grey column The posterior grey column, also known as the posterior (or dorsal) horn of spinal cord, is subdivided into six layers known as Rexed laminae, based on the type of sensory information sent to each section. • Marginal nucleus of spinal cord (lamina I) • Substantia gelatinosa of Rolando (lamina II) • Nucleus proprius (laminae III, IV) • Spinal lamina V, the neck of the posterior horn • Spinal lamina VI, the base of the posterior horn. The other four laminae are located in the other two grey columns in the spinal cord. The function of the spinal dorsal horn is to process and integrate sensory information from the peripheral nervous system. It receives inputs from primary afferent fibers and modulatory systems, and it projects to higher brain centers and motor neurons. The dorsal horn circuitry is involved in various aspects of sensory processing, including discrimination, integration, and modulation of nociceptive and non-nociceptive signals. Dysfunction of the dorsal horn circuitry has been implicated in chronic pain conditions and other neurological disorders. Laminae I and II receive information from afferent neurons that sense nociception, temperature, and itching, laminae III and IV are sent information from neurons that sense mechanical pressure, and laminae V and VI are sent information from proprioceptors. It is known to be the primary relay point for haptic and nociceptive messages. The function of the spinal dorsal horn is to process and integrate sensory information from the peripheral nervous system. It receives inputs from primary afferent fibers and modulatory systems, and it projects to higher brain centers and motor neurons. The dorsal horn circuitry is involved in various aspects of sensory processing, including discrimination, integration, and modulation of nociceptive and non-nociceptive signals. Dysfunction of the dorsal horn circuitry has been implicated in chronic pain conditions and other neurological disorders. Lamina I Lamina I is also known as the marginal nucleus of spinal cord. The majority of posterior column projection neurons are located in lamina I, however most neurons in this layer are interneurons. The main areas these neurons innervate are the caudal ventrolateral medulla (CVLM), the nucleus of the solitary tract (NTS), the lateral parabrachial area (LPb), the periaqueductal grey matter (PAG), and certain regions in the thalamus. The CVLM receives nociceptive and cardiovascular responses. The NTS receives cardio-respiratory inputs and affects reflex tachycardia from noxious stimulation. The LPb projects to the amygdala and hypothalamus and is involved in the emotional response to pain. The PAG develops ways to deal with pain and is a main target of analgesics. It projects to other parts of the brainstem. The nuclei of the thalamus affect sensory and motivational aspects of pain. The neurons of this lamina can be distinguished by their morphology as pyramidal, spindle, or multipolar. Lamina II This layer is also known as the substantia gelatinosa of Rolando and has the highest density of neurons. These neurons mediate the activity of nociceptive and temperature afferent fibers. Laminae III and IV These laminae are also known as the nucleus proprius and contain a much smaller density of neurons than lamina II. Lamina V This lamina is also known as the neck of the posterior column and receives information from mechanoreceptors and danger information from nociceptors. Lateral grey column The lateral grey column, or the lateral horn of spinal cord, is part of the sympathetic nervous system and receives input from brain stem, organs, and hypothalamus. The lateral column is only present in the thoracic region and upper lumbar segments. The lateral grey column contains preganglionic cell bodies of the autonomic nervous system and sensory relay neurons. ==Clinical significance==
Clinical significance
Neurons in the anterior column have been shown to be affected by amyotrophic lateral sclerosis (ALS). The number of large alpha motor neurons and medium gamma motor neurons was greatly reduced and the number of small neurons was either slightly or greatly reduced depending on the type of ALS. Muscular atrophy has also been shown to have an effect on neurons of the anterior column. A large loss of large alpha motor neurons, medium gamma motor neurons, and small neurons was recorded in cases of muscular atrophy. Damage to the lateral column can result in Horner's syndrome. Multiple system atrophy (MSA), has also been linked to the lateral grey column. MSA has been shown to reduce the cell count in the lateral column by over 50%. The posterior column has a prominent role in the pain system, it is the first central relay in the nociceptive pathway. The first-order afferent neuron carries sensory information to the second order neuron in the dorsal horn. The axon of the second order neuron, if it is a projection neuron and not an interneuron, then goes to the third order neuron in the thalamus. The thalamus is known as the "gateway to the cortex". The third order neuron then goes to the cerebral cortex. The afferent neurons are either A fibers or C fibers. A fibers are myelinated allowing for faster signal conduction. Among these there are A beta fibers which are faster and carry information about non-painful touch and A delta fibers which are slower and thinner than the A beta fibers. The C fibers are not myelinated and therefore slower. The two types terminate in very different areas. Non-peptidergic C fibers are linked to the skin, where they innervate the epidermis while peptidergic C fibers innervate other tissues and deeper parts of the skin. Affective Affective nociceptive signals affect emotions. These signals go to the limbic system and tell the body to react to the danger stimulus (i.e. removing a hand from a hot stove). These neurons have larger receptive fields because the emotional reaction to most pain stimuli is similar. ==See also==
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