Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:1.11.1.7 (peroxidase)
 65,474 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Electrophysiological and horseradish peroxidase (HRP) techniques have provided new insights into the organization of the sacral parasympathetic reflex pathways to the large intestine and urinary bladder. The innervation of the two organs arises from separate groups of sacral preganglionic cells: (1) a dorsal band of cells in laminae V and VI providing an input to the intestine; and (2) a lateral band of cells in lamina VII providing an input to the bladder. These two groups of cells were separated by an interband region containing tract cells and interneurons. Neurons in the interband region received a visceral afferent input and exhibited firing correlated with the activity of intestine and urinary bladder. It seems reasonable therefore to consider the interband region as a third component of the sacral parasympathetic nucleus. Anterograde transport of HRP revealed that visceral afferents from the intestine and bladder projected into the parasympathetic nucleus. Most of the projections were collaterals from afferent axons in Lissauer's tract that passed in lamina I laterally and medially around the dorsal horn. These afferent collaterals were located in close proximity to preganglionic perikarya and dendrites in laminae I, V and VI. The proximity of visceral afferents and efferents in the sacral cord probably reflects the existence of polysynaptic rather than monosynaptic connections since electrophysiological studies revealed that both the defecation and micturition reflexes occurred with very long central delays (45-70 msec). The reflex pathways mediating defecation and micturition in cats with an intact neuraxis were markedly different. Defecation was dependent upon a spinal reflex with unmyelinated (C-fiber) peripheral afferent and efferent limbs. On the other hand, micturition was mediated by a spinobulbospinal pathway with myelinated peripheral afferent (A-fiber) and efferent axons (B-fiber). Transection of the spinal cord at T12-L2 blocked the micturition reflex but only transiently depressed the defecation reflex. In chronic spinal cats the micturition reflex recovered 1-2 weeks after spinalization; however, in these animals bladder-to-bladder micturition reflexes were elicited by C-fiber rather than A-fiber afferents. The C-fiber afferent-evoked reflex was weak or undetectable in animals with an intact neuraxis. Transection of the spinal cord also changed the micturition reflex in neonatal kittens (age 5-28 days). In neonates with an intact neuraxis bladder-to-bladder reflexes occurred via a long latency spinobulbospinal pathway (325-430 msec). The long latency is attributable to the slow conduction velocity in immature unmyelinated peripheral and central axons. In chronic spinal kittens (3-7 days after spinalization) the long latency reflex was abolished and a shorter latency (90-150 msec) bladder reflex was unmasked. The emergence of this spinal pathway may reflect axonal sprouting and the formation of new reflex connections within the sacral parasympathetic nucleus.
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PMID:Organization of the sacral parasympathetic reflex pathways to the urinary bladder and large intestine. 626 84

Using Golgi preparations from adult cat and monkey the present study describes the general arborization pattern of primary afferent collaterals to the marginal layer (lamina I) of the dorsal horn. The dorsal root origin of the golgi-impregnated afferents was verified in the cat by matching the structural properties of these fibers with horseradish peroxidase (HRP)-stained primary afferents which were filled with HRP via anterograde transport through dorsal rootlets. The marginal afferents, in both the cat and the monkey, are relatively fine-caliber fibers which emanate from the dorsolateral fasciculus of Lissauer. Superficially they form a transverse plexus of fibers which runs across the surface of the dorsal horn and is especially dense in the lateral portion of the dorsal aspect of the marginal layer where lamina I is thickest. In deeper regions of the marginal layer, marginal afferents are longitudinally oriented and have collaterals within the outer zone of lamina II. In both superficial and deep regions of the marginal layer the afferents run parallel with large numbers of marginal cell dendrites. Most marginal afferents give rise to collaterals with widely spaced, round to oval "boutons en passant" and "boutons terminaux" which are 1.5-2.0 micrometers in diameter. Structural correlation with previous physiological and anatomical studies suggest that most of these fibers are finely myelinated, A-delta, high-threshold mechanoreceptive fibers.
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PMID:Primary afferent distribution pattern in the marginal zone (lamina 1) of adult monkey and cat lumbosacral spinal cord. 627 51

Retrograde and transganglionic transport of horseradish peroxidase (HRP) was used to trace afferent and efferent pathways in the left inferior cardiac nerve of the cat. Cardiac efferent and afferent neurons were located, respectively, in the stellate ganglion (average cell count per experiment:2679) and in the ipsilateral dorsal root ganglia (DRG) from C8 to T9 (average cell count per experiment:213). Labeled cardiac afferent projections to the spinal cord were most dense in segments T2-T6 where they were located in Lissauer's tract and in lamina 1 on the lateral border of the dorsal horn. Labeled afferent axons extended ventrally through lamina 1 into lamina 5 and the dorsolateral region of lamina 7 in proximity to the intermediolateral nucleus. A weak projection was noted on the medial side of the dorsal horn. These sites of termination are similar to projections by other sympathetic afferent pathways (i.e. renal, hypogastric and splanchnic nerves) to the lower thoracic and lumbar spinal cord, indicating that visceral afferents may have a uniform pattern of termination at various segmental levels. This pattern of termination in regions of the gray matter containing spinothalamic tract neurons and neurons involved in autonomic mechanisms is consistent with the known functions of sympathetic afferent pathways in nociception and in the initiation of autonomic reflexes.
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PMID:Tracing of afferent and efferent pathways in the left inferior cardiac nerve of the cat using retrograde and transganglionic transport of horseradish peroxidase. 649 6

Cranial nerves IX and X in frogs have been described as originating from a nuclear group referred to as the IX-X complex. We studied the central nervous system components of this complex in Rana pipiens and R. catesbiana by labeling peripheral branches of cranial nerves IX and X and identifying the central nervous system contributions of these branches. Various peripheral nerves (IX and the cardiac, gastric, pulmonary, and laryngeal branches of X) were identified and soaked in horseradish peroxidase (HRP). One to 2 weeks later, the frogs were killed and processed for HRP by the tetramethylbenzidine method. Glossopharyngeal efferents originated from a small ventrolateral cell group found at the level of IX root exit. Vagal efferents formed a single column of cells in a ventrolateral position from the level of the brainstem exist of the vagus nerve (approximately 2,000 micrometers above the obex) to 200 micrometers below the obex (values given are for an 80-g frog). This cell group was separate from and just caudal to efferent cells of the glossopharyngeal nerve. Within the vagal portion of the column, cells projecting through the gastric branch were found throughout the rostral-caudal extent of the nucleus. "Cardiac" cells tended to be more rostral than "pulmonary" cells, and both groups of cells were located in the middle of the nucleus. "Laryngeal" cells were located more caudally in the nucleus. This peripheral representation within the vagal nucleus corresponds more closely to the organization found in the mammalian nucleus ambiguus, rather than to the apparent lack of organization found in the mammalian dorsal motor nucleus. Afferents of IX and X entered slightly rostral to the ventral roots of their respective nerves and descended in two tracts. The majority entered the tractus solitarius and descended in a medial position to cervical spinal cord. A portion of the afferents from the vagus nerve crossed the midline in the lower myelencephalon just dorsal to the central canal and ascended a short distance on the contralateral side. Within the solitary tract, vagal afferents were located in a ventrolateral position as they descended to below the obex. Glossopharyngeal afferents filled the remainder of the tract. A smaller portion of afferents from both IX and X did not enter the solitary tract but descended in the spinal tract of V and the dorsolateral funiculus of the spinal cord (Lissauer's tract) to thoracic levels. Afferents of IX also formed a rostral bundle which extended in the solitary tract to the caudal metencephalon.
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PMID:Organization within the cranial IX-X complex in ranid frogs: a horseradish peroxidase transport study. 660 37

The relationship of lumbar dorsal root afferents to lateral motor column motoneurons was studied using anterograde injury filling of dorsal roots and retrograde injury filling of ventral roots with horseradish peroxidase. At the light microscopic level, horseradish peroxidase labelled dorsal root axons were observed to separate into a medial division of large diameter axons which enter the dorsal funiculus and a lateral division of small diameter axons which form a compact bundle in the dorsolateral funiculus which may be homologous to the mammalian tract of Lissauer. Within the spinal gray, primary afferents terminate in two distinct regions. The more ventral of these terminal fields, which receives collaterals of primary afferent axons in the dorsal funiculus, overlaps the dendritic arborizations of the lateral motor column motoneurons. Some axons leave the ventral terminal field to enter the dorsal lateral motor column. Here they terminate on the primary dendrites and somata of lateral motor column motoneurons. At the electron microscopic level, labelled primary afferent terminals were seen to synapse upon lateral motor column motoneuron dendrites as well as upon the somata of dorsally positioned lateral motor column motoneurons. These terminals contain small spherical vesicles and occasional dense-cored vesicles. The synaptic specializations are characterized by a small amount of postsynaptic material. The lateral motor column may be divided into dorsal and ventral portions on the basis of the primary afferent distribution and this is in accord with functional, physiological and developmental data.
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PMID:The relationship of dorsal root afferents to motoneuron somata and dendrites in the adult bullfrog: a light and electron microscopic study using horseradish peroxidase. 661 Aug 40

The central projection fields of cutaneous neurons of the rat's major occipital nerve have been investigated using the method of transganglionic transport of horseradish peroxidase (HRP), with tetramethylbenzidine according to Mesulam (1978) as the chromogen. Furthermore, the course of the nerve, diameter distribution of myelinated axons, and diameter distribution of HRP-labeled perikarya of spinal ganglion cells belonging to this nerve, diameter distribution of myelinated axons, and diameter distribution of HRP-labeled perikarya of spinal ganglion cells belonging to this nerve have been studied. Following HRP application to the proximal stump of the cut nerve, labeled structures were found ipsilaterally in the cervical spinal cord and in the medulla oblongata. In the spinal cord, reaction product was mainly concentrated in the lateral parts of laminae I-III of the dorsal horn in segments C2 and C3. In C1, primary afferent terminals were more sparsely distributed and restricted to laminae I and II. Reaction product was also seen in the tract of Lissauer in segments C1-C4. In the medulla oblongata HRP labeled structures were observed in the medial cuneate nucleus, in the rostral part of the external cuneate nucleus, and in the nucleus of the spinal tract of the trigeminal nerve. A possible somatotopic arrangement of central terminals of cutaneous neurons within the cervical dorsal horn, as well as differences between the projection fields of muscle and skin afferents within the upper cervical cord and caudal medulla are discussed.
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PMID:Afferent projections of the rat major occipital nerve studied by transganglionic transport of HRP. 662 96

Immunohistochemical studies revealed that vasoactive intestinal polypeptide (VIP) is localized primarily to sacral segments of the cat's spinal cord. VIP is most prominent in afferent axons and terminals in Lissauer's tract and in lateral laminae I and V of the dorsal horn. The distribution of VIP terminals is very similar to that of visceral afferent projections identified by horseradish peroxidase. Dye-tracing experiments combined with immunohistochemistry demonstrated that VIP is located in visceral afferent perikarya in the sacral dorsal root ganglia and also in terminals in the sacral autonomic nucleus. These observations suggest that VIP is a neurotransmitter in afferent projections from the pelvic viscera.
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PMID:Vasoactive intestinal polypeptide in visceral afferent pathways to the sacral spinal cord of the cat. 666 34

The projections of afferent renal fibers (ARN) to dorsal root ganglia and into the spinal cord of the rat were studied using the anterograde transport of horseradish peroxidase (HRP). Crystalline HRP was applied to the proximal cut ends of renal nerves or injected as a concentrated solution into the kidney, on either the right or left side. After a survival time of 40-120 h, sections of thoraco-lumbar dorsal root ganglia (DRG) and spinal cord were cut and processed according to the tetramethyl benzidine method. HRP applied either to the ARN or to the kidney on the left labeled neurons in the DRG from T8 to L2. On the other hand, HRP application on the right side resulted in labeling of neurons in DRG T6 to T13. No labeled neurons were found in the contralateral DRG. Labeled neurons in the DRG were of the small (11-20 micron) and medium (30-42 micron) size and were distributed in all portions of the DRG. In the spinal cord the greatest concentration of labeled ARN from the left were found in segments T10-L1, whereas projections from the right ARN were concentrated primarily in segments T7-T10. Labeled fibers entered along the medial aspect of the ipsilateral dorsal horn and projected both rostrally and caudally in the medial portion of Lissauer's tract, sending some collaterals into lamina I. The majority of labeled fibers coursed ventrally along the medial aspect of the dorsal horn towards the midline where they terminated in the region of the dorsal gray commissure, just dorsal to the central canal. Additionally, labeled fibers from the medial projection passed into laminae III-V. No labeled fibers or terminals were observed in the contralateral spinal cord. These data show that ARN enter the spinal cord through several DRG and provide the first anatomical demonstration of central sites of termination of ARN. These spinal sites of projection of sensory information from the kidney are likely to be central sites of integration of reno-renal and visceral reflexes.
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PMID:Central projections of afferent renal fibers in the rat: an anterograde transport study of horseradish peroxidase. 666 88

The segmental and central distributions of renal nerve afferents in adults cats and kittens were studied by using retrograde and transganglionic transport of horseradish peroxidase (HRP). Transport of HRP from the central cut ends of the left renal nerves labelled afferent axons in the ipsilateral minor splanchnic nerves and sensory perikarya in the dorsal root ganglia from T12 to L4. The majority of labeled cells (85%) were located between L1 and L3. A few neurons in the contralateral dorsal root ganglia were also labeled. Labeled cells were not confined to any particular region within a dorsal root ganglion. Some examples of bifurcation of the peripheral and central processes within the ganglion were noted. A small number of preganglionic neurons, concentrated in the intermediolateral nucleus, were also identified in some experiments. In addition, many sympathetic postganglionic neurons were labeled in the renal nerve ganglia, the superior mesenteric ganglion, and the ipsilateral paravertebral ganglia from T12 to L3. Transganglionic transport of HRP labeled renal afferent projections to the spinal cord of kittens from T11 to L6, with the greatest concentrations between L1 and L3. These afferents extended rostrocaudally in Lissauer's tract and sent collaterals into lamina I. In the transverse plane, a major lateral projection and a minor medial projection were observed along the outer and inner margins of the dorsal horn, respectively. From the lateral projection many fibers extended medially in laminae V and VI forming dorsal and ventral bundles around Clarke's nucleus. The dorsal bundle was joined by collaterals from the medial afferent projection and crossed to the contralateral side. The ventral bundle extended into lamina VII along the lateroventral border of Clarke's nucleus. Some afferents in the lateral projection could be followed ventrally into the dorsolateral portion of lamina VII in the vicinity of the intermediolateral nucleus. In the contralateral spinal cord, labeled afferent fibers were mainly seen in laminae V and VI. These results provide the first anatomical evidence for sites of central termination of renal afferent axons. Renal inputs to regions (laminae I, V, and VI) containing spinoreticular and spinothalamic tract neurons may be important in the mediation of supraspinal cardiovascular reflexes as well as in the transmission of activity from nociceptors in the kidney. In addition, the identification of a bilateral renal afferent projection in close proximity to the thoracolumbar autonomic nuclei is consistent with the demonstration in physiological experiments of a spinal pathway for the renorenal sympathetic reflexes.
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PMID:Segmental distribution and central projections of renal afferent fibers in the cat studied by transganglionic transport of horseradish peroxidase. 686

Horseradish peroxidase was applied to the proximal stumps of severed cervical, thoracic and lumbar dorsal roots in the clawed toad, Xenopus laevis, in order to study the course, distribution and site of termination of dorsal root fibers in the spinal cord and brain stem. The anterograde transport of horseradish peroxidase as applied in the present study proved to be a useful and reliable technique. Results show that on entering the spinal cord, dorsal root fibers segregate into a medially placed component entering the dorsal funiculus and a more laterally situated bundle in the dorsal part of the lateral funiculus. As regards its position the latter bundle presumably represents the anuran homologue of the mammalian tract of Lissauer. Moreover, a small intermediate bundle of fibers directly enters the spinal gray matter. The labeled fibers entering the dorsal funiculus and the tract of Lissauer ascend and descend in the spinal cord, displaying a longitudinal arrangement resembling that of higher vertebrates. In the spinal gray, dorsal root fibers terminate in the dorsal, central and lateral fields of Ebbesson, with the last field being a major terminus for dorsal root fibers originating in the limb-innervating segments. No dorsal root fibers were found to project to the motoneuron fields. A dorsal column nucleus, which is divisible into medial and lateral compartments, is present in the obex region and extends from the level of the second spinal nerve to that of the entrance of the vagus and glossopharyngeal nerves. Dorsal root fibers from the lumbar and all thoracic segments project to the medial compartment of the dorsal column nucleus, whereas those of the cervical enlargement project to the lateral compartment. Although the anuran dorsal column nucleus appears to be less differentiated than that of higher vertebrates, its medial and lateral compartments can be considered to be the forerunners of the mammalian nucleus gracilis and nucleus cuneatus, respectively.
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PMID:Dorsal root projections in the clawed toad (Xenopus laevis) as demonstrated by anterograde labeling with horseradish peroxidase. 714 89


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