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  • Spinal cord  (2)
  • $$\dot V_{\max }$$ membrane potential relationship  (1)
  • A-type natriuretic peptide  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    FEBS Letters 276 (1990), S. 209-213 
    ISSN: 0014-5793
    Keywords: A-type natriuretic peptide ; B-type natriuretic peptide ; C-type natriuretic peptide ; Neuropeptide ; Precursor structure ; cDNA cloning
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 309 (1979), S. 179-190 
    ISSN: 1432-1912
    Keywords: Antiarrhythmic drug ; Procainamide ; Cardiac transmembrane action potential ; $$\dot V_{\max }$$ membrane potential relationship ; Reactivation of $$\dot V_{\max }$$
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Effects of procainamide (PA), 0.18, 0.37 and 0.74 mmol/l, on the transmembrane potential were studied in isolated guinea-pig papillary muscles, superfused with modified Tyrode's solution (external K concentration, [K]o=5.4 mmol/l) at the basic driving rate of 1 Hz. PA, at 0.37 mmol/l, significantly reduced the maximum rate of rise of action potential ( $$\dot V_{\max }$$ ) with no change in the resting potential. When 2.7 mmol/l [K]o of the superfusate was exchanged for 15 mmol/l [K]o solution a decrease in $$\dot V_{\max }$$ induced by 0.37 mmol/l PA became more prominent with decrease in resting potential. The reduction of $$\dot V_{\max }$$ at steady state was less at lower driving rates (0.25 and 0.5 Hz) and more at higher driving rates (2–5 Hz) than at 1 Hz in 2.7, 5.4 and 10.0 mmol/l [K]o solution. Such changes were enhanced concentration-dependently by PA at 5.4 mmol/l [K]o. Also, the changes became more significant with an increase in [K]o from 2.7 mmol/l to 5.4 mmol/l and then to 10.0 mmol/l. The recovery process of $$\dot V_{\max }$$ proceeded with two components. The time course of the slow component seen in the $$\dot V_{\max }$$ of the first response after interruption of basic driving stimulation at 1 Hz, followed an approximate monoexponential function. The time constants were 6.3, 4.4 and 5.8 s in the presence of 0.18, 0.37 and 0.74 mmol/l PA at 5.4 mmol/l [K]o and 3.4 and 3.7 s both in the presence of 0.37 mmol/l PA at 2.7 and 10.0 mmol/l [K]o. $$\dot V_{\max }$$ values after 30 or 60 s interruption of stimulation were 80–92% of the predrug $$\dot V_{\max }$$ value at 1 Hz. The time constants of the first component, estimated by the peeling-off methods at the driving rate of 0.1 Hz, were 11, 31 and 5–22 ms in the presence of 0.37 mmol/l at 5.4, 10.0 and 2.7 mmol/l [K]o and did not differ significantly from the time constants in control preparations. The results were found to be consistent, to a certain extent, with the model proposed by Hondeghem and Katzung (1977).
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-0878
    Keywords: Serotonin fibers ; Spinal cord ; Immunohistochemistry ; Monkey (Macaca fuscata)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A modified procedure of PAP-immunohistochemistry with the use of a rabbit antiserum against serotonin was applied to investigate the pattern of serotonin-containing nerve fibers in the spinal cord of the monkey, Macaca fuscata. The majority of descending serotonin fibers in the white matter is located immediately below the pia mater in the ventrolateral funiculi. Lamina I and the outer zone of lamina II are supplied with numerous serotonin fibers. In the intermediate gray, two prominent bundles composed of longitudinal fibers, i.e., lateral and medial longitudinal serotonin bundles, were recognized at the lateral column and in the vicinity of the central canal, respectively. The motoneurons of the anterior horn are encompassed by fine networks of serotonin fibers and terminals. The results obtained from studies with the monkey spinal cord closely resemble those characteristic of the dog spinal cord as presented in a previous paper, except for portions of the lumbar level. In segments L3–L4, intercalated cell groups between the medial and lateral motor nuclei receive particularly rich inputs of serotonin fibers in the same manner as the neurons of the nucleus intermediolateralis. This peculiar finding may suggest the presence of a specialized nucleus in the anterior column of the simian and also human spinal cord.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 226 (1982), S. 477-491 
    ISSN: 1432-0878
    Keywords: Serotonin fibers ; Spinal cord ; Immunohistochemistry ; Dog
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Distribution of serotonin fibers in the spinal cord of the dog was investigated by means of a modified PAP method; a rabbit anti-serotonin serum prepared in the laboratory of the authors was used in this study. Serotonin fibers were revealed as PAP-positive dark-brown elements displaying dot-like varicosities (0.5–2.0 μm in diameter). In the spinal cord of the dog, the distribution of serotonin fibers is extensive. These fibers occur more densely in more caudal segments and are most prominent at the sacrococcygeal level. From the level of the cervical spinal cord to the upper lumbar region, the descending serotonin fibers are located immediately under the pia mater in the ventrolateral portion of the lateral funiculus. In more caudal segments, serotonin fibers are dispersed throughout the ventral and lateral funiculi. These longitudinal en passage-fibers send numerous transverse collaterals to the gray matter. Serotonin fibers are distributed abundantly in the laminae I and III of the posterior column, while only a few fibers are found in the lamina II (substantia gelatinosa). In the intermediate zone, two descending serotonin pathways, i.e., lateral and medial longitudinal bundles, are observed to coincide topographically with the nucleus intermediolateralis at C8(T1)-L3(L4) and the nucleus intermediomedialis at C1-Co respectively. The former is particularly prominent and communicates with the contralateral bundle via commissural bundles at intervals of 300–500 μm. The large motoneurons in the anterior column, especially those in the nucleus myorabdoticus lateralis within the cervical and lumbar enlargements, are closely surrounded by fine networks of serotonin fibers and terminals.
    Type of Medium: Electronic Resource
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