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Titlebook: Opioid Peptides and Blood Pressure Control; 11th Scientific Meet K. O. Stumpe,Karin Kraft,A. I. Faden Conference proceedings 1988 Springer-

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书目名称Opioid Peptides and Blood Pressure Control
副标题11th Scientific Meet
编辑K. O. Stumpe,Karin Kraft,A. I. Faden
视频video
图书封面Titlebook: Opioid Peptides and Blood Pressure Control; 11th Scientific Meet K. O. Stumpe,Karin Kraft,A. I. Faden Conference proceedings 1988 Springer-
出版日期Conference proceedings 1988
关键词Opioid; anatomy; blood vessel; cardiovascular; cardiovascular function; cardiovascular regulation; hyperte
版次1
doihttps://doi.org/10.1007/978-3-642-73429-8
isbn_softcover978-3-540-18935-0
isbn_ebook978-3-642-73429-8
copyrightSpringer-Verlag Berlin Heidelberg 1988
The information of publication is updating

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Distribution of Opioid Peptides Functionally Related to the Cardiovascular System9]. A crucial basis for the understanding of the complex mechanisms involved in this regulatory system is the detailed knowledge of the morphological distribution of opioid peptides. The morphological methods appropriate for this purpose require antisera raised against the different opioid peptides
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Studies on Enkephalinergic Mechanisms in Cardiovascular Centers of the Medulla Oblongata of the Rat responses and bradycardia upon intracisternal (i. c.) injection into the alpha-chloralose anesthetized rat [1]. Leu- and met-enkephalin and alpha neo-endorphin administered in the same way preferentially produced vasopressor actions, which with the two latter peptides were associated with bradycardi
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Multiplicity of Opioidergic Pathways Related to Cardiovascular Innervation: Differential Contributio (POMC), from which various opioid and nonopioid peptides can be processed, apparently in a tissue-specific manner (cf. Civelli et al. 1984; Goldstein 1984; Herz 1984; Udenfriend and Kilpatrick 1984; Civelli et al. 1985; Khachaturian et al. 1985; Kosterlitz 1985). Their distribution in areas of the
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Opioids, Opiate Receptors, and Central Cardiovascular Regulationmalian species [5]. It has long been known that exogenous opiates have potent cardiovascular actions after injections administered into the CNS; similarly, endogenous opioids are extremely active in producing cardiovascular changes after central administration [38]. In addition to the proposed role
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Role of Leu-morphin, an Opioid Peptide, in the Central Regulation of Fluid Balance and Blood Pressurituitary hormone (β-LPH) and adrenocorticotrophic hormone (ACTH) precursor (proopiomelanocortin), proenkephalin A, and proenkephalin B. Peptides derived from the same precursor coexist in the same cells, but the coexistence of two groups of opioid peptides in the same cell is not known. Therefore, t
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Endogenous Opioids in the Dorsal Vagal Complex and Resting Cardiovascular Function in the Anesthetiz in the rat selective mu-agonists increased mean arterial pressure (MAP) following injection into the nucleus of tractus solitarius (NTS) or dorsal motor nucleus of the vagus (DMV). However, heart rate (HR) was increased following injection into the NTS but unchanged following injection into the DMV
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