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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Guileless

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

過剩

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

Obscure

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

MANIA

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

BAIT

抑制

originality

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

Cumbersome

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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