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Influence of CGRP (8-37), but not adrenomedullin (22-52), on the haemodynamic responses to lipopolysaccharide in conscious rats

机译:CGRP(8-37)而非肾上腺髓质素(22-52)对清醒大鼠对脂多糖的血流动力学反应的影响

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摘要

The functional involvement of the vasodilator peptides, adrenomedullin (ADM) and calcitonin gene-related peptide (CGRP), in the haemodynamic sequelae of continuous infusion of lipopolysaccharide (LPS) was assessed in conscious, male, Long Evans rats, by the use of peptide antagonists.It was demonstrated that ADM (22-52) at a dose of 500 nmol kg−1 h−1 caused significant inhibition of the effects of ADM (1 nmol kg−1), without affecting responses to CGRP (0.1 or 1 nmol kg−1).Even when the regional vasodilator responses to LPS infusion were enhanced (by pre-treatment with dexamethasone and the endothelin antagonist, SB 209670, or by pretreatment with SB 209670 and the AT1-receptor antagonist, losartan), ADM (22-52) had no significant cardiovascular effects. In contrast, the CGRP1-receptor antagonist, CGRP (8-37), caused small, but significant, inhibitions of the hypotensive and renal and mesenteric vasodilator effects of LPS, but only 6 h after onset of infusion in the presence of dexamethasone and SB 209670.The results indicate that, in this model of endotoxaemia, the marked regional vasodilatations seen in the presence of dexamethasone and SB 209670 do not involve ADM, but do involve CGRP, albeit only to a small extent.
机译:通过使用肽评估了在有意识的雄性Long Evans大鼠体内连续输注脂多糖(LPS)的血液动力学后遗症中血管扩张肽,肾上腺髓质素(ADM)和降钙素基因相关肽(CGRP)的功能。证明了ADM(22-52)的剂量为500 nmol kg-1 h-1时,可显着抑制ADM(1 nmol kg-1)的作用,而不会影响对CGRP的反应(0.1或1molnmol kg-1)即使对LPS输注的局部血管扩张药反应增强(通过地塞米松和内皮素拮抗剂SB 209670预处理,或SB 209670和AT1-受体拮抗剂洛沙坦预处理),ADM(22) -52)没有明显的心血管作用。相比之下,CGRP1受体拮抗剂CGRP(8-37)对LPS的降压以及肾和肠系膜血管舒张剂的作用产生了微小但显着的抑制作用,但在地塞米松和SB存在的情况下,仅在输注开始后6h 209670.结果表明,在这种内毒素血症模型中,在存在地塞米松和SB 209670的情况下观察到的明显区域性血管舒张不涉及ADM,但确实涉及CGRP,尽管程度很小。

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