1984
DOI: 10.1213/00000539-198401000-00005
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The Effect of Fentanyl on Arginine Vasopressin and Cortisol Secretion during Anesthesia

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1985
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Cited by 16 publications
(7 citation statements)
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“…Vasopressin is released into the circulation as a result of decreased baroreceptor activity during hypotensive or shock states and as a result of increases in plasma osmolality. 15 Pure µ-opioid receptor agonists may cause the release of vasopressin, 11,13 albeit the mechanism of vasopressin release under these circumstances is poorly understood. The increase in vasopressin concentrations could have been attributed to a direct action of remifentanil at µ-opiod receptors located in the CNS, 11 or it could have been a physiologic response 16 to the decrease in arterial blood pressure (associated with the decrease in CO) induced by remifentanil.…”
Section: Discussionmentioning
confidence: 99%
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“…Vasopressin is released into the circulation as a result of decreased baroreceptor activity during hypotensive or shock states and as a result of increases in plasma osmolality. 15 Pure µ-opioid receptor agonists may cause the release of vasopressin, 11,13 albeit the mechanism of vasopressin release under these circumstances is poorly understood. The increase in vasopressin concentrations could have been attributed to a direct action of remifentanil at µ-opiod receptors located in the CNS, 11 or it could have been a physiologic response 16 to the decrease in arterial blood pressure (associated with the decrease in CO) induced by remifentanil.…”
Section: Discussionmentioning
confidence: 99%
“…12 When administration of fentanyl (0.002 mg/kg, as an IV bolus) was compared with administration of halothane for maintaining anesthesia in humans receiving nitrous oxide and oxygen, the opioid caused an increase in plasma vasopressin concentrations that was blunted by prior administration of naloxone. 13 Vasopressin has vasoconstrictive properties mediated by activation of V 1 receptors within the vascular smooth muscles and may result in increased SVR, decreased CO, and decreased oxygen delivery. 14,15 The relationship between vasopressin release and opioid-induced changes in hemodynamic function has not been established.…”
mentioning
confidence: 99%
“…µ-agonist opioids can release vasopressin into the circulation, but the mechanism of this effect it not yet clear (HELLEBREKERS et al, 1989). Vasopressin acts on V1 receptors located in the smooth muscle cells of blood vessels to induce vasoconstriction, which increases systemic vascular resistance (LEHTINEN et al, 1984).…”
Section: Discussionmentioning
confidence: 99%
“…Acute increases in serum sodium levels can cause cerebral dehydration, potentially resulting into rupture of dural bridging veins, cerebral hemorrhages, venous sinus thrombosis, cerebral demyelination, and rhabdomyolysis [ 7 ]. There have been case reports wherein the use of certain anesthetic drugs was suspected to cause intraoperative polyuria, mainly including dexmedetomidine [ 8 15 ], ketamine [ 16 19 ], propofol [ 20 23 ], sevoflurane [ 24 , 25 ], remifentanil [ 26 ], and fentanyl [ 27 ]. A review paper published in the journal Anesthesia and Analgesia in 2021 reviewed 24 case reports of intraoperative polyuria due to anesthetic drugs and their possible mechanisms [ 2 ].…”
Section: Introductionmentioning
confidence: 99%