Naloxone decreases tolerance to hypotensive, hypovolemic stress in healthy humans

Objective: In animal studies, naloxone, an opioid receptor antagonist, improves tolerance to hemorrhagic shock. The purpose of this study was to determine whether naloxone would augment tolerance to hypotensive hypovolemic stress (lower body negative pressure [LBNP]) in healthy human males. Design: This study was a repeated measures design. Setting: The experiments were conducted in a laboratory setting. Subjects: Eight healthy male subjects were tested. The subjects' ages were 30 ± 4.0 yrs, height = 177 ± 7.0 cm, and weight = 75.5 ± 3.5 kg (mean ± SEM). Interventions: Subjects underwent two LBNP exposures terminated by the onset of vasodepression. At each of the exposures, using a double‐blind procedure, the subjects received an intravenous injection of either saline placebo or naloxone in a dosage totaling 0.4 mg/kg. Measurements: Tolerance to the hypovolemic stress, heart rate, blood pressures, forearm blood flow, forearm vascular resistance were measured. Main Results: Naloxone reduced the tolerance to LBNP by 17%. Heart rate and blood pressure responses immediately before vasodepression were also attenuated by naloxone as compared with placebo. Forearm blood flow and vascular resistance were not altered by naloxone. Conclusion: Our results indicate that unlike animal models of hemorrhagic shock, blocking the opioid receptors in males reduced tolerance to a hypotensive hypovolemic stress.

[1]  M. Joyner,et al.  Vasovagal Syncope and Skeletal Muscle Vasodilatation: The Continuing Conundrum , 1997, Pacing and clinical electrophysiology : PACE.

[2]  K. Oldroyd,et al.  Role of endogenous opioids and catecholamines in vasovagal syncope. , 1996, European heart journal.

[3]  W. Armstead,et al.  Opioids contribute to hypoxia-induced pial artery dilation through activation of ATP-sensitive K+ channels. , 1995, The American journal of physiology.

[4]  J. Lightfoot,et al.  Quantification of tolerance to lower body negative pressure in a healthy population. , 1995, Medicine and science in sports and exercise.

[5]  M L Smith,et al.  Mechanisms of Vasovagal Syncope: Relevance to Postflight Orthostatic Intolerance , 1994, Journal of clinical pharmacology.

[6]  S. Fortney,et al.  Occurrence of presyncope in subjects without ventricular innervation. , 1993, Clinical science.

[7]  M. Carlson,et al.  Naloxone does not prevent vasovagal syncope during simulated orthostasis in humans. , 1993, Journal of the autonomic nervous system.

[8]  M. Thames,et al.  Neural Control Mechanisms and Vasovagal Syncope , 1993, Journal of cardiovascular electrophysiology.

[9]  H. Garan,et al.  Prospective evaluation of day-to-day reproducibility of upright tilt-table testing in unexplained syncope. , 1993, The American journal of cardiology.

[10]  N. Thakor,et al.  Presyncope caused by central hypovolaemia is not preceded by evoked potential alterations. , 1992, Clinical physiology.

[11]  E. Hasser,et al.  Sympathoinhibition and its reversal by naloxone during hemorrhage. , 1992, The American journal of physiology.

[12]  G. Pasternak,et al.  Pharmacological characterization of nalorphine, a kappa 3 analgesic. , 1991, The Journal of pharmacology and experimental therapeutics.

[13]  R. Strauss,et al.  Comparison of muscle sympathetic responses to hemorrhage and lower body negative pressure in humans. , 1991, Journal of applied physiology.

[14]  J. Kampine,et al.  Naloxone augments muscle sympathetic nerve activity during isometric exercise in humans. , 1991, The American journal of physiology.

[15]  B. Morgan,et al.  Vasovagal syncope after infusion of a vasodilator in a heart-transplant recipient. , 1990, The New England journal of medicine.

[16]  J. Holaday,et al.  The therapeutic efficacy of opiate antagonists in hemorrhagic shock. , 1989, Resuscitation.

[17]  C. Tankersley,et al.  Automated blood pressure measurements during exercise. , 1989, Medicine and science in sports and exercise.

[18]  J. Ludbrook,et al.  Intracisternal naloxone and cardiac nerve blockade prevent vasodilatation during simulated haemorrhage in awake rabbits. , 1989, The Journal of physiology.

[19]  J. Holaday,et al.  Evidence for a role of endorphins in the cardiovascular pathophysiology of primate shock. , 1988, Critical care medicine.

[20]  A. Faden,et al.  Opiate antagonists in traumatic shock , 1986 .

[21]  J. Schadt,et al.  Cardiovascular responses to hemorrhage and naloxone in conscious barodenervated rabbits. , 1986, The American journal of physiology.

[22]  L. Goldfrank,et al.  A dosing nomogram for continuous infusion intravenous naloxone. , 1986, Annals of emergency medicine.

[23]  L. Casey,et al.  Hemorrhagic hypotension increases plasma beta‐endorphin concentrations in the nonhuman primate , 1986, Critical care medicine.

[24]  E. Bernton Naloxone and TRH in the treatment of shock and trauma: what future roles? , 1985, Annals of emergency medicine.

[25]  J. Schadt,et al.  Endogenous opiate peptides may limit norepinephrine release during hemorrhage. , 1985, The Journal of pharmacology and experimental therapeutics.

[26]  Philip Smith,et al.  Efficacy and safety of naloxone in septic shock , 1985, Critical care medicine.

[27]  R. Gaddis,et al.  Presynaptic opiate receptor-mediated inhibition of endogenous norepinephrine and dopamine-beta-hydroxylase release in the cat spleen, independent of the presynaptic alpha adrenoceptors. , 1982, The Journal of pharmacology and experimental therapeutics.

[28]  T. Vargish,et al.  Naloxone without transfusion prolongs survival and enhances cardiovascular function in hypovolemic shock. , 1982, The Journal of pharmacology and experimental therapeutics.

[29]  W. Bunney,et al.  BEHAVIOURAL EFFECTS AFTER HIGH DOSE NALOXONE ADMINISTRATION TO NORMAL VOLUNTEERS , 1981, The Lancet.

[30]  A. M. Lefer,et al.  Protective actions of naloxone in hemorrhagic shock. , 1980, The American journal of physiology.

[31]  J. Holaday,et al.  Opiate antagonists: a role in the treatment of hypovolemic shock. , 1979, Science.

[32]  U. Freyschuss,et al.  The mechanism of orthostatic and haemorrhage fainting. , 1977, Scandinavian journal of clinical and laboratory investigation.

[33]  M. Jones NEW ROYAL AIR FORCE HOSPITAL IN CYPRUS. , 1963, Lancet.

[34]  S. Solomon,et al.  Principles of Physiology , 1950, The Yale Journal of Biology and Medicine.

[35]  T. Lewis A Lecture on VASOVAGAL SYNCOPE AND THE CAROTID SINUS MECHANISM , 1932, British medical journal.

[36]  T. Reisine Opioid analgesics and antagonists , 1996 .

[37]  N. Secher,et al.  Naloxone-provoked vaso-vagal response to head-up tilt in men , 1995, European Journal of Applied Physiology and Occupational Physiology.

[38]  S. Fortney,et al.  Repeatability and protocol comparability of presyncopal symptom limited lower body negative pressure exposures. , 1991, Aviation, space, and environmental medicine.

[39]  D. Glaister,et al.  Cerebral tissue oxygen status and psychomotor performance during lower body negative pressure (LBNP). , 1990, Aviation, space, and environmental medicine.

[40]  S. Fortney,et al.  Adaptation to repeated presyncopal lower body negative pressure exposures. , 1989, Aviation, space, and environmental medicine.

[41]  J. Ludbrook,et al.  Sympathoadrenal mechanisms in cardiovascular responses to naloxone after hemorrhage. , 1987, The American journal of physiology.

[42]  A. Faden,et al.  Opiate antagonist in traumatic shock. , 1986, Annals of emergency medicine.

[43]  M. Leider Goodman & Gilman's The Pharmacological Basis of Therapeutics , 1985 .

[44]  H. Kosterlitz,et al.  Classification of opioid receptors. , 1983, British medical bulletin.