Effects of Atropine, 2-PAM, or Pyridostigmine in Euvolemic or Hemorrhagic Conscious Swine.

Abstract

We investigated the effects of atropine, pralidoxime chloride (2-PAM), or pyridostigmine on the physiological and metabolic responses to hemorrhagic hypotension in conscious swine. All treatments were evaluated in euvolemic and hemorrhaged animals (36 ml of blood/kg/over one hour). Hemorrhage reduced blood pressure by 58 mmHg and decreased plasma acetylcholinesterase (AChE) activity by 18% in the control animals (n=6). Atropine injection increased heart rate similarly in hemorrhaged (n=6) and euvolemic (n=6) animals. Blood pressure was also transiently elevated following atropine administration. Injection of 2-PAM acutely elevated the levels of plasma lactate and plasma AChE, but values were similar to those in the untreated animals within 15 min in both euvolemic (n=7) and hemorrhaged (n=7) animals. Treatment with pyridostigmine for 3 days reduced plasma AChE by 37% and red blood cell AChE by 35% (n=12). Pretreatment with pridostigmine had no effect on any of the responses to hemorrhage. Posthemorrhage treatment with atropine or 2-PAM or pretreatment with pyridostigmine had no detrimental effects on the physiological or metabolic responses to moderate hemorrhage in conscious swine. Keywords: Wounds and injuries; Trauma.

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Document Details

Document Type
Technical Report
Publication Date
Apr 01, 1987
Accession Number
ADA181041

Entities

People

  • B. F. Williams
  • Charles E.W. Wade
  • D. S. Trail
  • G. D. Bonner
  • P. P. Waring

Organizations

  • Letterman Army Hospital

Tags

DTIC Thesaurus Topics

  • Acetylcholinesterases
  • Air Force
  • Air Force Facilities
  • Biological Sciences
  • Biomedical Research
  • Blood
  • Blood Cells
  • Blood Volume
  • Cardiovascular Physiological Phenomena
  • Chemical Warfare Agents
  • Heart Rate
  • Hemorrhage
  • Laboratory Animals
  • Medical Personnel
  • Military Personnel
  • Nerve Agents
  • Veins

Fields of Study

  • Medicine

Readers

  • Cardiovascular Physiology
  • Neurotoxicology