Cox E, Cools V, Houvenaghel A
Laboratory of Veterinary Physiology, University of Antwerp, State University Centre, Belgium.
Vet Res Commun. 1989;13(2):159-70. doi: 10.1007/BF00346725.
In 45 newly-weaned 3 to 4-week-old piglets, diarrhoea was induced by a combined infection with transmissible gastroenteritis (TGE) virus and enterotoxigenic E. coli (ETEC) strains. In untreated control animals this dual inoculation resulted in profuse diarrhoea, vomiting, hypovolaemic shock and death of 77% of the animals within five days of TGE virus inoculation. Antisecretory drugs were administered intramuscularly for three consecutive days after experimental infection. The neurolepticum chlorpromazine, at 2 mg/kg/24 h, resulted in a significant inhibition of diarrhoea and vomiting, and in an increase in weight gain and survival. Sedation and hypothermia, however, were serious side-effects. The alpha 2 agonist clonidine, at 80 micrograms/kg/12 h, induced a significant antidiarrhoeal effect and a reduction in mortality. The drug, however, provoked decreased activity of alpha 2-adrenergic excitation and incoordination. The beta-adrenergic antagonist propranolol, at 0.33 mg/kg/8 h, and the calcium channel blocker verapamil, at 2 mg/kg/8 h, had no beneficial effect on the experimentally induced diarrhoea.
在45只3至4周龄刚断奶的仔猪中,通过接种传染性胃肠炎(TGE)病毒和产肠毒素大肠杆菌(ETEC)菌株引发腹泻。在未治疗的对照动物中,这种双重接种导致在接种TGE病毒后五天内出现大量腹泻、呕吐、低血容量性休克,77%的动物死亡。实验感染后连续三天肌肉注射抗分泌药物。氯丙嗪以2毫克/千克/24小时的剂量使用,可显著抑制腹泻和呕吐,并增加体重增加和存活率。然而,镇静和体温过低是严重的副作用。可乐定以80微克/千克/12小时的剂量使用,可产生显著的止泻作用并降低死亡率。然而,该药物会引发α2肾上腺素能兴奋活性降低和运动失调。普萘洛尔以0.33毫克/千克/8小时的剂量使用,以及维拉帕米以2毫克/千克/8小时的剂量使用,对实验性诱导的腹泻没有有益作用。