Garner A, Flemström G
Am J Physiol. 1978 Jun;234(6):E535-41. doi: 10.1152/ajpendo.1978.234.6.E535.
Measurement of gastric intraluminal PCO2 and pH in the anesthetized guinea pig enabled simultaneous determination of total H+ and HCO3- gastric secretions. There was quantitative agreement between the release of CO2 and decrease in HCO3- after intragastric instillation of HCl. The basal rate of HCO3- secretion (approximately 40 mueq-h-1) was, in most cases, smaller than spontaneous H+ secretion, but gastric net secretory output was alkaline (HCO3- greater than H+) after inhibition of acid secretion with histamine H2-receptor antagonists (cimetidine 20 mg-kg-1 or metiamide 35 mg-kg-1). Carbachol (1-2 microgram-kg-1) stimulated secretion of both HCO3- and H+; only the latter response was sensitive to the histamine antagonists. Atropin (100 microgram-kg-1) blocked stimulation of HCO3- secretion but did not affect the basal output of HCO3-. An increase in HCO3- secretion was associated with an equivalent increase in net Na+ influx and an increase in the net influx of Cl- with H+ plus K+. Intragastric neutralization of H+ by HCO3- is likely to occur at the mucosal surface and may protect the mucosa from the damaging effects of intraluminal acid.
对麻醉的豚鼠胃腔内PCO₂和pH值的测量能够同时测定胃中H⁺和HCO₃⁻的总分泌量。胃内注入HCl后,CO₂释放量与HCO₃⁻减少量之间存在定量一致性。在大多数情况下,HCO₃⁻的基础分泌速率(约40μeq·h⁻¹)小于自发的H⁺分泌速率,但在用组胺H₂受体拮抗剂(西咪替丁20mg·kg⁻¹或甲硫咪特35mg·kg⁻¹)抑制胃酸分泌后,胃的净分泌量呈碱性(HCO₃⁻>H⁺)。卡巴胆碱(1 - 2μg·kg⁻¹)刺激HCO₃⁻和H⁺的分泌;只有后者的反应对组胺拮抗剂敏感。阿托品(100μg·kg⁻¹)阻断了HCO₃⁻分泌的刺激,但不影响HCO₃⁻的基础分泌量。HCO₃⁻分泌的增加与净Na⁺内流的等量增加以及Cl⁻与H⁺加K⁺的净内流增加有关。HCO₃⁻对胃内H⁺的中和作用可能发生在黏膜表面,并可能保护黏膜免受腔内酸的损伤作用。