Mustajoki P, Timonen K, Gorchein A, Seppäläinen A M, Matikainen E, Tenhunen R
Third Department of Medicine, University of Helsinki, Finland.
Eur J Clin Invest. 1992 Jun;22(6):407-11. doi: 10.1111/j.1365-2362.1992.tb01482.x.
The pathogenesis of the acute porphyric attack is not known. One hypothesis is that porphyrin precursors, especially 5-aminolaevulinic acid (ALA), are toxic for neuronal tissue. This was tested by infusing ALA in a male volunteer after a loading dose at a rate of 50-80 mg h-1 for 92.5 h. During the experiment plasma ALA concentration was 9-11 mumol 1-l and porphobilinogen concentration 3-6 mumol 1-l which are the levels seen during acute attacks. Urinary excretion of these porphyrin precursors was also markedly increased. ALA infusion caused no subjective symptoms and no change in pulse rate, blood pressure, or autonomic nerve function or conduction velocity of peripheral nerves. Photosensitivity was not demonstrable. It is concluded that sustained high plasma ALA concentration does not cause porphyria-like symptoms.
急性卟啉症发作的发病机制尚不清楚。一种假说认为,卟啉前体,尤其是5-氨基乙酰丙酸(ALA),对神经组织有毒性。通过在一名男性志愿者中给予负荷剂量后,以50-80mg h-1的速率输注ALA 92.5小时对此进行了测试。在实验期间,血浆ALA浓度为9-11μmol 1-l,胆色素原浓度为3-6μmol 1-l,这是急性发作期间所见的水平。这些卟啉前体的尿排泄也明显增加。输注ALA未引起主观症状,心率、血压、自主神经功能或周围神经传导速度也无变化。未表现出光敏性。结论是持续的高血浆ALA浓度不会引起卟啉症样症状。