Kondratenko T Ia, Kuzina N V, Severin E S, Kornilova Z Kh, Perel'man M I
Vopr Med Khim. 1991 Jul-Aug;37(4):69-70.
Adrenergic receptors were studied in human lung parenchyma obtained from 10 patients with tuberculoma after segmental resection within the limits of surrounding normal tissues (controls) as well as from 10 patients with destructive pulmonary tuberculosis. Binding of alpha-adrenergic radioligand 3H-prazosin was saturable with high rate of affinity in lung parenchymal membranes of both normal tissues and tissues impaired with tuberculosis. The Scatchard analysis indicated that the affinity of 3H-prazosin binding was not altered in patients with tuberculosis, while amount of the ligand binding sites was significantly decreased as compared with control preparations (KD = 0.5 +/- 0.9 nM, Bmax = 273.5 +/- 59.9 fmol/mg in controls; KD = 0.5 +/- 0.07 nM, Bmax = 51.7 +/- 7.5 fmol/mg in tuberculous lung parenchyma). beta-Adrenergic and muscarinic acetylcholinergic receptors were studied in lung parenchyma of patients with tuberculosis. Binding parameters of beta-adrenergic ligand 3H-dihydroalprenolol and muscarinic antagonist 3H-quinuclidinyl benzylate were similar to those of control values. Amount of 3H-dihydroalprenolol binding sites was not markedly altered while content of 3H-prazosin binding sites was considerably decreased in lung parenchyma of patients with tuberculosis as compared with normal state. The data obtained suggest that population of alpha-adrenergic receptors was decreased in human lung parenchyma under conditions of destructive tuberculosis.
在10例结核瘤患者节段切除术后获取的周围正常组织(对照)以及10例毁损性肺结核患者的人肺实质中研究了肾上腺素能受体。α-肾上腺素能放射性配体3H-哌唑嗪在正常组织和结核损害组织的肺实质膜中均具有高亲和力的饱和结合。Scatchard分析表明,肺结核患者中3H-哌唑嗪结合的亲和力未改变,而与对照制剂相比,配体结合位点的数量显著减少(对照组中KD = 0.5±0.9 nM,Bmax = 273.5±59.9 fmol/mg;结核性肺实质中KD = 0.5±0.07 nM,Bmax = 51.7±7.5 fmol/mg)。在肺结核患者的肺实质中研究了β-肾上腺素能和毒蕈碱型乙酰胆碱能受体。β-肾上腺素能配体3H-二氢阿普洛尔和毒蕈碱拮抗剂3H-喹核醇基苯甲酸酯的结合参数与对照值相似。与正常状态相比,肺结核患者肺实质中3H-二氢阿普洛尔结合位点的数量没有明显改变,而3H-哌唑嗪结合位点的含量则显著降低。获得的数据表明,在毁损性肺结核情况下,人肺实质中α-肾上腺素能受体的数量减少。