Paulo Marcela Souza Lima, Souza Ingryd Fortes, Wandekoken Kethleen Gomes, Silva Karina Balestreiro, Dutra Jean Carlos Vencioneck, Freitas Josivany Valério de, Stegmiller Nataly Pescinalli, Pimassoni Lúcia Helena Sagrillo, Batitucci Maria do Carmo Pimentel, Paulo Danilo Nagib Salomão, Errera Flávia Imbroisi Valle
UFMG, Belo Horizonte, MG, Brazil.
EMESCAM, Vitoria, ES, Brazil.
Acta Cir Bras. 2015 Apr;30(4):264-9. doi: 10.1590/S0102-865020150040000005. Epub 2015 Apr 1.
To assess the mutagenic potential of the oxygen inhalation therapy (HBO), by means of the micronucleus test, performed in peripheral blood of rats that underwent subtotal splenectomy with lower pole preservation (ESTPI), after HBO sessions or simulations.
Eighteen male Wistar rats, were distributed into three groups of six animals: group 1 - submitted to ESTPI and HBO sessions; group 2 - submitted to ESTPI and HBO simulations; group 3 - underwent cyclophosphamide administration. In groups 1 and 2, blood samples from the animals' tails were collected before surgery (T0) and immediately after the 13th HBO session or simulation (T1). In group 3, tail blood samples were collected from animals before (T0) and 24 hours after (T1) cyclophosphamide (CP) delivery. The number of micronucleated normochromatic erythrocytes (MNNCE) was determined by blind counting 2000 normochromatic erythrocytes (NCE) per animal.
Micronuclei average after CP delivery in group 3 was higher than before its use, thus confirming the mutagenic activity of this drug (p=0.01). In groups 1 and 2, no significant difference in the average of Micronuclei was observed when comparing it to blood samples before and after the 13th HBO session or simulation.
The treatment protocol used in this study did not induce Micronucleus formation in animals submitted to ESTPI and HBO treatment or simulation.
通过微核试验评估在进行了保留脾下极的次全脾切除术(ESTPI)的大鼠外周血中,在接受高压氧治疗(HBO)疗程或模拟治疗后,HBO的诱变潜力。
18只雄性Wistar大鼠被分为三组,每组6只动物:第1组——接受ESTPI和HBO疗程;第2组——接受ESTPI和HBO模拟治疗;第3组——接受环磷酰胺给药。在第1组和第2组中,在手术前(T0)以及第13次HBO疗程或模拟治疗后立即(T1)采集动物尾巴的血样。在第3组中,在动物接受环磷酰胺(CP)给药前(T0)和给药后24小时(T1)采集尾巴血样。通过对每只动物的2000个正常染色红细胞(NCE)进行盲法计数来确定微核正常染色红细胞(MNNCE)的数量。
第3组中CP给药后的微核平均数高于给药前,从而证实了该药物的诱变活性(p = 0.01)。在第1组和第2组中,将第13次HBO疗程或模拟治疗前后的血样进行比较时,未观察到微核平均数有显著差异。
本研究中使用的治疗方案未在接受ESTPI和HBO治疗或模拟治疗的动物中诱导微核形成。