Sa-ardrit M, Thongtip N, Kornkaewrat K, Faisaikarm T, Kitiyanant Y, Mahasawangkul S, Pinyopummin A, Saikhun K
National Laboratory Animal Center, Mahidol University, Nakorn Pathom 73170, Thailand.
J S Afr Vet Assoc. 2009 Sep;80(3):146-50. doi: 10.4102/jsava.v80i3.192.
Knowledge about the acrosomal status of Asian elephant (Elephas maximus) sperm is extremely limited. The objective of this study was to evaluate the viability and acrosomal status of Asian elephant sperm following induction by calcium ionophore and heparin using propidium iodide (PI) and fluorescein isothiocyanate conjugated peanut agglutinin (FITC-PNA). Semen samples were collected from elephant bulls by manual stimulation. Semen was diluted with extender, cooled to 4 degrees C and transported to a laboratory for the experiment. Sperm cells were incubated in modified Tyrode's medium containing either 1 mM calcium ionophore or 10 mg/ml heparin for 5 h at 39 degrees C. Sperm recovered at the onset (0 h), 1, 2, 3, 4 and 5 h of incubation were simultaneously assessed for the viability and acrosomal status using dual staining of FITC-PNA and PI. Results were confirmed by transmission electron microscopy. A progressive increase in the proportion of live-acrosome reacted sperm was observed within 3 h of incubation in both treatment groups which slightly decreased at 4 to 5 h of incubation. At 1 to 3 h of incubation, the percentage of live-acrosome reacted sperm induced by calcium ionophore was higher (P < 0.05) than those induced by heparin and the control. However, there were no statistical differences at 4 to 5 h of incubation. A progressive reduction of the percentage of motile sperm was observed in the control as well as both treatment groups. Sperm motility decreased sharply when they were incubated in calcium ionophore compared with incubation in heparin and control groups. These results indicate that the occurrence of live-acrosome reacted sperm in the Asian elephant was induced by calcium ionophore at a rate higher than that induced by heparin.
关于亚洲象(Elephas maximus)精子顶体状态的知识极为有限。本研究的目的是使用碘化丙啶(PI)和异硫氰酸荧光素偶联花生凝集素(FITC-PNA)评估钙离子载体和肝素诱导后亚洲象精子的活力和顶体状态。通过手动刺激从雄象采集精液样本。精液用稀释液稀释,冷却至4摄氏度并运至实验室进行实验。将精子细胞在含有1 mM钙离子载体或10 mg/ml肝素的改良Tyrode培养基中于39摄氏度孵育5小时。在孵育开始时(0小时)、1、2、3、4和5小时回收的精子同时使用FITC-PNA和PI双重染色评估活力和顶体状态。结果通过透射电子显微镜得到证实。在两个处理组中,孵育3小时内观察到活的顶体反应精子比例逐渐增加,在孵育4至5小时时略有下降。在孵育1至3小时时,钙离子载体诱导的活的顶体反应精子百分比高于肝素和对照组诱导的(P < 0.05)。然而,在孵育4至5小时时没有统计学差异。在对照组以及两个处理组中均观察到活动精子百分比逐渐降低。与在肝素和对照组中孵育相比,精子在钙离子载体中孵育时活力急剧下降。这些结果表明,亚洲象中活的顶体反应精子的出现由钙离子载体诱导的速率高于肝素诱导的速率。