Wilson M J, Norris H, Woodson M, Sinha A A, Estensen R D
VA Medical Center, Minneapolis, MN, USA.
Cell Mol Biol Res. 1995;41(6):603-12.
Pathology of the prostate gland in rats and humans is associated with aging. Our objective was to examine the effects of aging on the activities of plasminogen activators and metalloproteases in the prostatic complex of rats. Plasminogen activator activities (very low in the anterior, lateral, and dorsal lobes, in contrast to higher activities in the ventral lobe of 4-month-old adult rats) increased with aging in the dorsal and anterior prostate lobes of 31-month-old rats; these activities also increased in the dorsal and lateral lobes upon castration of 18-month-old rats. The plasminogen activator activities in the ventral lobe did not increase with aging to 18 months but did increase 3-5-fold after castration of either young or old rats. Metalloprotease activities of 70 and 76 kDa were observed in the anterior and lateral lobes of 4 month untreated adult rats, whereas the dorsal lobe showed MP of 70 and 92 kDa. Castration of young adult rats increased activities of all three molecular forms of metalloprotease in these three lobes. Increased expression of metalloprotease activities was also found with aging to 31 months in the anterior, lateral, and dorsal lobes. However, changes in metalloprotease activities associated with age were most striking in the lateral lobe and included activities of 52, 55, 81, 93, 113, and 117 kDa at 18 months of age. Castration for 30 days at this age resulted in a decline in the 52, 55, 113, and 117 kDa activities and an increase in activities of the 70, 81, and 93 kDa forms. These latter metalloprotease activities were also increased in the dorsal lobe after castration. Our results suggest that some metalloprotease activities increased in the dorsal lobe after castration. Our results suggest that some metalloprotease activities increased in the lateral lobe with age possibly result from an increased accumulation of secretory proteins (i.e., 52, 55, 113, and 117 kDa), whereas the 70, 81, and 93 kDa metalloprotease activities may be related to possible prostatitis and/or involved in changes in tissue organization. The increased expression of metalloprotease activities in the lateral and dorsal prostate lobes with aging, and castration upon aging, may be indicative of altered hormonal regulation of these proteases in these lobes.
大鼠和人类前列腺的病理学与衰老相关。我们的目的是研究衰老对大鼠前列腺复合体中纤溶酶原激活剂和金属蛋白酶活性的影响。纤溶酶原激活剂活性(在4个月大的成年大鼠中,前叶、侧叶和背叶中的活性非常低,与之形成对比的是腹叶中的活性较高)在31个月大的大鼠的背叶和前叶中随衰老而增加;在18个月大的大鼠去势后,背叶和侧叶中的这些活性也增加。腹叶中的纤溶酶原激活剂活性在18个月内不随衰老而增加,但在年轻或老年大鼠去势后增加3至5倍。在4个月未处理的成年大鼠的前叶和侧叶中观察到70 kDa和76 kDa的金属蛋白酶活性,而背叶显示有70 kDa和92 kDa的金属蛋白酶。年轻成年大鼠去势增加了这三个叶中所有三种分子形式的金属蛋白酶的活性。在前叶、侧叶和背叶中,随着年龄增长到31个月,金属蛋白酶活性的表达也增加。然而,与年龄相关的金属蛋白酶活性变化在侧叶中最为显著,在18个月大时包括52 kDa、55 kDa、81 kDa、93 kDa、113 kDa和117 kDa的活性。在这个年龄去势30天导致52 kDa、55 kDa、113 kDa和117 kDa活性下降,以及70 kDa、81 kDa和93 kDa形式的活性增加。去势后,背叶中这些后一种金属蛋白酶活性也增加。我们的结果表明,去势后背叶中一些金属蛋白酶活性增加。我们的结果表明,侧叶中随着年龄增长一些金属蛋白酶活性增加可能是由于分泌蛋白(即52 kDa、55 kDa、113 kDa和117 kDa)积累增加所致,而70 kDa、81 kDa和93 kDa金属蛋白酶活性可能与可能的前列腺炎和/或参与组织组织变化有关。随着衰老以及衰老时去势,侧叶和背叶中金属蛋白酶活性表达增加可能表明这些叶中这些蛋白酶的激素调节发生了改变。