Murakami K, Hashimoto K, Kageyama Z, Takahara J, Ota Z
Nihon Naibunpi Gakkai Zasshi. 1983 Jul 20;59(7):983-92. doi: 10.1507/endocrine1927.59.7_983.
The effect of the synthetic ovine corticotropin-releasing factor (CRF) on adrenocorticotropin (ACTH) release was examined by the perifusion method using rat anterior pituitary tissue and rat monolayer cultured pituitary cells. Quartered anterior pituitaries were placed in a chamber and perifused at a rate of 400 microliters/min with Dulbecco's modified Eagle Medium (DMEM, pH 7.4) bubbled with a mixture of 95% O2 and 5% CO2. The perifused medium was fractionated, and the ACTH concentration was measured by radioimmunoassay. In the monolayer cultured pituitary cells, the amount of ACTH released in the culture medium during three hours incubation was assayed by radioimmunoassay. ACTH was released from the perifused anterior pituitary in a dose-related manner by the pulse administration of CRF or arginine vasopressin (AVP) at the concentration of 1 ng/ml, 10 ng/ml and 100 ng/ml. A significant difference was not found between CRF- and AVP-induced ACTH release. In the monolayer cultured pituitary cells, synthetic ovine CRF induced ACTH release in a dose-related manner between 30 pg/ml and 30 ng/ml, but AVP induced a slight ACTH release. ACTH release was pulsatile during the continuous administration of 2.5 ng/ml of CRF for 150 min, although if gradually increased during the continuous administration of 10 ng/ml or 20 ng/ml of CRF. The continuous administration of AVP also caused pulsatile ACTH release at 10 ng/ml, but the ACTH release gradually decreased during the continuous administration of AVP. The interaction between CRF and AVP on ACTH release was examined by two methods. When CRF and AVP were given simultaneously, a mainly additive effect on ACTH release was observed. However, a low concentration of CRF seemed to potentiate AVP-induced ACTH release. These results show that both CRF and AVP have a significant CRF activity on the perifusion system, that AVP induced a slight ACTH release in monolayer cultured pituitary cells, and that CRF acts additively or potently with AVP to control the ACTH release from the anterior pituitary gland.
采用大鼠垂体前叶组织和大鼠单层培养垂体细胞的灌流法,研究了合成的羊促肾上腺皮质激素释放因子(CRF)对促肾上腺皮质激素(ACTH)释放的影响。将四分的垂体前叶置于腔室中,以400微升/分钟的速度用含95% O2和5% CO2混合气体鼓泡的杜尔贝科改良伊格尔培养基(DMEM,pH 7.4)进行灌流。对灌流液进行分离,并通过放射免疫测定法测量ACTH浓度。在单层培养的垂体细胞中,通过放射免疫测定法测定孵育三小时期间培养基中释放的ACTH量。以1 ng/ml、10 ng/ml和100 ng/ml的浓度脉冲给予CRF或精氨酸加压素(AVP)时,ACTH以剂量相关的方式从灌流的垂体前叶释放。未发现CRF和AVP诱导的ACTH释放之间存在显著差异。在单层培养的垂体细胞中,合成的羊CRF在30 pg/ml至30 ng/ml之间以剂量相关的方式诱导ACTH释放,但AVP仅诱导轻微的ACTH释放。在持续给予2.5 ng/ml CRF 150分钟期间,ACTH释放呈脉冲式,尽管在持续给予10 ng/ml或20 ng/ml CRF期间ACTH释放逐渐增加。持续给予AVP在10 ng/ml时也会导致ACTH释放呈脉冲式,但在持续给予AVP期间ACTH释放逐渐减少。通过两种方法研究了CRF和AVP对ACTH释放的相互作用。当同时给予CRF和AVP时,观察到对ACTH释放主要有相加作用。然而,低浓度的CRF似乎增强了AVP诱导的ACTH释放。这些结果表明,CRF和AVP在灌流系统中均具有显著的CRF活性,AVP在单层培养的垂体细胞中诱导轻微的ACTH释放,并且CRF与AVP以相加或增强的方式控制垂体前叶ACTH的释放。