Dun Siok L, Brailoiu Eugen, Hsieh Wei-Kung, Lai Chih-Chia, Yang Jun, Chang Jaw Kang, Dun Nae J
Department of Pharmacology, Temple University School of Medicine, 3400 N. Broad Street, Philadelphia, PA 19140, USA.
Regul Pept. 2007 Apr 5;140(1-2):47-54. doi: 10.1016/j.regpep.2006.11.010. Epub 2006 Dec 21.
Cocaine- and amphetamine-regulated transcript (CART) peptide consists of a family of peptides. Expression of the peptide fragment CART(1-39) was explored in the rat using an antiserum directed against CART(1-39) of the short form of the human CART prohormone. CART(1-39)-immunoreactivity, herein referred to as irCART, was detected in the rat central and peripheral nervous tissues with a pattern similar to that labeled with the antiserum CART(55-102) or CART(79-102). For example, irCART cells were detected in the hypothalamus, pons, medulla oblongata, spinal cord, and adrenal medulla. In urethane-anesthetized rats, CART(1-39) (0.05 to 2 nmol) by intrathecal injection did not cause a significant change of blood pressure or heart rate, but potentiated the pressor effects of glutamate injected intrathecally. Lastly, the effect of CART(1-39) on intracellular calcium concentrations [Ca2+]i was assessed and compared to that caused by CART(55-102) in cultured rat cortical neurons using the microfluorimetric method. CART(1-39) (100 nM) induced two types of responses in a population of cortical neurons: 1) a slowly rising increase in [Ca2+]i superimposed with oscillations, and 2) a fast increase followed by a sustained increase of [Ca2+]i. CART(55-102) caused only a slowly rising increase in [Ca2+]i in cortical neurons. Our result shows that the expression pattern of irCART in the rat nervous system and the potentiating action of CART(1-39) on glutamate-induced pressor response is similar to that reported for CART(55-102); but the calcium mobilizing action of CART(1-39) differs from that of CART(55-102), suggesting the possible existence of multiple CART receptors coupled to different calcium signaling pathways.
可卡因和苯丙胺调节转录肽(CART)由一族肽组成。使用针对人CART前激素短形式的CART(1-39)的抗血清,在大鼠中研究了肽片段CART(1-39)的表达。在大鼠中枢和外周神经组织中检测到CART(1-39)免疫反应性,此处称为irCART,其模式与用抗血清CART(55-102)或CART(79-102)标记的模式相似。例如,在下丘脑、脑桥、延髓、脊髓和肾上腺髓质中检测到irCART细胞。在乌拉坦麻醉的大鼠中,鞘内注射CART(1-39)(0.05至2 nmol)不会引起血压或心率的显著变化,但会增强鞘内注射谷氨酸的升压作用。最后,使用微荧光法评估了CART(1-39)对培养大鼠皮质神经元细胞内钙浓度[Ca2+]i的影响,并与CART(55-102)引起的影响进行了比较。CART(1-39)(100 nM)在一群皮质神经元中诱导了两种类型的反应:1)[Ca2+]i缓慢上升并叠加振荡,2)快速上升后[Ca2+]i持续增加。CART(55-102)仅在皮质神经元中引起[Ca2+]i缓慢上升。我们的结果表明,大鼠神经系统中irCART的表达模式以及CART(1-39)对谷氨酸诱导的升压反应的增强作用与CART(55-102)报道的相似;但CART(1-39)的钙动员作用与CART(55-102)不同,这表明可能存在与不同钙信号通路偶联的多种CART受体。