Hamilton J F, Morrison P F, Chen M Y, Harvey-White J, Pernaute R S, Phillips H, Oldfield E, Bankiewicz K S
Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892, USA.
Exp Neurol. 2001 Mar;168(1):155-61. doi: 10.1006/exnr.2000.7571.
Convection-enhanced delivery (CED) distributes macromolecules in the brain in a homogeneous, targeted fashion in clinically useful volumes. However, the binding of growth factors to heparin-binding sites in the extracellular matrix may limit the volume of distribution (V(d)). To overcome this limitation, we examined the effects of heparin coinfusion on V(d) of glial-derived neurotrophic factor (GDNF), neurturin (NTN), artemin, and a nonspecifically bound protein, albumin. Heparin coinfusion significantly enhanced the V(d) of GDNF and GDNF-homologous trophic factors, probably by binding and blocking heparin-binding sites in the extracellular matrix. Furthermore, coinfusion of heparin with NTN enhanced striatal dopamine metabolism, compared to trophic factor administered alone. The negligible benefit of GDNF in recent clinical trials of Parkinson's disease may result from limited tissue distribution. Heparin coinfusion during CED targeting the striatum may alleviate this important limitation. This study demonstrates the influence of receptor binding on the distribution of trophic factors in the CNS.
对流增强递送(CED)可将大分子以均匀、靶向的方式在临床上有用的体积内分布于脑内。然而,生长因子与细胞外基质中肝素结合位点的结合可能会限制分布体积(V(d))。为克服这一限制,我们研究了肝素共输注对胶质细胞源性神经营养因子(GDNF)、神经营养素(NTN)、Artemin以及一种非特异性结合蛋白白蛋白的V(d)的影响。肝素共输注显著提高了GDNF和GDNF同源营养因子的V(d),可能是通过结合并阻断细胞外基质中的肝素结合位点实现的。此外,与单独给予营养因子相比,肝素与NTN共输注可增强纹状体多巴胺代谢。在最近的帕金森病临床试验中,GDNF的益处微乎其微,可能是由于组织分布有限所致。在针对纹状体的CED过程中进行肝素共输注可能会缓解这一重要限制。本研究证明了受体结合对中枢神经系统中营养因子分布的影响。