Delivery of NGF to the Brain: Intranasal versus Ocular Administration in Anti-NGF Transgenic Mice

被引:54
作者
Capsoni, Simona [1 ,2 ]
Covaceuszach, Sonia [2 ]
Ugolini, Gabriele [2 ]
Spirito, Francesca [2 ]
Vignone, Domenico [1 ,2 ]
Stefanini, Barbara [2 ]
Amato, Gianluca [1 ,2 ]
Cattaneo, Antonino [1 ,3 ]
机构
[1] European Brain Res Inst, Fdn EBRI Rita Levi Montalcini, I-00143 Rome, Italy
[2] Lay Line Genom SpA, Rome, Italy
[3] SISSA, Int Sch Adv Studies, I-34014 Trieste, Italy
关键词
Alzheimer's disease; delivery; dosage; intranasal; nerve growth factor; non-invasive; ocular; pharmacokinetic; side effects; therapeutic window; NERVE GROWTH-FACTOR; FACTOR GENE-THERAPY; FOREBRAIN CHOLINERGIC NEURONS; ALZHEIMERS-DISEASE; NUCLEUS BASALIS; PRIMATE BRAIN; RETROGRADE TRANSPORT; MEMORY DEFICITS; TROPHIC FACTORS; ADULT;
D O I
10.3233/JAD-2009-0953
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Nerve growth factor (NGF) has a great potential for the treatment of Alzheimer's disease. However, the therapeutic administration of NGF represents a significant challenge, due to the difficulty to deliver relevant doses to the brain, in a safe and non-invasive way. We previously demonstrated the efficacy of a non-invasive delivery of NGF to the brain in animal models, by an intranasal route. Recently, topical eye application of NGF was proposed, as an option for the delivery of NGF to the brain. Here, we compare the efficacy of the two delivery routes of hNGF-61, a recombinant traceable form of human NGF, in the mouse neurodegeneration model AD11. The intranasal administration appeared to be significantly more effective than the ocular one, in rescuing the neurodegenerative phenotypic hallmarks in AD11 mice. The ocular administration of hNGF-61 showed a more limited efficacy, even at higher doses. Thus, NGF nasal drops represent a viable and effective option to successfully deliver therapeutic NGF to the brain in a non-invasive manner.
引用
收藏
页码:371 / 388
页数:18
相关论文
共 71 条
[1]   Stress and nerve growth factor - Findings in animal models and humans [J].
Aloe, L ;
Alleva, E ;
Fiore, M .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2002, 73 (01) :159-166
[2]  
Alzheimer A., 1907, Allg Zietschr Psychiatr Psychiatr-Gerichtl Med, V64, P146, DOI DOI 10.1002/CA.980080612
[3]   THE CHOLINERGIC HYPOTHESIS OF GERIATRIC MEMORY DYSFUNCTION [J].
BARTUS, RT ;
DEAN, RL ;
BEER, B ;
LIPPA, AS .
SCIENCE, 1982, 217 (4558) :408-417
[4]   Testosterone, but not nonaromatizable dihydrotestosterone, improves working memory and alters nerve growth factor levels in aged male rats [J].
Bimonte-Nelson, HA ;
Singleton, RS ;
Nelson, ME ;
Eckman, CB ;
Barber, J ;
Scott, TY ;
Granholm, ACE .
EXPERIMENTAL NEUROLOGY, 2003, 181 (02) :301-312
[5]   Regulated lentiviral NGF gene transfer controls rescue of medial septal cholinergic neurons [J].
Blesch, A ;
Conner, J ;
Pfeifer, A ;
Gasmi, M ;
Ramirez, A ;
Britton, W ;
Alfa, R ;
Verma, I ;
Tuszynski, MH .
MOLECULAR THERAPY, 2005, 11 (06) :916-925
[6]   ASSOCIATION BETWEEN QUANTITATIVE MEASURES OF DEMENTIA AND OF SENILE CHANGE IN CEREBRAL GREY MATTER OF ELDERLY SUBJECTS [J].
BLESSED, G ;
TOMLINSON, BE ;
ROTH, M .
BRITISH JOURNAL OF PSYCHIATRY, 1968, 114 (512) :797-+
[7]   Chronic nerve growth factor administration increases the peripheral exocytotic activity of capsaicin-sensitive cutaneous neurons [J].
Bowles, Walter R. ;
Sabino, Ma'Lou ;
Harding-Rose, Catherine ;
Hargreaves, Kenneth M. .
NEUROSCIENCE LETTERS, 2006, 403 (03) :305-308
[8]   Nerve growth factor treatment enhances release of immunoreactive calcitonin gene-related peptide but not substance P from spinal dorsal horn slices in rats [J].
Bowles, WR ;
Sabino, ML ;
Harding-Rose, C ;
Hargreaves, KM .
NEUROSCIENCE LETTERS, 2004, 363 (03) :239-242
[9]   β-amyloid plaques in a model for sporadic Alzheimer's disease based on transgenic anti-nerve growth factor antibodies [J].
Capsoni, S ;
Giannotta, S ;
Cattaneo, A .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2002, 21 (01) :15-28
[10]   Alzheimer-like neurodegeneration in aged antinerve growth factor transgenic mice [J].
Capsoni, S ;
Ugolini, G ;
Comparini, A ;
Ruberti, F ;
Berardi, N ;
Cattaneo, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (12) :6826-6831