Increased nerve growth factor mRNA in lateral calf skin biopsies from diabetic patients

被引:26
作者
Diemel, LT [1 ]
Cai, F [1 ]
Anand, P [1 ]
Warner, G [1 ]
Kopelman, PG [1 ]
Fernyhough, P [1 ]
Tomlinson, DR [1 ]
机构
[1] Queen Mary Univ London, Dept Pharmacol, London E1 4NS, England
关键词
diabetes mellitus; human; neuropathy; nerve growth factor; neurotrophin; cRT-PCR;
D O I
10.1046/j.1464-5491.1999.00035.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims This study set out to establish a novel procedure for the measurement of human nerve growth factor (NGF) messenger ribonucleic acid (mRNA) and to use this method to measure NGF expression in skin biopsies from control subjects and from patients with early neuropathies. NGF mRNA levels were related to functional measures of the competence of NGF-responsive nerves. Methods mRNA levels were measured by competitive reverse transcription with polymerase chain reaction amplification (cRT-PCR). Functional correlates of this observation were assessed by indices of thermal sensitivity - mediated by C-fibres, whose phenotype is regulated by NGF. Results NGF mRNA was increased in skin biopsies from 19 diabetic patients (5.12+/-3.88 (sD)) compared with samples from eight controls (1.57+/-0.95; P=0.001). Diabetic patients showed significantly (P<0.001) diminished detection of cool and warm stimuli compared to age matched control group (n=24), but there were no differences in detection of heat as pain, or correlation with NGF mRNA levels. Conclusions These findings suggest abnormally increased expression of NGF in diabetic neuropathy, which may represent a compensatory mechanism for impaired phenotype in NGF-responsive neurones.
引用
收藏
页码:113 / 118
页数:6
相关论文
共 46 条
[1]   NERVE GROWTH-FACTOR IN THE SYNOVIAL-FLUID OF PATIENTS WITH CHRONIC ARTHRITIS [J].
ALOE, L ;
TUVERI, MA ;
CARCASSI, U ;
LEVIMONTALCINI, R .
ARTHRITIS AND RHEUMATISM, 1992, 35 (03) :351-355
[2]  
Amand DS, 1996, DNA CELL BIOL, V15, P415
[3]   NERVE GROWTH-FACTOR LEVELS IN CULTURED HUMAN SKIN CELLS - EFFECT OF GESTATION AND VIRAL TRANSFORMATION [J].
ANAND, P ;
FOLEY, P ;
NAVSARIA, HA ;
SINICROPI, D ;
WILLIAMSCHESTNUT, RE ;
LEIGH, IM .
NEUROSCIENCE LETTERS, 1995, 184 (03) :157-160
[4]   The role of endogenous nerve growth factor in human diabetic neuropathy [J].
Anand, P ;
Terenghi, G ;
Warner, G ;
Kopelman, P ;
WilliamsChestnut, RE ;
Sinicropi, DV .
NATURE MEDICINE, 1996, 2 (06) :703-707
[5]   NERVE GROWTH-FACTOR ADMINISTRATION PROTECTS AGAINST EXPERIMENTAL DIABETIC SENSORY NEUROPATHY [J].
APFEL, SC ;
AREZZO, JC ;
BROWNLEE, M ;
FEDEROFF, H ;
KESSLER, JA .
BRAIN RESEARCH, 1994, 634 (01) :7-12
[6]   DIABETIC NEUROPATHIES AND PAIN [J].
BOULTON, AJM ;
WARD, JD .
CLINICS IN ENDOCRINOLOGY AND METABOLISM, 1986, 15 (04) :917-931
[7]   DIABETIC NEUROPATHY, NERVE GROWTH-FACTOR AND OTHER NEUROTROPHIC FACTORS [J].
BREWSTER, WJ ;
FERNYHOUGH, P ;
DIEMEL, LT ;
MOHIUDDIN, L ;
TOMLINSON, DR .
TRENDS IN NEUROSCIENCES, 1994, 17 (08) :321-325
[8]   EXPRESSION OF NEUROTROPHIN GENES IN HUMAN FIBROBLASTS - DIFFERENTIAL REGULATION OF THE BRAIN-DERIVED NEUROTROPHIC FACTOR GENE [J].
CARTWRIGHT, M ;
MIKHEEV, AM ;
HEINRICH, G .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 1994, 12 (08) :685-693
[9]   A RAPID AND VERSATILE METHOD TO SYNTHESIZE INTERNAL STANDARDS FOR COMPETITIVE PCR [J].
CELI, FS ;
ZENILMAN, ME ;
SHULDINER, AR .
NUCLEIC ACIDS RESEARCH, 1993, 21 (04) :1047-1047
[10]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2