Effect of injection of antisense oligodeoxynucleotides of GAD isozymes into rat ventromedial hypothalamus on food intake and locomotor activity

被引:26
作者
Bannai, M
Ichikawa, M
Nishihara, M
Takahashi, M
机构
[1] Univ Tokyo, Dept Vet Physiol, Bunkyo Ku, Tokyo 113, Japan
[2] Tokyo Metropolitan Inst Neurosci, Dept Anat & Embryol, Tokyo, Japan
基金
日本学术振兴会;
关键词
antisense ODN; ventromedial hypothalamus; glutamic acid decarboxylase; GABA; food intake; locomotor activity;
D O I
10.1016/S0006-8993(97)01349-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the ventromedial hypothalamus (VMH), gamma-aminobutyric acid (GABA) plays a role in regulating feeding and running behaviors. The GABA synthetic enzyme, glutamic acid decarboxylase (GAD), consists of two isozymes, GAD(65) and GAD(67). In the present study, the phosphorothioated antisense oligodeoxynucleotides (ODNs) of each GAD isozyme were injected bilaterally into the VMH of male rats, and food intake, body weight and locomotor activity were monitored. ODNs were incorporated in the water-absorbent polymer (WAP, 0.2 nmol/mu l) so that ODNs were retained at the injection site. Each antisense ODN of GAD(65) or GAD(67) tended to reduce food intake on day 1 (day of injection = day 0) though not significantly. An injection combining both antisense ODNs significantly decreased food intake only on day 1, but body weight remained significantly lower than the control for 5 days. This suppression of body weight gain could be attributed to a significant increase in locomotor activity between days 3 and 5. Individual treatment with either ODNs did not change locomotor activity. The increase in daily locomotor activity in the group receiving the combined antisense ODNs occurred mainly during the light phase. Neither vehicle (WAP) nor control ODN affected food intake, body weight and locomotor activity. Histological studies indicated that antisense ODN distributed within 300 mu m from the edge of the area where WAP was located 24 h after the injection gradually disappeared within days, but still remained within 300 mu m distance even 7 days after the injection. Antisense ODN was effectively incorporated by all the cell types examined, i.e., neurons, astrocytes and microglias. Further, HPLC analysis revealed that antisense ODNs of GAD isozymes, either alone or combined, decreased the content of GABA by 50% in VMH 24 h after the injection. These results indicate that suppression of GABA synthesis by either of the GAD isozymes is synergistically involved in suppressing food intake and enhancing locomotor activity in rat VMH. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:305 / 315
页数:11
相关论文
共 33 条
[1]  
Akhtar S, 1992, Trends Cell Biol, V2, P139, DOI 10.1016/0962-8924(92)90100-2
[2]   HYPOTHALAMIC MAP OF STIMULATION CURRENT THRESHOLDS FOR INHIBITION OF FEEDING IN RATS [J].
BELTT, BM ;
KEESEY, RE .
AMERICAN JOURNAL OF PHYSIOLOGY, 1975, 229 (04) :1124-1133
[3]   HYPOTHALAMIC AND GENETIC OBESITY IN EXPERIMENTAL-ANIMALS - AUTONOMIC AND ENDOCRINE HYPOTHESIS [J].
BRAY, GA ;
YORK, DA .
PHYSIOLOGICAL REVIEWS, 1979, 59 (03) :719-809
[4]  
Eck S L, 1991, Curr Opin Biotechnol, V2, P897, DOI 10.1016/S0958-1669(05)80128-4
[5]   2 GENES ENCODE DISTINCT GLUTAMATE DECARBOXYLASES [J].
ERLANDER, MG ;
TILLAKARATNE, NJK ;
FELDBLUM, S ;
PATEL, N ;
TOBIN, AJ .
NEURON, 1991, 7 (01) :91-100
[6]   STIMULATION OF FOOD-INTAKE BY MUSCIMOL AND BETA-ENDORPHIN [J].
GRANDISON, L ;
GUIDOTTI, A .
NEUROPHARMACOLOGY, 1977, 16 (7-8) :533-536
[7]   2 FORMS OF THE GAMMA-AMINOBUTYRIC-ACID SYNTHETIC ENZYME GLUTAMATE-DECARBOXYLASE HAVE DISTINCT INTRANEURONAL DISTRIBUTIONS AND COFACTOR INTERACTIONS [J].
KAUFMAN, DL ;
HOUSER, CR ;
TOBIN, AJ .
JOURNAL OF NEUROCHEMISTRY, 1991, 56 (02) :720-723
[8]   BRAIN GLUTAMATE-DECARBOXYLASE CLONED IN LAMBDA-GT-11 - FUSION PROTEIN PRODUCES GAMMA-AMINOBUTYRIC-ACID [J].
KAUFMAN, DL ;
MCGINNIS, JF ;
KRIEGER, NR ;
TOBIN, AJ .
SCIENCE, 1986, 232 (4754) :1138-1140
[9]  
KELLY J, 1979, PHYSIOL BEHAV, V23, P1123, DOI 10.1016/0031-9384(79)90306-8
[10]   GABA STIMULATION AND BLOCKADE IN HYPOTHALAMUS AND MIDBRAIN - EFFECTS ON FEEDING AND LOCOMOTOR-ACTIVITY [J].
KELLY, J ;
ALHEID, GF ;
NEWBERG, A ;
GROSSMAN, SP .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1977, 7 (06) :537-541