SURFACTANT PROTEIN A EXPRESSION IS DELAYED IN FETUSES OF STREPTOZOTOCIN-TREATED RATS

被引:20
作者
GUTTENTAG, SH
PHELPS, DS
STENZEL, W
WARSHAW, JB
FLOROS, J
机构
[1] HARVARD UNIV,SCH MED,DEPT PEDIAT,BOSTON,MA 02115
[2] YALE UNIV,SCH MED,NEW HAVEN,CT 06510
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1992年 / 262卷 / 04期
关键词
DIABETES; RESPIRATORY DISTRESS SYNDROME; PULMONARY SURFACTANT;
D O I
10.1152/ajplung.1992.262.4.L489
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The content and distribution of the 26-to 38-kDa surfactant protein (SP-A) and its mRNA were determined in fetuses of control and streptozotocin (STZ)-treated Sprague-Dawley rats using immunohistochemistry, RNA blotting, and in situ hybridization. Female rats were treated with 50 mg/kg STZ before mating, and the fetuses were killed at fetal days 18-21 or on neonatal days 1 and 2 (day of birth = end of day 22). SP-A was barely detectable on fetal day 18 in controls and easily detected by fetal day 21. In the STZ group, SP-A was decreased compared with controls at fetal days 18-21. However, by neonatal days 1-2, there were no significant differences in SP-A levels between groups. SP-A mRNA was detectable at fetal day 18 in controls, but it was decreased in the STZ group at day 18-21 (P < 0.02) and differences were no longer detected by neonatal days 1-2. SP-A and SP-A mRNA accumulated with advancing gestational age in both groups until neonatal days 1-2. The differences in SP-A and SP-A mRNA levels in the two groups diminished with advancing age but remained significant at fetal day 21. These data suggest that STZ-induced diabetes interferes with normal expression of SP-A in the developing fetal lung.
引用
收藏
页码:L489 / L494
页数:6
相关论文
共 31 条
[1]   SURFACE PROPERTIES IN RELATION TO ATELECTASIS AND HYALINE MEMBRANE DISEASE [J].
AVERY, ME ;
MEAD, J .
AMA JOURNAL OF DISEASES OF CHILDREN, 1959, 97 (05) :517-523
[2]   HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC ANALYSIS OF LUNG PHOSPHOLIPIDS AND THEIR PRECURSORS IN THE OFFSPRING OF DIABETIC RATS [J].
BOEHME, DS ;
ROBERTS, CM ;
BESSMAN, SP .
BIOCHEMICAL MEDICINE AND METABOLIC BIOLOGY, 1990, 44 (01) :29-36
[3]   MATURATION OF FETAL-RAT LUNG IN DIABETIC PREGNANCIES OF GRADUATED SEVERITY [J].
BOURBON, JR ;
PIGNOL, B ;
MARIN, L ;
RIEUTORT, M ;
TORDET, C .
DIABETES, 1985, 34 (08) :734-743
[4]   FETAL LUNG DEVELOPMENT IN THE DIABETIC PREGNANCY [J].
BOURBON, JR ;
FARRELL, PM .
PEDIATRIC RESEARCH, 1985, 19 (03) :253-267
[5]   PULMONARY SURFACTANT-ASSOCIATED PROTEIN-A ENHANCES THE SURFACE-ACTIVITY OF LIPID EXTRACT SURFACTANT AND REVERSES INHIBITION BY BLOOD PROTEINS INVITRO [J].
COCKSHUTT, AM ;
WEITZ, J ;
POSSMAYER, F .
BIOCHEMISTRY, 1990, 29 (36) :8424-8429
[6]   POSTNATAL STIMULATION OF RAT SURFACTANT PROTEIN-A SYNTHESIS BY DEXAMETHASONE [J].
FLOROS, J ;
PHELPS, DS ;
HARDING, HP ;
CHURCH, S ;
WARE, J .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 257 (02) :L137-L143
[7]   FETAL AND MATERNAL CORTICOSTERONE AND CORTICOSTEROID BINDING GLOBULIN IN THE DIABETIC RAT GESTATION [J].
GEWOLB, IH ;
WARSHAW, JB .
PEDIATRIC RESEARCH, 1986, 20 (02) :155-160
[8]   DELAYED PULMONARY MATURATION IN THE FETUS OF THE STREPTOZOTOCIN-DIABETIC RAT [J].
GEWOLB, IH ;
ROONEY, SA ;
BARRETT, C ;
INGELSON, LD ;
LIGHT, D ;
WILSON, CM ;
SMITH, GJW ;
GROSS, I ;
WARSHAW, JB .
EXPERIMENTAL LUNG RESEARCH, 1985, 8 (2-3) :141-151
[9]   DELAY IN PULMONARY GLYCOGEN DEGRADATION IN FETUSES OF STREPTOZOTOCIN DIABETIC RATS [J].
GEWOLB, IH ;
BARRETT, C ;
WILSON, CM ;
WARSHAW, JB .
PEDIATRIC RESEARCH, 1982, 16 (10) :869-873
[10]   INTERPRETATION AND SIGNIFICANCE OF LECITHIN-SPHINGOMYELIN RATIO IN AMNIOTIC-FLUID [J].
GLUCK, L ;
KULOVICH, MV ;
BORER, RC ;
KEIDEL, WN .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1974, 120 (01) :142-155