Diabetic rat testes: morphological and functional alterations

被引:87
作者
Ricci, G. [1 ,2 ]
Catizone, A. [3 ]
Esposito, R. [1 ,2 ]
Pisanti, F. A. [4 ]
Vietri, M. T. [5 ]
Galdieri, M. [1 ,2 ]
机构
[1] Univ Naples 2, Dept Expt Med, Histol & Embryol Lab, Sch Med, I-80138 Naples, Italy
[2] Natl Inst Biostruct & Biosyst Interuniv Consortiu, Unit Sect Naples, Naples, Italy
[3] Univ Roma La Sapienza, Dept Histol & Med Embryol, Sch Med, Rome, Italy
[4] Univ Calabria, Dept Cell Biol, Sch Biol Sci, I-87036 Cosenza, Italy
[5] Univ Naples 2, Dept Gen Pathol, Sch Med, I-80138 Naples, Italy
关键词
Blood-testis barrier; diabetic syndrome; oxidative stress; testis; testosterone; STREPTOZOTOCIN-INDUCED HYPERGLYCEMIA; TIGHT JUNCTION DYNAMICS; OXIDATIVE STRESS; CADMIUM CHLORIDE; SEXUAL-BEHAVIOR; SPERMATOGENESIS; APOPTOSIS; BARRIER; DYSFUNCTION; SPERM;
D O I
10.1111/j.1439-0272.2009.00937.x
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
P>Reproductive dysfunction is a consequence of diabetes, but the underlying mechanisms are poorly understood. This study investigated the histological and molecular alterations in the testes of rats injected with streptozotocin at prepuperal (SPI rats) and adult age (SAI rats) to understand whether diabetes affects testicular tissue with different severity depending on the age in which this pathological condition starts. The testes of diabetic animals showed frequent abnormal histology, and seminiferous epithelium cytoarchitecture appeared altered as well as the occludin distribution pattern. The early occurrence of diabetes increased the percentage of animals with high number of damaged tubules. The interstitial compartment of the testes was clearly hypertrophic in several portions of the organs both in SPI and SAI rats. Interestingly, fully developed Leydig cells were present in all the treated animals although abnormally distributed. Besides the above-described damages, we found a similar decrease in plasma testosterone levels both in SPI and SAI rats. Oxidative stress (OS) is involved in the pathogenesis of various diabetic complications, and in our experimental models we found that manganese superoxide dismutase was reduced in diabetic animals. We conclude that in STZ-induced diabetes, the altered spermatogenesis, more severe in SPI animals, is possibly due to the effect of OS on Leydig cell function which could cause the testosterone decrease responsible for the alterations found in the seminiferous epithelium of diabetic animals.
引用
收藏
页码:361 / 368
页数:8
相关论文
共 25 条
[1]   Apoptotic germ-cell death and testicular damage in experimental diabetes: prevention by endothelin antagonism [J].
Cai, L ;
Chen, SL ;
Evans, T ;
Deng, DX ;
Mukherjee, K ;
Chakrabarti, S .
UROLOGICAL RESEARCH, 2000, 28 (05) :342-347
[2]   HYPOTHALAMIC-HYPOPHYSEAL-GONADAL AXIS IN THE STREPTOZOTOCIN-INDUCED DIABETIC MALE-RAT [J].
CALVO, JC ;
BARANAO, JL ;
TESONE, M ;
CHARREAU, EH .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1984, 20 (03) :769-772
[3]   Aging alters the functional expression of enzymatic and non-enzymatic anti-oxidant defense systems in testicular rat Leydig cells [J].
Cao, LC ;
Leers-Sucheta, S ;
Azhar, S .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2004, 88 (01) :61-67
[4]   Hepatocyte growth factor modulates Sertoli-Sertoli tight junction dynamics [J].
Catizone, A. ;
Ricci, G. ;
Galdieri, M. .
JOURNAL OF CELLULAR PHYSIOLOGY, 2008, 216 (01) :253-260
[5]   Is cadmium chloride-induced inter-sertoli tight junction permeability barrier disruption a suitable in vitro model to study the events of junction disassembly during spermatogenesis in the rat testis? [J].
Chung, NPY ;
Cheng, CY .
ENDOCRINOLOGY, 2001, 142 (05) :1878-1888
[6]  
De Young L, 2004, J ANDROL, V25, P830
[7]  
FICHER M, 1984, J ANDROL, V5, P8
[8]   H2O2 at physiological concentrations modulates Leydig cell function inducing oxidative stress and apoptosis [J].
Gautam, DK ;
Misro, MM ;
Chaki, SP ;
Sehgal, N .
APOPTOSIS, 2006, 11 (01) :39-46
[9]   EFFECT OF CADMIUM CHLORIDE ON TRANSEPITHELIAL ELECTRICAL-RESISTANCE OF SERTOLI-CELL MONOLAYERS IN 2-COMPARTMENT CULTURES - A NEW MODEL FOR TOXICOLOGICAL INVESTIGATIONS OF THE BLOOD-TESTIS BARRIER INVITRO [J].
JANECKI, A ;
JAKUBOWIAK, A ;
STEINBERGER, A .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1992, 112 (01) :51-57
[10]   Streptozotocin-induced diabetes increases apoptosis through JNK phosphorylation and Bax activation in rat testes [J].
Koh, Phil-Ok .
JOURNAL OF VETERINARY MEDICAL SCIENCE, 2007, 69 (09) :969-971