EFFECTS OF CHRONIC HYPOXIA ON CAPILLARY-FLOW AND HEMATOCRIT IN RAT SKELETAL-MUSCLE

被引:13
作者
FISHER, AJ
SCHRADER, NW
KLITZMAN, B
机构
[1] DUKE UNIV, MED CTR, PLAST SURG RES LABS, BOX 3906, DURHAM, NC 27710 USA
[2] DUKE UNIV, MED CTR, DIV PHYSIOL, DURHAM, NC 27710 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1992年 / 262卷 / 06期
关键词
TISSUE OXYGENATION; RED CELL FLUX; RED CELL VELOCITY; MICROVESSEL LENGTH-DENSITY;
D O I
10.1152/ajpheart.1992.262.6.H1877
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The cremasteric microcirculation was studied in rats exposed to chronic hypoxia. Control male weanling Sprague-Dawley rats (n = 8) were raised for 42-49 days at 752 mmHg. Hypoxic rats (n = 9) were reared for 3 days at 551 mmHg, 4 days at 461 mmHg, 3 days at 371 mmHg, and 31-38 days at 311 mmHg (6,000 m). Red blood cells labeled with fluorescein isothiocyanate were injected. The exposed cremaster was observed using fluorescence microscopy. Rats acutely breathed 10, 21, and 30% O2 spontaneously in random order. Hypoxia-adapted animals had greater (P < 0.01) red cell flux (10.6 +/- 1.0 vs. 5.7 +/- 0.4/s), capillary hematocrits, capillary-to-systemic hematocrit ratios (0.42 +/- 0.02 vs. 0.33 +/- 0.02), and reduced red cell spacing (11.4 +/- 1.3 vs. 22.3 +/- 2.0-mu-m) than controls under 21% O2. Chronically hypoxic rats also demonstrated significantly (P < 0.05) larger capillary diameters (6.52 +/- 0.04 vs. 6.15 +/- 0.06-mu-m) and greater perfused (135 +/- 5 vs. 94 +/- 3 mm/mm3) and anatomic (182 +/- 5 vs. 151 +/- 8 mm/mm3) microvessel length-densities at 21% O2. Results were generally similar for 10 and 30% O2. Bulk capillary blood flow was significantly (P < 0.01) greater in controls (2.75 +/- 0.32 vs. 1.87 +/- 0.12 pl/s) only under 30% O2. Our experiments demonstrate that numerous physiological, in addition to anatomic, alterations can occur in the cremasteric microcirculation in response to chronic hypoxia.
引用
收藏
页码:H1877 / H1883
页数:7
相关论文
共 39 条
[1]   FAHRAEUS EFFECT IN NARROW CAPILLARIES (ID 3.3 TO 11.0 MU-M) [J].
ALBRECHT, KH ;
GAEHTGENS, P ;
PRIES, A ;
HEUSER, M .
MICROVASCULAR RESEARCH, 1979, 18 (01) :33-47
[2]   VASCULAR ISOLATION OF THE RAT CREMASTER MUSCLE [J].
ANDERSON, GL ;
ACLAND, RD ;
SIEMIONOW, M ;
MCCABE, SJ .
MICROVASCULAR RESEARCH, 1988, 36 (01) :56-63
[3]   OPEN CREMASTER MUSCLE PREPARATION FOR STUDY OF BLOOD-VESSELS BY IN-VIVO MICROSCOPY [J].
BAEZ, S .
MICROVASCULAR RESEARCH, 1973, 5 (03) :384-394
[4]  
BANCHERO N, 1975, P SOC EXP BIOL MED, V148, P435
[5]   CAPILLARY DEVELOPMENT DURING EXPOSURE TO CHRONIC HYPOXIA [J].
CASSIN, S ;
GILBERT, RD ;
BUNNELL, CE ;
JOHNSON, EM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1971, 220 (02) :448-&
[6]   MICRO-VASCULAR RAREFACTION IN SPONTANEOUSLY HYPERTENSIVE RAT CREMASTER MUSCLE [J].
CHEN, IIH ;
PREWITT, RL ;
DOWELL, RF .
AMERICAN JOURNAL OF PHYSIOLOGY, 1981, 241 (03) :H306-H310
[7]  
COKELET GR, 1982, MICROCIRCULATION, V2, P1
[8]  
DELANO FA, 1989, FASEB J, V3, pA1382
[9]   MICROVESSEL HEMATOCRIT - MEASUREMENT AND IMPLICATIONS FOR CAPILLARY OXYGEN-TRANSPORT [J].
DESJARDINS, C ;
DULING, BR .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 252 (03) :H494-H503
[10]   MICROVASCULAR RESPONSES TO ALTERATIONS IN OXYGEN-TENSION [J].
DULING, BR .
CIRCULATION RESEARCH, 1972, 31 (04) :481-+