CC BY
35
gested carbohydrates. No significant difference between the indices of triglyceride level in the alveolar bone and the gum tissue in the 3r group animals was found (Р3,1>0,01-0,05) compared to the corresponding indices in the 1st group animals. Conclusions. The level of triglycerides in the periodontal tissues of the experimental animals depends on the food ration. When keeping animals on unbalanced vegetable fat ration the signs of insulin resistance in the periodontal tissues are detected to be increased. The unbalanced animal fat ration does not affect the studied tissues.
UDC 612.392.4:612.419]:612.223 Filimonov V., Burega I.
FEATURES OF HUMORAL REGULATION MECHANISM OF IRON DELIVERY TO THE BONE MARROW IN CONDITION OF HYPOXIC HYPOXIA ACTION
Zaporizhzhya State Medical University, Zaporizhzhya
Iron is necessary to each organism. Ability of this transition metal exists in two redox conditions makes it useful in catalytic center of the primary biochemical reactions. DNA synthesis, transporting of oxygen and electrons and respiration require the iron. The same qualities, that make the iron useful in each of these reactions, make it toxic. Free iron has the ability to generate the oxidative radicals that damage the main biological compounds such as lipids, proteins and DNA. Humans iron metabolism is characterized by regulation of reabsorption and excretion of iron's quantity. Inadequate responses or the absence of responses lead to anemia or iron overload. Until that time, the mechanism and regulatory factors that provide process of iron metabolism regulation in organism and sufficient delivery of iron to the bone marrow for synthetic processes, is not clearly established. The question about realization of feedback between hematopoiesis in the bone marrow and iron delivery system for providing adequate synthesis of hemoglobin by erythroid elements remains one of the unsolved problems of classic hematology. Object. To determine the influence of thin humoral factors of iron metabolism in rats after hypoxic hypoxia action. Methods. Studies were done on 166 white laboratory male rats. Animals were divided into 5 groups: the 1st group - intact rats (I); the 2d group -the rats - donors of blood serum (D), were placed into the hypoxia chamber and undergo of hypoxic hypoxia action during 18 hours, barometric and oxygen partial pressure in the hypoxia chamber corresponded with notional "height" to 4,000 meters above sea level; the 3 d group - rats-recipients 1of blood serum (R1), which were introduced intramuscularly 2 ml of blood serum of the 2 animals group, the 4th group - rats-recipients 2 (R2), which were introduced intramuscularly 2 ml of blood serum of the 3 animals group; the 5th group -control (C), animals were placed into the hypoxia chamber without changes of barometric and partial pressure and were introduced intramuscularly 2 ml of physiological solution. To determine the influence of thin humoral factors of iron metabolism in rats after hypoxic hypoxia action the whole blood and serum were studied. Laboratory clinical tests, biochemical and statistical methods to determine reticulocytes, erythrocytes, hemoglobin quantity and hematocrit, indicators of iron serum, total iron binding capacity (TIBC) and unsaturated iron binding capacity (UIBC) were used. Results. On the 1st day after 18 hours of the animals' staying under hypoxic hypoxia conditions the increase quantity of reticulocytes were detected. The indicators of blood serum iron transport were decreased except indicators of UIBC. In the studies of animals - recipients 1, with erythropoietin' absence in their blood serum, were determined that in the group of animals - recipients 2 indicators of total iron and transferrin saturation were twice bigger in comparison with control group. On the 5th day, the indicators of total iron and transferrin saturation were decreased relatively to the 3 day, but were increased relatively to the control group. On the 7th day total iron, TIBC, UIBC and transferrin saturation return to norm and did not differ in all groups. Conclusions. Thus, during activation of erythropoiesis the increasing delivery of iron to the bone marrow is not stimulated by erythropoietin. Researches showed, that under the action of this hormone the conditional factor of a thin humoral regulation is participating in one of the stages of stimulation of iron mobilization was formed.
Key words: erythrocytes, reticulocytes, iron, anoxia, rats.
Work is a fragment of the research work of the Department of Normal Physiology of Zaporizhzhya State Medical University «Researches of iron metabolism mechanisms in conditions of erythropoiesis stimulation and oppression», State Registration № 0107U005121.
Iron is essential for living organisms. This transition of the metal exists in two redox conditions, which make it useful in catalytic center of the primary biochemical reactions. DNA synthesis, transporting of oxygen and electrons, and respiration require the iron. The same qualities, that make the iron useful in each of these reactions, make it toxic. Free iron has the ability to generate the oxidative radicals that
Inroduction
damage the main biological compounds such as lipids, proteins and DNA. Human body iron metabolism is characterized by balance between re-absorption and excretion of iron quantity. Inadequate responses or their absence lead to anemia or iron overload [8]. Recently, much attention of physiologists, pathophysiologists and clinicians has been paid to the issue on iron homeostasis regulation that is an important process for normal organism functioning. Iron
metabolic disorders, its deficiency or excessive amount determine a pathogenesis of most diseases [2]. Iron regulation disorders, whether they are hereditary or acquired, lead to iron deficiency in organism and can cause severe diseases. Shortage of iron due to poor dietary intake results in iron deficiency anemia (IDA) [7,9], and this problem remains urgent for medicine despite great progress in diagnosis and treatment of IDA. Activity of all proteins that participate in iron metabolism is strictly regulated that enables to maintain iron homeostasis [1]. Nevertheless, the mechanism and regulatory factors that provide iron metabolism regulation in organism and sufficient iron delivery to the bone marrow for synthetic processes, is still unclear. The question about realization of feedback between bone marrow hematopoiesis and iron delivery system for providing adequate synthesis of hemoglobin by erythroid elements remains one of the unsolved problems of classic hematology.
Object: to determine the influence of fine humoral factors of iron metabolism in rats exposed to hypoxic hypoxia.
Materials and methods
Studies were carried out on 166 white laboratory male rats. Animals were divided into 5 groups: the 1st group involved intact rats (I). The 2d group included rats who were donors of blood serum (D). They were placed into the hypoxia chamber and underwent hypoxic hypoxia during 18 hours, barometric and oxygen partial pressure in the hypoxia chamber corresponded to notional "height" of 4000 meters above sea level. The 3rd group involved rats-recipients 1 of blood serum (R1), who were administered 2 ml of blood serum taken from the animals of the 2d group, intramuscularly; the 4th group included rats-recipients 2 (R2), who were introduced intramuscularly 2 ml of blood serum taken from the animals of the 3rd group; the 5th group was control (C) and made up of animals placed into the hypoxia chamber without changes of barometric and partial pressure. These animals were introduced 2 ml of physiological solution intramuscularly. Keeping the animals and their involving into experiments were carried out according to the regulations of European convention on the protection of vertebrata', which are used for experimental and other scientific purposes (Strasbourg, 18.03.86), the low of Ukraine "Animal Protection from Cruel Appeal" (№ 1759 from 15.09.2009). The killing and further taking the material from the animals of the 2d, 3rd, 5th groups were done on the 1st and 3rd days after exposure to hypoxia, and in animals of 4th group on the 3rd, 5th, 7th days. The parameters we evaluated in the study were the following: the reticulocytes quantity by the standard kit ReticuloFarb "Filisit" (Ukraine); the red blood cells (RBC), hemoglobin amount and hematocrit were
assayed by the haematology analyzer MYTHIC 18 (France); iron serum was assessed by the kit Zalizo Prestige 24i "CORMEY"(Poland); total iron binding capacity (TIBC), unsaturated iron binding capacity (UIBC), percentage of transferrin saturation (TS) were evaluated by the kit Zalizozv'yazuyuchya zdatnist' Prestige 24i "CORMEY" (Poland) in an automatic biochemical analyzer PRESTIGE 24i (Japan). Processing of the obtained numerical results was conducted
through statistical methods - STATISTICA® for Windows 6.1 (StatSoft Inc., № AXXR712D833214FAN5). The difference between the variables was considered statistically significant at the p < 0,05.
Results
On the 1st day after hypoxia chamber action the amount of erythrocytes, hemoglobin, hematocrit and blood serum unsaturated iron -binding capacity in the donors of experimental group animals did not differ from the findings demonstrated by the animals of intact and control groups (tabl. 1). The reticulocytes were significantly increased (26,1±2,2) compared with the 1st and 5th groups (18,2±0,7; 18,4±0,8 accordingly). Indicators of serum iron (24,2±0,9), blood serum total iron binding capacity (44,3±1,1) and percentage of transferrin saturation (55,7±2,7) were significantly decreased compared with intact and control groups (tabl. 1). During the experiment the indices of peripheral blood and blood serum iron - transport function in the animals of intact group did not significantly differ from the indices in the control group (tabl. 1). On the 3rd day after hypoxic hypoxia action, in animals of the 2d experimental group the erythrocytes, hemoglobin and hematocrit indicators did not differ from those indices in the 1st and 5thgroups (tabl. 1). The reticulocytes were significantly increased (41,1±0,7) compared with rats on the 1st day in the 2d experimental group (26,1±0,9) and intact group (18,2±0,7). In rats of the 2d experimental group the total blood serum of iron was increased (44,6±1,2) in comparison with intact group - (32,4±0,9). Blood serum TIBC of experimental animals significantly higher (79,3±1,8) than indicators of intact group (47,6±1; p< 0,05). Blood serum UIBC of the 2d experimental group greatly increased (31,2±1,4) relatively to the control (15,1±1). Transferrin saturation indicator of experimental group is less (52,3±2,8) than control indicators (68,2±2,2). On the 1st day after injection of animals - donors' blood serum in rats' recipients 1 the reticulocytes quantity is significantly increased (39,1±0,6) in comparison with control and intact groups (18,7±0,7; 18,2±0,7). Hematocrit and quantity indicators of erythrocytes and hemoglobin do not differ from the same parameters of the 1st and 5th groups (tabl. 2).
Table 1
Indicators of rats (donors) peripheral blood and iron-transport function (n=6)
Intact Control Experiment
1 day 3 day 1 day 3 day
Reticulocytes (%о) 18,2±0,7 18,4±0,8 17,6±0,6 26,1±0,9H 41,1±0,7a
Erythrocytes (x1012/L) 7,74±0,4 7,76±0,5 7,74±0,5 7,64±0,4 7,65±0,5
Hemoglobin (g/L) 156,1±8,7 155,4±8,7 156,2±8,1 155,3±7,9 155,8±8,4
Hematocrit (%) 43,2±0,8 42,7±0,8 42,2±0,7 43,1±0,9 42,9±0,8
Iron (pM /L) 32,4±0,9 33,4±0,7 33,7±0,8 24,2±0,9 44,6±1,2a
TIBC (pM /L) 47,6±1 48,2±0,9 48,1±0,8 44,3±1,1H 79,3±1,8Ha
UIBC (pM /L) 15,2±0,8 15,0±0,9 15,1±1 21,1±0,8 31,2±1,4Ha
TS (%) 68,6±2,6 67,1 ±2,1 68,2±2,2 55,7±2,7H 52,3±2,8Ha
Notes: ® - the result is significant in comparison with intact group, (p<0,05); a' the result is significant in comparison with previously observations term's (p<0,05).
Relatively the total iron indicators (32,4±0,9; groups accordingly, total iron indicators
32,7±1,1), TIBC (47,6±1,1;47,2±1,2), UIBC (44,9±1,6), TIBC (63,3±1,9), UIBC (20,4±1,7)
(15,2±0,3; 15,3±0,8), transferrin saturation transferrin saturation percent (71,2±2,2) of the 3r
percent (68,6±2,6; 67,9±2,2) of intact and control experimental group is significantly increases.
Table 2
Peripheral blood and iron-transport function indicators in rats - recipients 1 of experimental group after injection of animals - donors'
blood serum (n=6)
Intact Control Recipients 1 Experimental Recipients 1
Reticulocytes (%о) 18,2±0,7 17,7±0,7H 39,1±0,6H
Erythrocytes (x1012/L) 7,74±0,4 7,76±0,4 7,65±0,6
Hemoglobin (g/L) 156,1±8,7 156,2±8,5 156,4±8,6
Hematocrit (%) 43,2±0,8 43,1±0,7 42,5±0,6
Iron (pM/L) 32,4±0,9 32,7±1 44,9±1,6H
TIBC (pM /L) 47,6±1 47,2±1,2 63,3±1,9H
UIBC (pM /L) 15,2±0,8 15,3±0,8 20,4±1,7H
TS (%) 68,6±2,6 67,9±2,2 71,2±2,2H
Notes: ® - result is significant in comparison with intact group, (p<0,05).
Peripheral blood and iron transport function indicators in recipients from the 1st till 7th days do not differ from indicators of intact group (tabl. 3) that is why hereinafter these terms will not cite. Hematocrit and the reticulocytes, erythrocytes and hemoglobin quantity in recipients of experimental group during seven days remain unchanged compared control group (tabl. 3) and will not be compared further. On the first day after injection of group recipients 1 blood serum in recipients 2 of experimental group detected the increase indicators of total iron (46,7 ±0,4), TIBC (66,4±0,6), UIBC (19,7±0,7), transferrin saturation (70,7±2,8) relatively to intact group (32,4±0,9; 47,6±1; 15,2±0,8; 68,6±2,6 accordingly).
On the third day the indicators of total iron
(79,2±0,8), TIBC (110,2±0,8), UIBC (42,0±2,2), transferrin saturation (79,0±2,7) continued to increase relatively the 1s experiment day (Tab. 3) and in comparison with control rats group (31,7±0,8; 48,3±0,9; 15,3±0,9; 68,7±2,4).
On the fifth day it was determined the decrease of indicators of total iron (46,8±0,7), TIBC (67,3±0,6), UIBC (22,4±2,1), transferrin saturation (68,6±2,4) relatively the 3rd day (tabl. 3), but they increased relatively to control group (32,4±0,9; 47,3±0,7; 14,7±0,7; 67,9±2,8).
On the seventh day total iron (32,6±0,8) TIBC (48,0,2±0,6), UIBC (15,3±0,7), transferrin saturation (67,2±2,3) returned to the norm relatively to intact and control groups.
Table 3
Peripheral blood and iron-transport function indicators in rats - recipients 2 of experimental group after injection of animals -
recepients'1 blood serum (n=6)
Intact Control Recipients 2 Experimental Recipients 2
1day 3 day 5 day 7 day 1 day 3 day 5 day 7 day
Reticulocytes (%о) 18,2±0,7 18,4±0,7 18,1±0,8 17,8±0,8 18,3±0,6 18,3±0,8 19,2±0,7 18,6±0,7 18,3±0,8
Erythrocytes (X1012/L) 7,74±0,4 7,26±0,9 7,44±0,6 7,91±0,8 7,56±0,6 7,61±0,7 7,67±0,9 7,56±0,7 7,46±0,8
Hemoglobin (g/L) 156,1±8,7 158±8,8 157±9,1 1568,9 154±8,7 157,8±9,2 156,6±9,7 158,2±8,6 155,4±8,9
Hematocrit (%) 43,2±0,8 42,6±0,8 42,9±0,9 42,4±0,7 44±0,8 42,7±0,9 42,3±0,7 43,2±0,6 42,1±0,8
Iron (pM/L) 32,4±0,9 32,8±1 31,7±0,8 32,4±0,9 32,7±0,7 46,7±0,4 79,2±0,8 46,8±0,7 32,6±0,8
TIBC (pM/L) 47,6±1 48,2±0,7 48,3±0,9 47,3±0,7 48,4±0,8 66,4±0,6H 110,2±0,8Ha 67,3±0,6Ha 48,0±0,6a
UIBC (pM/L) 15,2±0,8 15,4±0,8 15,3±0,9 14,7±0,7 15,7±0,8 19,7±0,7H 42,0±2,2H 22,4±2,1Ha 15,3±0,7a
TS (%) 68,6±2,6 68,1±2,2 68,7±2,4 67,9±2,8 67,5±2,7 70,7±2,8H 79,0±2,7Ha 68,6±2,4Ha 67,2±2,3a
Notes: a- result is significant compared intact group, (p<0,05);
a- result is significant compared previously observations term, (p<0,05).
Discussion
Humans possess elegant control mechanisms to maintain iron homeostasis by coordinately regulating iron absorption, iron recycling, and mobilization of stored iron. Dietary iron absorption is regulated locally by hypoxia inducible factor (HIF) signaling and iron-regulatory proteins (IRPs) in enterocytes and systematically by hepatic hepcidin, the central iron regulatory hormone [13]. Moreover, the modeling of hypobaric hypoxia plus ferrous sulfate (FeSO4) effectively alleviated weight loss and intestinal mucosa damage induced by hypobaric hypoxia, whereas FeSO4 aggravated hypobaric hypoxia-induced weight loss, liver enlargement, spleen atrophy, and intestinal damage [12]. The iron biomarkers study in conditions of acute hypoxia after exercise showed that the level of serum ferritin and transferrin significantly were increased immediately in post-exercise conditions, but returned to baseline 3 hour later [6]. The research of a transport and metabolism adaptation under hypoxia in mountaineers determined that under hypoxemic conditions, the hepcidin function is repressed and duodenal iron transport was rapidly up - regulated. These changes may increase dietary iron uptake and allow release of stored iron to ensure a sufficient iron supply for hypoxia-induced compensatory erythropoiesis [5].
It was determined the erythropoiesis stimulation that confirmed the increase quantity of blood reticulocytes at the first day, after 18 hours staying of animals in conditions of hypoxic hypoxia. In response to said conditions, the erythropoietin was appeared in the blood, after stimulation of the erythropoiesis [3]. The indicators of transport iron in the blood serum were decreased (exception was the indicator UIBC) due to the stimulation of hematopoiesis requires more iron's quantity from the blood serum, but the increase of its absorption gets behind the needs. The absorption's increase leads to appearance in the small intestine of the new microvilli, which updated in a two days [4]. Already, at the third day after hypoxia modeling, the transport iron blood serum increasing, a reticulocytes concentration returned to normal, such as animals' blood serum with stimulated erythropoiesis obtained on the third day, after staying in a hypoxia chamber did not contain the erythropoietin (T1/2 of erythropoietin is a half of an hour) [11].
It is considered that stimulation of an iron absorption and reutilization connecting with the hepcidin' level under influence of formed during hypoxia or induced by hypoxia factor (HIF), or by stimulant erythropoiesis - erythropoietin [10]. For checking this hypothesis, we studied the influence of animals - recipient 1 serum, which was erythropoietin - free. Findings at the group of recipient 2 showed, that during erythropoiesis activating the increasing delivery of iron to the
bone marrow is not stimulated by erythropoietin. Possibly, under the action of this hormone the conditional factor of a thin humoral regulation of the iron metabolism was formed to stimulate the iron mobilization.
Conclusions and perspective
During the activation of erythropoiesis the increasing iron delivery to the bone marrow is not stimulated by erythropoietin. Researches show that under the action of this hormone the conditional factor of fine humoral regulation is formed participating in one of the stages of stimulation of iron mobilization.
Acknowledgments
The authors thank to Svetlana V. Gorbacheva from Clinical Diagnostic Laboratory of Research Educational Medical Center "University Clinic" for her assistance in conducting this study.
References
1. Воробьев А.И. Руководство по гематологии / А.И. Воробьев. -Изд. 2-е. - M. : Медицина, 2005. - 366 с.
2. Лубянова И.П. Современный обзор метаболизма железа при патологии / И.П. Лубянова // Актуальные проблемы транспортной медицины. - 2010. - № 2. - С. 47-57.
3. Павлов А.Д. Эритропоэз, эритропоэтин, железо / А.Д. Павлов, Е.Ф. Моршакова, А.Г. Румянцев. - М. : GEOTAR Media, 2011.
- 304 с.
4. Филимонов В.И. Эритропоэз и механизмы регуляции уровня железа плазмы крови / В.И. Филимонов // Газета "Новости медицины и фармации" кардиология. - 2010. - № 237.
5. Goetze O. Adaptation of iron transport and metabolism to acute high-altitude hypoxia in mountaineers / O. Goetze, J. Schmitt, K. Spliethoff [et al.] // Hepatology. - 2013. - № 58/6. - Р. 2153-2162.
- Режим доступу doi: 10.1002/hep.26581. Epub 2013 Oct 11.
6. Govus A.D. Acute hypoxic exercise does not alter post-exercise iron metabolism in moderately trained endurance athletes / A.D. Govus, C.R. Abbiss, L.A. Garvican-Lewis [et al.] // Eur. J. Appl. Physiol. - 2014. -№ 114(10). - Р. 2183-2191. - Режим доступу doi: 10.1007/s00421-014-2938-2. Epub 2014 Jul 3.
7. Muckenthaler M.U. Fine tuning of hepcidin expression by positive and negative regulators / M.U. Muckenthaler // Cell Metab. - 2008.
- № 8 (1). - Р. 1-3.
8. Roy C.N. Iron homeostasis: new tales from the crypt / C.N. Roy, C.A. Enus // Blood. - 2000. - Vol. 96, № 13. - P. 4020-4027.
9. Toledano M. Hepcidin in acute iron toxicity / M. Toledano, E. Kozer, LH. Goldstein, Abu-Kishk [et al.] // Am. J. Emerg. Med. -2009. - Vol. 27, № 7. - Р. 761-764.
10. Wei-Na Kong. Effect of erythropoietin on hepcidin, DMT1 with IRE, and hephaestin gene expression in duodenum of rats / Kong Wei-Na, Yan-Zhong Chang, Shu-Min [et al.] // Journal of Gastroenterology. - 2008. - Vol. 43, № 2. - Р. 136-143.
11. Wieczorek L. Molecular biology of Erythropoietin / L. Wieczorek, P. Hirth, K.B. Schope // Prod. Develop. Pharmac. - 1991. - № 2. -Р. 13-16.
12. Xu C. Effect of iron supplementation on the expression of hypoxia-inducible factor and antioxidant status in rats exposed to high-altitude hypoxia environment / C. Xu, C. Dong, C. Xu [et al.] // Biol. Trace Elem. Res. - 2014. - Vol. 162, № 1-3. - Р. 142 -52. - Режим доступу doi: 10.1007/s12011-014-0166-6. Epub 2014 Nov 8.
13. Zhang A.S. Molecular mechanisms of normal iron homeostasis Hematology. / A.S. Zhang, C.A. Enns // Am. Soc. Hematol. Educ. Program. - 2009. - P. 207-214. - Режим доступу doi: 10.1182/asheducation-2009.1.207.
References
1. Vorob'ev A.I. Rukovodstvo po gematologii / A.I. Vorob'ev. - Izd. 2-e. - M. : Medicina, 2005. - 366 s.
2. Lubjanova I.P. Sovremennyj obzor metabolizma zheleza pri patologii / I.P. Lubjanova // Aktual'nye problemy transportnoj mediciny. - 2010. - № 2. - S. 47-57.
3. Pavlov A.D. Jeritropojez, jeritropojetin, zhelezo / A.D. Pavlov, E.F. Morshakova, A.G. Rumjancev. - M. : GEOTAR Media, 2011. -304 s.
4. Filimonov V.I. Jeritropojez i mehanizmy reguljacii urovnja zheleza plazmy krovi / V.I. Filimonov // Gazeta "Novosti mediciny i farmacii" kardiologija. - 2010. - № 237.
5. Goetze O. Adaptation of iron transport and metabolism to acute high-altitude hypoxia in mountaineers / O. Goetze, J. Schmitt, K. Spliethoff [et al.] // Hepatology. - 2013. - № 58/6. - R. 2153-2162.
- Rezhim dostupu doi: 10.1002/hep.26581. Epub 2013 Oct 11.
6. Govus A.D. Acute hypoxic exercise does not alter post-exercise iron metabolism in moderately trained endurance athletes / A.D. Govus, C.R. Abbiss, L.A. Garvican-Lewis [et al.] // Eur. J. Appl. Physiol. - 2014. -№ 114(10). - R. 2183-2191. - Rezhim dostupu doi: 10.1007/s00421-014-2938-2. Epub 2014 Jul 3.
7. Muckenthaler M.U. Fine tuning of hepcidin expression by positive and negative regulators / M.U. Muckenthaler // Cell Metab. - 2008.
- № 8 (1). - R. 1-3.
8. Roy C.N. Iron homeostasis: new tales from the crypt / C.N. Roy, C.A. Enus // Blood. - 2000. - Vol. 96, № 13. - P. 4020-4027.
9. Toledano M. Hepcidin in acute iron toxicity / M. Toledano, E. Kozer, LH. Goldstein, Abu-Kishk [et al.] // Am. J. Emerg. Med. -2009. - Vol. 27, № 7. - R. 761-764.
10. Wei-Na Kong. Effect of erythropoietin on hepcidin, DMT1 with IRE, and hephaestin gene expression in duodenum of rats / Kong Wei-Na, Yan-Zhong Chang, Shu-Min [et al.] // Journal of Gastroenterology. - 2008. - Vol. 43, № 2. - R. 136-143.
11. Wieczorek L. Molecular biology of Erythropoietin / L. Wieczorek, P. Hirth, K.B. Schope // Prod. Develop. Pharmac. - 1991. - № 2. -R. 13-16.
12. Xu C. Effect of iron supplementation on the expression of hypoxia-inducible factor and antioxidant status in rats exposed to high-altitude hypoxia environment / C. Xu, C. Dong, C. Xu [et al.] // Biol. Trace Elem. Res. - 2014. - Vol. 162, № 1-3. - R. 142 -52. -Rezhim dostupu doi: 10.1007/s12011-014-0166-6. Epub 2014 Nov 8.
13. Zhang A.S. Molecular mechanisms of normal iron homeostasis Hematology. / A.S. Zhang, C.A. Enns // Am. Soc. Hematol. Educ. Program. - 2009. - P. 207-214. - Rezhim dostupu doi: 10.1182/asheducation-2009.1.207.
Реферат
ОСОБЛИВОСТІ ГУМОРАЛЬНОЇ РЕГУЛЯЦІЇ МЕХАНІЗМІВ ДОСТАВКИ ЗАЛІЗА ДО КІСТКОВОГО МОЗКУ ЗА УМОВ ДІЇ ГІПОКСИЧНОЇ ГІПОКСІЇ Філімонов В.І., Бурега І.Ю.
Ключові слова: еритроцит, ретикулоцит, залізо, гіпоксія, щури.
Метою роботи стало вивчення особливостей гуморальної регуляції механізмів доставки заліза в кістковий мозок в умовах дії гіпоксічної гіпоксії. Під час активації еритропоезу збільшення доставки заліза в кістковий мозок не стимулюється еритропоетином. Дослідження показали, що під дією цього гормону утворюється якийсь умовний фактор тонкої гуморальної регуляції, який впливає на метаболізм заліза, збільшуючи його рівень в сироватці крові.
Реферат
ОСОБЕННОСТИ ГУМОРАЛЬНОЙ РЕГУЛЯЦИИ МЕХАНИЗМОВ ДОСТАВКИ ЖЕЛЕЗА В КОСТНЫЙ МОЗГ В УСЛОВИЯХ ДЕЙСТВИЯ ГИПОКСИЧЕСКОЙ ГИПОКСИИ Филимонов В.И., Бурега И.Ю.
Ключевые слова: эритроцит, ретикулоцит, железо, гипоксия, крысы.
Целью работы явилось изучение особенностей гуморальной регуляции механизмов доставки железа в костный мозг в условиях действия гипоксической гипоксии. Во время активации эритропоэза увеличение доставки железа в костный мозг не стимулируется эритропоэтином. Исследования показали, что под действием этого гормона образуется некий условный фактор тонкой гуморальной регуляции, который влияет на метаболизм железа, увеличивая его уровень в сыворотке крови.
УДК 616.833.58-001.3: 615.916:546.49]-085:57.012.14: 57.084 Шамало С.М.
УЛЬТРАСТРУКТУРНІ ЗМІНИ ТРАВМОВАНОГО СІДНИЧНОГО НЕРВА ЩУРІВ НА ТЛІ РТУТНОЇ ІНТОКСИКАЦІЇ ТА ЇЇ ФАРМАКОЛОГІЧНОЇ КОРЕКЦІЇ
Національний медичний університет імені О.О. Богомольця (м. Київ)
Нагальним залишається вивчення впливу фармакологічних препаратів які б покращили механізми регенерації периферійних нервів з урахуванням трофічних факторів. Метою даного дослідження було проведення порівняльного ультраструктурного аналізу периферійного нерва щурів за умов мікромер-куріалізму із застосуванням антиоксидантного препарату та без фармакотерапії. В дослідах на білих щурах, які були розподілені на дві групи, відтворили експериментальну модель травми сідничного нерва за умов мікромеркуріалізму. У післяопераційному періоді щурам першої групи фармакотерапію не проводили, в другій групі тваринам внутрішньоочеревинно вводили щоденно протягом 2 тижнів розчин тіотриазоліну. Досліджували ультраструктурну організацію та морфометричну характеристику дистального відрізку сідничного нерва через 6 та 12 тижнів після пошкодження. Проведене дослідження свідчить, що у групи тварин, яким проводили фармакологічну корекцію тіотриазо-ліном, активується процес регенерації нерва за умов його пошкодження. Ключові слова: мікромеркуріалізм, сідничний нерв, регенерація, тіотриазолін.
Робота є фрагментом планово-дослідної роботи кафедри гістології та ембріології «Органи нервової, імунної та сечостатевої систем в умовах експериментального пошкодження» № держ. реєстрації 0112U001413
ВстуП часто перевищують гігієнічний норматив [1, 2].
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