Journal List > J Severance Union Med Coll > v.2(1) > 1093711

CHOI: The Effect of Hormones on the Sedimentation Velocity of Red Blood Cells after Blockade of the Reticulo-endothelial System.

CONTENTS

1. Introduction.
2. Experimental Materials and Method.
3. Results.
1) Control.
a. The effect of normal saline injection.
b. The effect of withdrawal of blood for experiment.
2) The effect of hormones on the sedimentation velocity of red blood cells after blockode.
a. The effect of thyroid hormone.
1. Effect of thyroidectomy in normal rabbits.
2. Effect of thyroidectomy after blockade
3. Effect of thyroid medication in normal rabbits.
4. Effect of thyroid medication after blockade.
b. The effect of parathyroid hormone.
1. Effect of parathyroidectomy in normal rabbits.
2. Effect of parathyroidectomy after blockade.
3. Effect of injection of parathormon in normal rabbits.
4. Effect of injection of parathormon after blockade.
c. The effect of spleen hormone.
1. Effect of splenectomy in normal rabbits.
2. Effect of the splenectomy after blockede.
3. Effect of injection of spleen emulsion into normal robbits.
4. Effect of injection of spleen emulsion after blockade.
d. The effect of adrenal hormone.
1. Effect of cortex hormone.
A. Effect of cortex hormone in normal rabbits.
B. Effect of cortex hormone after blockade.
2. Effect of adrenalin.
A. Effect of adrenalin in normal rabbits.
B. Effect of adrenalin after blockade.
e. The effect of insulin.
1. Effect of insulin in normal rabbits.
2. Effect of insulin after blockade.
f. The effect of the sex hormone.
1. Effect of the testicular hormone.
A. Effect of orchidectomy in normal rabbits.
B. Effect of orchidectomy after blockade.
C. Effect of injection of testicular hormone into normal rabbits.
D. Effect of injection of testicular hormone after blockade.
2. Effect of ovarian hormone.
A. Effect of ovariectomy in normal rabbits.
B. Effect of ovariectomy after blockade.
C. Effect of injection of ovarian hormone into normal rabbits.
D. Effect of injection of ovarian hormone after blockade.
3) The influence of certain physico-chemical changes of the blood on sedimentation velocity after blockade of the reticulo-endothelial system.
1. Blood cells and hemoglobin.
2. Blood volume, viscosity and fragility of the red blood cells.
3. Globulin, albumin and fibrinogen content of the blood.
4. Blood calcium, blood cholesterol and blood sugar.
4. Discussion.
5. Summary.
Bibliography.

1. INTRODUCTION

It is well known that changes in the red cells occur when certain influences act upon the living organism. Since Fahraeus (21) reported in 1918 that the rate of sedimentation in pregnant woman is greater than in the normal woman, many investigators have reported on the subject. Many of these experimental reports had a direct clinical value. Such papers are those of Okada (92), Kanemori (52), Shibayama (110), Otani (86), Takebayashi (111), Hayashi (30), Okamura (93), Klinck (150), Gram (23), Schafer (106), and Kagan (149).
On the other hand, other writers insisted that the cause of the phenomenon was to be found in the serum, for example Pines and Jaffe (151), Knosp (44), Ryan, Johnson and Gesishimer (97), Pico Franceshi and Negrete (20), Klinck (150), Minamiyoshi (73), Hayashi (30), Shimizu (101), Yo (135), Yoshida (136), Jindo (145).
But as a matter of fact the causative factor is still unknown. Recently in my studies on the function of the reticulo-endothelial system by such investigators as Uno (123), Kiyono (49), Matsuhara (80), Klinck (150), a new factor has suggested itself and in the light of most recent knowledge we wish to report on the relationship between the sedimentation velocity of the red cells and the various body hormones.

2. EXPERIMENTAL MATERIALS AND METHOD

Normal male rabbits weighing about 2 kg. were used through out this experimental work, except when female rabbits were necessary. Westergrens apparatus was used for measurement of the sedimentation velocity. The sample of blood was drawn from the neck vein of the fasting animal and 10% of Indian ink in saline was used for blockading the reticulo-endothelial system (R. E. S.).

3. RESULTS

1) CONTROL

A) THE EFFECT OF NORMAL SALINE SOLUTION INJECTION

The India ink was diluted with normal saline solution and injected to note its intrinsic effect. The influence on sedimentation velocity (S.V.) of red blood cells after the injection of saline solution has been noted by many investigators. However Otani (86), Hotachi (35) found no change on the S. V. after saline injection while Ishiwari (41) observed that the injection of large doses of saline solution accelerate the S. V. of red cells.
The normal saline was injected daily for six days (5 cc per K. G. body weight intravenously once a day), [Table 1 and 2].
Thus no effect of the S. V. of red cells was noted after the injection of normal saline solution.

B) THE EFFECT OF WITHRAWAL OF BLOOD FOR EXPERIMENT.

Variation of the S. V. of red cells during manipulation has been proved by many investigators. Thus Miwa(67) found the accelerated speed of S. V. of red cells in the artery when compared with the vein.
Otani (95) found increased velocity of sedimentation rate when blood was withrawn, while Araki (1) and Hotacni (35) noted no effect on the S. V. of red cells after withrawal of blood several times with 4 to 7 days. Takashina (112) found increased rate of sedimentation when about 7 cc blood was withrawn daily, and Takebayashi (111), Shibayama (110), Okamura (93) also found a relationship between the S. V. of red cells and quantity of blood withdrawn.
Blood was withdrawn at variable intervals and results are recorded in table 3 and 4.
There are no special changes on the S. V. of red cells, after experimental venepuncture in normal rabbits as table 3 and 4 show.

2) THE EFFECT OF HORMONES ON THE SEDIMENTATION VELOCITY OF RED CELLS AFTER BLOCKADE.

We know that R. E. S. has an important function in the life processes as Aschoff and Kiyono have shown. It is reasonable to expect important changes in the body when the function of R. E. S. has been stimulated or inhibited. But Nagao noted that no change occured in nutrition and developement when Indian ink has been used to blockade the R. E. S. Uno (123) noted that Indian ink was absorbed by both liver and spleen. Tsunashima (115) reported the increase of S. V. after injection of colloidal silver or after splenectomy. Tsunekawa (122) and Matsuhara (80) noted an increase of S. V. when the R. E. S. was blockaded by the injection of Indian ink. Seiffert (99) noted increase of sedimentation velocity after splenectomy and blockade of the R. E. S. in the guinea pig. Klinck (150) reported that the dose does not influence the S. V. when trypan blue has been injected into normal rabbits [Table 5, 6 and 7].
The rate of S. V. was augmented by blockade of the R. E. S.

a. EFFECT OF THYROID HORMONE

Many reports have appeared on the relationship between the S. V. of red cell and function of the thyroid gland.
Thus Trifon (115) noted the increase of S. V. when a diet containing thyroid substance was given while Bonilla and Moya (12) studied S. V. before and after thyroidectomy. Westergren (129) believes that the thyroid exerts a definite influence upon the S. V. of erythrocytes. Vasaturo (134) has investigated the sedimentation time in thyroidectomized, thyro-para- thyroidectomized animals and Wakata(130) has noted that the sedimentation velocity was accelerated by thyro-thymo-orchidectomy for at least 40 days. Tsunashima (155) reported that the S. V. of red cells decreased by thyroidectomy was later increased by administration of thyroid extract, but the rate of globulin and albumin does not stimulated. Takebayashi (111) noted no effect of S. V. of red blood cells under such conditions. Mensch (81) reported rapid S. V. in Basedow’s disease, and Sugano (107) also reported decreased volume of red cells in Basedow’s disease. Heing, Taterka, Goldmann (28) have studied rapid S. V. in Basedow’s disease. Yun (144) also studied the influence of thyroidectomy upon erythrocyte sedimentotion without any definite results.

1. EFFECT OF THYROIDECTOMY IN NORMAL RABBITS

The results are recorded in the following tables 8, 9, 10.
In my study, also there was no influence of thyroidectomy upon sedimentation of red blood cells.

2. EFFECT OF THYROIDECTOMY AFTER BLOCKADE

The results are expressed in the following tables 11, 12, 13.
Thus thyroidectomy after blockade has no definite effect upon the erythrocyte S. V.

3. EFFECT OF THYROID MEDICATION IN NORMAL RABBITS

Thyreoglandol was given at the rate of 0.5 cc per k.g. and the results are recorded in the following tables 14, 15.
The above tables show no relation.

4. EFFECT OF THYROID MEDICATION AFTER BLOCKADE

Thyreoglandol also was given after blockade and results are recorded in the following tables 16, 17.
Thus, there was no special influence on S. V. of red blood cells after thyroidectomy or thyroid medication.

b. THE EFFECT OF PARATHYROID HORMONE

Since Collip (14) succeded in isolating the parathyroid hormone many articles by many investigators have appeared and it has been clearly shown that there is a relationship between calcium metabolism and this substances.
Bomsker (11) reported that two different action on the blood calcium, Oshima (91) also reported on the subject. Zimmerman (143) noted absence of any effect on the calcium and coagulation time even after parathormone was injected. Bonilla and Moya (12) and Vasaturo (134) noted increased S. V. of red cells after parathyroidectomy, but Vasaturo (134) noted decreased S. V. of red cells after thyroparathyroidectomy. Yun(144) reported increased S. V. of red cells after parathyroidectomy.

1. EFFECT OF PARATHYROIDECTOMY IN NORMAL RABBITS

Both parathyroid gland 2 out of 4 were removed from normal rabbits, and the results are recorded in the following tables 18, 19, 20.
As shown in above tables, the S. V. of red cells was increased.

2. EFFECT OF PARATHYROIDECTOMY AFTER BLOCKADE

The results are shown in the following tables 21, 22.
The rate of sedimentation was increased.

3. EFFECT OF INJECTION OF PARATHORMONE IN NORMAL RABBITS

Parathormone was given intravenously at the rate of 1 to 5 units per k.g. and the results are noted in the following tables 23, 24, 25.
There was no special effect on the sedimentation velocity of red blood cells after the injection of parathormone.

4. EFFECT OF INJECTION OF PARATHORMONE AFTER BDOCKADE

Parathormone was given as in number 3 and the results are noted in the following tables 26, 27.
I found that there were no effect of parathormone injection on the red cell sedimentation after blockade.

c. THE EFFECT OF SPLEEN HORMONE

The spleen has only recently been recognized as an organ of internal secretion. The relationship betweeu[n] the S. V. of erythrocytes and spleen function has been reported by many investigators. Kosawa reported increased fibrinogen content of the blood after splenectomy. Kame (154) noted increased globulin and decreased albumin in blood after splenectomy. Takashima (112) and Kitaoka (60) have reported on the blood coagulation time. Sakai (105), Shibayama (110), Tsunashima (155), Matsuhara (80), Seiffert (99) reported rapid sedimentation rate of erythrocytes after splenectomy, while no effect upon the S. V. of red cells was noted after splenectomy.

1. EFFECT OF SPLENECTOMY IN NORMAL RABBITS

The results are recorded in the following tables 28, 29.
I found a rather more rapid sedimentation rate after splenectomy in normal rabbits.

2. EFFECT OF SPLENECTOMY AFTER BLOCKADE

The results are shown in the following tables 30, 31.
As the tables show the S. V. of erythrocytes was augmented.

3. EFFECT OF THE INJECTION OF SPLEEN EMULSION INTO NORMAL RABBITS

2% spleen emulsion was injected intravenously at the rate of 1.0 cc per k.g. The results are recorded in the following tables 32, 33.
There are no special changes in the S. V. of red cells after the injection of spleen emulsion in normal rabbits.

4. EFFECT OF THE INJECTION OF SPLEEN EMULSION AFTER BLOCKADE.

The results are recorded in the following tables 34, 35.
The injection of spleen emulsion after blockade showed no special effect.

d. THE EFFECT OF ADRENAL HORMONE

Since Addison reported in 1855 the syndrome known as Addison’s disease, and Takamine succeeded in 1901 in isolating adrenalin, many investigators have reported on this subject. The relationship between the S. V. of red cells and adrenalin gland hormones have been investigated by such workers as Seuderi, Morros, Sarda and Gaston who studied the sedimentation time in epilepsy, and Takebayashi (111) Ishiwari (41), Okamura (93) who studied the rapid sedimentation of erythrocytes after injection of adrenalin. Watanabe (131132) however reported no influence upon the sedimentation time.

1. EFFECT OF CORTEX HORMONE

Interenin by intravenous injection, was used at the rate of 1 cc per k.g. of body weight.

A. EFFECT OF CORTEX HORMONE IN NORMAL RABBITS

My results are given in the following tables 36, 37.
In the rabbits receiving interenin intravenously, augmentation of the velocity was noted.

B. EFFECT OF CORTEX HORMONE AFTER BLOCKADE

The results are recorded in the following tables 38, 39.
There is no influence upon the sedimentation time due to interenin injection.

2. EFFECT OF ADRENALIN

1: 1000 adrenalin solution (Sankyo) was injected intravenously at the rate of 0.5 cc per k.g. of body weight.

A. EFFECT OF ADRENALIN IN NORMAL RABBITS

The following tables 40, 41 show the results.
The S. V. of red cells is decreased, but not markedly.

B. EFFECT OF ADRENALIN AFTER BLOCKADE

The following tables 42, 43 show my realts [results].
The S. V. of red cells is increased after the injection of Indian ink, but is decreased after the injection of adrenalin.

e. THE EFFECT OF INSULIN

Since Banting discovered insulin in 1923, many investigations have been reported on the subject, especially on the relatiohship between insulin and blood sugar. Kanemori (52) repored decreased S. V. of red cells during convulsions due to insulin. Jindo (145) reported decrease after removal of the pancreas and increase after the injection of insulin. Pico- Francesche and Negrete (20) reported both increase of S. V. of red cells and lower blood sugar. Martens (79) recorded a relation betwren S. V. of red cells and necrosis of the pancreas.

1. EFFECT OF INSULIN IN NORMAL RABBITS

Insulin (Lilly) was used at the rate of 1-5 units per k.g. and the resulis are recorded in the following tables 44, 45.
As the tables show, the velocity was decreased but not markedly.

2. EFFECT OF INSULIN AFTER BLOCKADE

Insulin was given at the rate of 1-5 units per k.g. after blockade and the results are recorded in the following tables 46, 47.
As shown in the tables the velocity first decreased but later increased.

f. THE EFFECT OF SEX HORMONE

Since Fahraeus (21) reported in 1918 that the velocity of sedimentation is increased in the pregnant woman as compared witn the nonpregnant woman, many investigators have reported a relation between sex and the sedimentation rate. Marukami (72), Kimura (51), Ryan and Johnson (97), Ogasahara (89), Takebayashi (111), Trifon(115) reported decrease of S.V. of red cells after ovariotomy and Ogasahara (89) reported increase of S. V. of red cells but it was uncertain as to whether the reaction is entirely due to luteohormone. Takebayashi (111) reported no special influence on the S. V. of red cells after ovariotomy, except a slight increase of S. V. of red cells for a few days. Uta (124)(129) reported no effect of ovarian hormone on the S. V. of red cells and the results are not the same when the urine of pregnant women was injected. Wakata (130) reported increase of sedimentation rate after orchidectomy but was uncertain as to whether the reaction was actually due to the operation and it was most reported by thyreo-thymectomy. Trifon (115) also reported increase of velocity after orchidectomy. Vasaturo (134) reported no definite effect on the sedimentation rate. Kanemori (52) reported increased velocity after orchidectomy but no change at all after the injection of the testicular hormone. Takebayashi (111) reported no influence of orchidectomy. Yun (144) reported increased velocity after orchidectomy.

1. EFFECT OF TESTICLE HORMONE

A. EFFECT OF ORCHIDECTOMY IN NORMAL RABBITS

Both testicles were removed. The results are recorded in the following tables 48, 49, 50.
As the tables show, the velocity was increased after castration.

B. EFFECT OF ORCHIDECTOMY AFTER BLOCKADE

Both testicles were removed after blockade, and the results are recorded in the following tables 51, 52, 53.
As shown in the tables, the velocity is also increased by castration.

C. EFFECT OF INJECTION OF TESTICLE HORMONE INTO NORMAL RABBITS

The testiglandol was injected intravenously at the rate of 1 cc per k.g. and the results are shown in the following tables 54, 55.
Thus, the velocity is also decreased by injection of testiglandol.

D. EFFECT OF INJECTION OF TESTICLE HORMONE AFTER BLOCKADE

The results are recordod [recorded] in the following tables 56, 57.
There was no influence due to testiglandol on the velocity after blockade.

2. EFFECT OF OVARIAN HORMONE

A. EFFECT OF OVARIOTOMY IN NORMAL RABBITS

Both ovaries were removed, and the results are shown in the following tables 58, 59.
There was no special influence of the S. V. of red cells after ovariotomy in normal rabbits.

B. EFFECT OF OVARIOTOMY AFTER BLOCKADE

Both ovaries were removed. The results are recorded in the following tables 60, 61.
The S. V. of red cells increased after blockade and ovariotomy.

C. EFFECT OF INJECTION OF OVARIAN HORMONE IN TO NORMAL RABBITS

Ovaglandol was injected at the rate of 1 cc per k.g. and the results are noted in the following tables 62, 63.
The S. V. of red cells increased after the injection of ovaglandol in normal rabbits.

D. EFFECT OF INJECTION OF OVARIAN HORMONE AFTER BLOCKADE

Ovaglandol was given as above after blockade, and the results are recarded in the following tables 64, 65.
HE S. V. of red cells decreased as a result of ovaglandol injection after blockade.

3) THE INFLUENCE OF CERTAIN PHYSICO-CHEMICAL CHANGES OF THE BLOOD ON SEDIMENTATION VELOCITY AFTER BLOCKADE OF THE R.E.S.

Numerous investigators have confirmed the main facts about S. V. of red cells. But Okada (92), Klinck (150), Kanemori (52) Shibayama (110) Otani (95), Hubbard and Geiger (33), Kagan (149), Minamiyoshi (73), Okamura (93) state that cells or hemoglobin are the main factors while Takebayashi (111), Pines and Joffe (96), Knosp (54), Ryan, Johnson, Geishimer (97) Pico-Franceschi & Negrete (20), Nakayama & Shimoi (84), Klinick (150), Takebayashi (111), Asahi (4), Tsunashima (155), Sano (108), Shimizu (101), Yo (135), Linzenmeir (62), Uebara (124), Murakami (72), state that some constituent of serum is the primary factor. Evidently they do not agree themselves, and a final satisfactory explanation has not been reached as yet.

1. BLOOD CELLS AND HEMOGLOBIN

The Thomas-Zeiss’ method and Sahli’s method were used. The following table gives my results [Table 66].
As shown in the table in every case the white cell count inceeased and the red cell and hemoglobin decreased after blockade.

2. BLOOD VOLUME, VISCOSITY AND FRAGILITY OF ERYTHROCYTES

Hedin-Koeppe’s method and Hess' Viscosimeter were used and
0. 58%-0.32% of salt solution used for testing fragility of the erythrocytes, and the series of saline solutions varied 0.02%. The results are recorded in the following table 67.
The results recorded, show that the blood volume decreased after blockade and there was no positive effect on the sedimentation velocity. There was also no noticiable effect on the fragility of the rod blood cells after blockade.

3. GLOBULIN, ALBUMIN AND FIBRINOGEN CONTENT OF THE SERUM

Abbes refraktometer was used for this work. The results are recorded in the following table 68.
As shown by the table, the globulin, albumin and content show no special relation with the S. V. of red cells, and fibrinogen content was increased in them after blockade.

4. BLOOD CALCIUM, BLOOD CHOLESTEROL AND BLOOD SUGAR CONTENT

Kramer-Tisdal’s method for calcium and Sachett’s modification of Bloor’s method for cholesterol, Hagedorn and Jensen’s method for sugar were used. The results are recorded in the following table 69.
As the table shows the serum calcium increased after blockade and the blood sugar also increased. There was no definite change in the blood cholesterol.

DISCUSSION

In summarizing the above mentioned experiments, I found that the S. V. which depends upon certain physico-chemical changes in the blood is influenced by certain endocrine glands and by the R. E. S. When the R. E. S. is blockaded by an injection of Indian ink, the S. V. become increased.
No influence on the S. V. by thyroidectomy in normal rabbits and no influence on the S. V. after the injection of thymoglandol was noted in normal or blockaded rabbits.
After parathyroidectomy the S. V. increased in normal and blockaded rabbits, and no influence was noted on the S. V. after the injection of parathormon. The S. V. increased after splenectomy in normol or blockaded rabbits. But no influence on the S. V. was noted after the injection of spleen emulsion in either normal or blockaded rabbits. The S. V. is increased by an injection of interenin, but it is decreased (or inhibited) in blockaded rabbits.
After adrenalin injection the S. V. decreased in normal or blockaded rabbits. After insulin injection the S. V. is decreased in the normal rabbits, but in blockaded rabbits there is no definite effect.
Many reports agree that the S. V. is influenced by sex. The S. V. is increased in normal or blockaded rabbits by castration, but no influence on the S. V. is noted in normal or blockaded rabbits receiving testiglandol.
In normal rabbits the S. V. is only sligtly increased by ovariotomy, but the S. V. increased in blockaded ovariotomized rabbits and the injection of ovaglandol maintains protects the S. V. in normal or blockaked rabbits, but the effect is not marked.
Since the above changes occurred in my experimental work, as the result at the time of the removal of endocrine organs or exhibitions of endocrine substances I attemped to accertain what phpsico-chemical changes occured in blockaded rabbits. I found that red cells, hemoglobin and blood volume all decreased but white cell count increased. The viscosity was not affected. Fragility of the erythrocyte, globulin and albumin did not show any remarkable change, the blood calcium increased. Blood sugar and cholesterol are not appreciably changed, and there was the increase of fibrinogen.
Thus both blood cells and seem to have an important influence on the acceleration of S. V. of red cells after R. E. S. blockade. But it is very diffcult to say that these are the only influences at work on the S. V. of red cells. It Is also impossible to maintain that any single organ has an influence on the S. V. of red cells from the results of extirpation of endocrine organs or administration of certain endocrine substance after R. E. S. blockade in experimental animals.

CONCLUSIONS

  1. The S. V. of red cells is increased by R. E. S. blockade.

  2. The S. V. of red cells increased after parathyroidectomy, splenectomy, also after orchidectomy and ovariotomy; also after interenin injection. It is decreased after the injection ef adrenalin and insulin.

  3. The S. V. of red cells is increased by castration, splenectomy and ovariotomy after R. E. S. blockade, and is decreased by injection of interenin, adrenalin, insulin and ovaglandol after R. E. S. blockade.

  4. The Erythrocyte count, hemoglobin and blood volume is decreased when the S. V. of red cells increased as a result of R E. S. blockade, while the white cell count increased. There seems to be no definite relationship of the S. V. with globulin, albumin, cholesterol, viscosity or fragility of erythrocytes after R. E. S. blockade. However blood sugar, fibrinogen and serum calcium did increase somewhat.

The author wishes to express his thanks to Prof. I. S. Yun for his generous assistance and guidance at all times and to thank Drs: N. Found, M. S. Kim, and S. Lee for their advice.

Figures and Tables

Table. 1

1.8 kg M

jsumc-2-17-i001
Normal After injection
1 hr 2 2
2 hrs 4 3.5
3 hrs 6 5.5
Table. 2

2.0kg M

jsumc-2-17-i002
Normal After injection
1 hr 2 2
2 hrs 3.5 4
3 hrs 5 5.5
Table. 3

2.0 kg M

jsumc-2-17-i003
Normal After blood drawn
15' 30' 60' 2 hrs 4hrs
1 hr 1.5 1.5 1.5 1.5 1.5 2.0
2 hrs 3.0 3.0 3.0 3.0 3.0 3.5
3 hrs 5.0 4.5 5.0 5.0 5.0 5.5
Table. 4

1.8 kg M

jsumc-2-17-i004
Normal After blood drawn
15' 30' 60' 4hrs
1 hr 2 2 1.5 2 2
2 hrs 4 4 2.5 3 3
3 hrs 5.5 6 3.5 5 5.5
Table. 5

1.65 kg M

jsumc-2-17-i005
Normal After blockade
1 hr 2.0 2.5
2 hrs 3.0 4.0
3 hrs 4.5 6.0
Table. 6

2.0 kg M

jsumc-2-17-i006
Normal After blockade
1 hr 2.0 2.0
2 hrs 4.0 4.0
3 hrs 5.0 6.0
Table. 7

2.3 kg M

jsumc-2-17-i007
Normal After blockade
1 hr 1.5 2.0
2 hrs 3.0 4.0
3 hrs 4.5 5.0
Table. 8

2.0 kg M

jsumc-2-17-i008
Normal After thyroidectomy
2 D 4 D 10 D
1 hr 2 2 2 2
2 hrs 4 4 3 4
3 hrs 5 5.5 4 5
Table. 9

2.3 kg M

jsumc-2-17-i009
Normal After thyroidectomy
2 D 4 D 10 D
1 hr 2 2 2 2
2 hrs 4 4 4 4
3 hrs 5.5 5 6 6
Table. 10

1.6 kg F

jsumc-2-17-i010
Normal After thyroidectomy
5 D 10 D
1 hr 2 2 2
2 hrs 3.5 4 4
3 hrs 5 5 6
Table. 11

2.0 kg M

jsumc-2-17-i011
Normal Blockade and thyroidectomy
1 hr 2 2.5
2 hrs 4 4.5
3 hrs 6 6.5
Table. 12

2.0 kg M

jsumc-2-17-i012
Normal Blockade and thyroidectomy
1 hr 2 2
2 hrs 4 4
3 hrs 5 6
Table. 13

2.0 kg M

jsumc-2-17-i013
Normal Blockade and thyroidectomy
1 hr 2 2
2 hrs 3.5 4
3 hrs 5 5.5
Table. 14

2.0 kg M

jsumc-2-17-i014
Normal After injection
15' 30' 60' 2h 4h 24h
1 hr 1.5 2 2 1.5 2 2 2
2 hrs 3 3.5 3 2.5 3 3 4
3 hrs 4 4.5 4 3.5 4 5 5
Table. 15

2.0 kg M

jsumc-2-17-i015
Normal After injection
15' 30' 60' 2h 4h 24h
1 hr 2 2 1.5 2 2 2 2
2 hrs 3.5 4 3 4 4 3.5 4
3 hrs 5.5 6 5 5.5 6 5 6
Table. 16

2.0 kg M

jsumc-2-17-i016
Normal After blockade After injection
15' 30' 60' 2h 4h 24h
1 hr 2 2.5 2 2 2 2 1.5 2.5
2 hrs 4 4.5 4 4 4 4 3.5 5
3 hrs 6 6.5 5 5 6 6 5 7
Table. 17

2.0 kg M

jsumc-2-17-i017
Normal After blockade After injection
15' 30' 60' 2h 4h 24h
1 hr 2 2.5 2 2 1.5 2 o 2
2 hrs 4 5 4 4 3.5 4 4 4
3 hrs 6 7 6 5 5.5 6 6 6
Table. 18

2.0 kg M

jsumc-2-17-i018
Normal After parathyroidectomy
4 D 10 D
1 hr 2 2 2
2 hrs 4 4 4
3 hrs 6 6 6
Table. 19

1.8 kg M

jsumc-2-17-i019
Normal After parathyroidectomy
4 D 10 D
1 hr 2 2 2
2 hrs 4 4 4
3 hrs 5.5 6 6
Table. 20

1.8 kg M

jsumc-2-17-i020
Normal After parathyroidectomy
2 D 4 D 6 D
1 hr 2 2 2 2
2 hrs 4 4 4 4
3 hrs 5.5 6 6 6
Table. 21

2.0 kg M

jsumc-2-17-i021
Normal Blockade and parathyroidectomy
1 hr 2 2.5
2 hrs 4 4.5
3 hrs 6 6.5
Table. 22

1.8 kg M

jsumc-2-17-i022
Normal Blockade and parathyroidectomy
1 hr 2 2.5
2 hrs 4 5
3 hrs 6 7
Table. 23

2.0 kg M (5u p. k.)

jsumc-2-17-i023
Normal After injection
15' 30' 60' 2 h 4 h 24h
1 hr 2 2.5 2 2 2 2 2
2 hrs 4 4.5 4 4 4 3.5 4
3 hcs 6 6.5 6 5 5.5 4.5 6
Table. 24

1.8 kg M (lu p. k.)

jsumc-2-17-i024
Normal After injection
15' 30' 60' 2 h 4 h 24h
1 hr 2 2 2 2 2 2 2
2 hrs 4.5 3.5 4 4 4 4 4
3 hrs 6 5.5 6 5.5 6 6 6
Table. 25

1.7 kg M (2u p. k.)

jsumc-2-17-i025
Normal After injection
15' 30' 60' 2 h 4 h 24h
1 hr 1.5 2 3 2 2 2 2
2 hrs 3 4 4 4 4 4 4
3 hrs 5 4.5 5.3 5 6 6 6
Table. 26

2.0 kg M (2u p. k.)

jsumc-2-17-i026
Normal After Blockade After injection
15' 30' 60' 2 h 4 h 24h
1 hr 2 2.5 2 2 2 2 2 2
2 hrs 4 4 4.5 4 4 4 4 3.5
3 hrs 5.5 6 6 6 6 6 6 5.5
Table. 27

1.8 kg M (2up.k.)

jsumc-2-17-i027
Normal After Blockade After injection
15' 30' 60' 2 h 4 h 24h
1 hr 2 2.5 2 2 2 2.5 2 3
2 hrs 4 4.5 4.5 4 4- 4.5 4 5
3 hrs 6 7 6 6 5.5 6.5 6 7
Table. 28

1.7 kg M

jsumc-2-17-i028
Normal After splenectomy
6 D 10 D
1 hr 2 2 2
2 hrs 4 4 4
3 hrs 5 5.5 6
Table. 29

2.0 kg M

jsumc-2-17-i029
Normal After splenectomy
2 D 4 D 6 D
1 hr 2 2.5 2.5 2
2 hrs 4 4.5 5 4
3 hrs 5.5 6.5 6.5 5
Table. 30

2.0 kg M

jsumc-2-17-i030
Normal Blockade and splenectomy
1 hr 2 2.5
2 hrs 4 4.5
3 hrs 5 6.5
Table. 31

1.8 kg M

jsumc-2-17-i031
Normal Blockade and splenectomy
1 hr 2 2.5
2 hrs 3.5 4
3 hrs 4.5 6
Table. 32

1.8 kg M

jsumc-2-17-i032
Normal After injection
15' 30' 60' 2 h 4 h 24h
1 hr 2 2 2 2 2 2 2.5
2 hrs 4 4 4 4 4 4 4.5
3 hrs 5.5 6 5.5 6 5 5 7.5
Table. 33

2.0 kg M

jsumc-2-17-i033
Normal After injection
15' 30' 60' 2 h 4 h 24h
1 hr 2 2.5 2 2 2 2 2.5
2 hrs 4 5 4 4 3.5 3.5 5
3 hrs 6 7 5 6 5.5 5.5 7.5
Table. 34

1.85 kg M

jsumc-2-17-i034
Normal After blockade After injection
15' 30' 60' 2 h 4 h 24h
1 hr 2 2.5 2 2 2 2 2 2
2 hrs 4 5 3.5 3.5 4 4 4.5 4
3 hrs 6 6.5 6 5.8 6 4.5 6.5 7
Table. 35

1.9 kg M

jsumc-2-17-i035
Normal After blockade After injection
15' 30' 60' 2 h 4 h 24h
1 hr 2 2.5 2 2 2 2 2.5 3
2 hrs 4 5.5 4 3.5 4 3.5 4.5 5
3 hrs 6 6.5 6 5.8 6 4.5 6.5 7
Table. 36

2.0 kg M

jsumc-2-17-i036
Normal After injection
15' 30' 60' 2 h 4b 24h
1 hr 2 3 2.5 2.5 3.5 2' 2
2 hrs 5 6 5.5 5,5 5.5 5 4.5
3 hrs 8 9 8.5 9 8 7.5 7
Table. 37

2.0 kg M

jsumc-2-17-i037
Normal After injection
15' 30' 60' 2b 4 h 24h
1 hr 2 2 2 3 3 2 2
2 hrs 4 5 6 5 5 4 4
3 hrs 6 7 7.5 6 7 6 6
Table. 38

1.95 kg M

jsumc-2-17-i038
Normal After blockade After injection
15' 30' 60' 2 h 4 h 24h
1 hr 1.5 2.5 2.5 2 2.5 2 2 2
2 hrs 3.5 4.5 5 4 4 4 4 4
3 hrs 5.5 6.5 6.5 5 6 6 6 6.5
Table. 39

1.9 kg M

jsumc-2-17-i039
Normal After blockade After injection
15' 30' 60' 2 h 4 h 24h
1 hr 2 2 2.5 2 2 2 2 2
2 hrs 4 4 4 4 4 4 4 4.5
3 hrs 5 6 6 6 6 6 6 7
Table. 40

2.0 kg M

jsumc-2-17-i040
Normal After injection
15' 30' 60' 2 h 4 h 24h
1 hr 2 2 2 2 2.5 2 2.5
2 hrs 4 3 4 4 4.5 4 4
3 hrs 6 5 5 6.5 6.5 6 6
Table. 41

2.0 kg M

jsumc-2-17-i041
Normal Afier injection
15' 30' 60' 2 h 4 h 24h
1 hr 2 2 2 2 2 2 2
2 hrs 4 3.5 3 4 4 4 4
4 hrs 6 5 5 6 6 6 6
Table. 42

1.5 kg M

jsumc-2-17-i042
Normal After blockade After injection
15' 30' 60' 2 h 4 h 24h
1 hr 2 2.5 2 1.5. 2 2 2 3
2 hrs 4 5 3.5 3 4 4 5 5
4 hrs 6 6.5 5 5 6 6 7 7
Table. 43

2.0 kg M

jsumc-2-17-i043
Normal After blockade After injection
15' 30' 60' 2 h 4 h 24h
1 hr 2 2.5 2 2 1.5 2 2 2.5
2 hrs 4 5 4 4 3.5 4.5 4 4.5
3 hrs 6 7.5 6 6 6 7 5.5 6.5
Table. 44

1.8 kg M (1u. p. k.)

jsumc-2-17-i044
Normal After injection
15' 30' 60' 2 h 4 h 24h
1 hr 2 2 2 2 2 2 2
2 hrs 3 3 3.5 3 4 3 4
3 hrs 5 4 4 4 6 4 6
Table. 45

2.5 kg (5u. p. k.)

jsumc-2-17-i045
Normal After injection
15' 30' 60' 2 h 4 h 24h
1 lir 2 2 2 2 2 2 2.5
2 hrs 4 4 4 3.5 3.5 3.5 4.5
3 hrs 5 6 5 5 4.5 5.5 6.5
Table. 46

1.8 kg M (lu.)

jsumc-2-17-i046
Normal After blockade After injection
15' 30' 60' 2 h 4 h 24h
1 hr 2 2 3 2 2.5 3 3 2
2 hrs 4 4.5 5 4 4.5 5 5 4.5
3 hrs 6 6.5 6.5 6 6 7 7 6.5
Table. 47

2.3 kg (5u. p. k)

jsumc-2-17-i047
Normal After blockade After injection
15' 30' 60' 2 h 4 h 24h
1 hr 2 2 2 2 2 2.5 2 3
2 hrs 3.7 4 4.5 5 4 5 4 5
3 hrs 5.7 6.5 6 7 6 8 6 7.5
Table. 48

2.0 kg M

jsumc-2-17-i048
Normal After Castration
5 D 15 D
1 hr 2 2 2
2 hrs 3.5 4 4
3 hrs 5 6 6
Table. 49

1.8 kg M

jsumc-2-17-i049
Normal After Castration
6 D
1 hr 2 2
2 hrs 3 4
3 hrs 4.5 5.5
Table. 50

2.0 kg M

jsumc-2-17-i050
Normal After Castration
6 D 17 D
1 hr 2 2 2
2 hrs 3.5 4 4
3 hrs 5 6 6.5
Table. 51

2.0 kg M

jsumc-2-17-i051
Normal After blockade and castration
1 hr 2 2.5
2 hrs 4 4.5
3 hrs 5 6
Table. 52

2.0 kg M

jsumc-2-17-i052
Normal After blockade and castration
1 hr 2 2.5
2 hrs 3.5 5
3 hrs 5 7
Table. 53

2.0 kg M

jsumc-2-17-i053
Normal After blockade and castration
1 hr 2 2.5
2 hrs 4 4.5
3 hrs 5 6.5
Table. 54

1.85 kg M

jsumc-2-17-i054
Normal After injection
15' 30' 60' 2 h 4 h 24 h
1 hr 2 2 2 2 2 2 2
2 hrs 4 4 3.5 4 4 4 4
3 hrs 6 5 5 5.5 5.5 6 6
Table. 55

2.2 kg M

jsumc-2-17-i055
Normal After injection
15' 30' 60' 2 h 4 h 24 h
1 hr 2 2 1.8 1.5 1.5 2 2
2 hrs 3 3 3.8 3 3 4 3
3 hrs 4.5 4 5 4 5 6 4
Table. 56

1.7 kg M

jsumc-2-17-i056
Normal After blockade After injection
15' 30' 60' 2 h 4 h 24 h
1 hr 2 2.5 2.5 2 2 2 2 3
2 hrs 4 4.5 4.5 4 4 4 4 5
3 hrs 5 6 6.5 6 6 6 6.5 7
Table. 57

1.8 kg M

jsumc-2-17-i057
Normal Afaer blockade After injection
15' 30' 60' 2 h 4 h 24 h
1 hr 2 2 2 2 2 2 2 2
2 hrs 4 5.5 4 4 4 3 4 4
3 hrs 5.5 6.5 6 6 6 5 6 6
Table. 58

1.85 kg F

jsumc-2-17-i058
Normal After ovariotomy
4 D 8 D
1 hr 2 2 2
2 hrs 3.5 3 4
3 hrs 4.5 4.5 5
Table. 59

1.9 kg F

jsumc-2-17-i059
Normal Afcer ovariotomy
4 D 8 D
1 hr 2 2 2
2 hrs 4 4 4
3 hrs 6 5.5 6
Table. 60

1.76kg F

jsumc-2-17-i060
Normal After blockade and ovariotomy
1 hr 2 2.5
2 hrs 4 5
3 hrs 6 7
Table. 61

2.0 kg F

jsumc-2-17-i061
Normal After blockade and ovariotomy
1 hr 2 2.5
2 hrs 4 4.5
3 hrs 5 5.5
Table. 62

2.2 kg F

jsumc-2-17-i062
Normal After injection
15' 30' 60' 2 h 4 h
1 hr 2.5 2 2 2 2 2
2 hrs 4.5 3.5 3.5 4 4 4
3 hrs 6.5 5.5 5.5 5 5 5
Table. 63

2.0 kg M

jsumc-2-17-i063
Normal After injection
15' 30' 60' 2 h 4 h
1 hr 2 2 2 2 2 2
2 hrs 4 4 3.5 4 3 4
4 hrs 6 5 5.5 5.5 5 6
Table. 64

2.0 kg F

jsumc-2-17-i064
Normal After blockade After injection
15' 30' 60' 2 h 4 h 24h
1 hr 2 2 2 2 2 2 2 2
2 hrs 4 4 4 4 4 3.5 3.5 4
3 hrs 5.5 6 6 6 6 5.5 5.5 6
Table. 65

1.9 kg F

jsumc-2-17-i065
Normal After blockade After injection
15' 30' 6cr 2 h 4 h 24h
1 hr 2 2 2 2 2 2 2 2
2 hrs 3.5 4 3 3 3 4 4 4
3 hrs 4 6 5.5 5 5 6 6 6
Table. 66
jsumc-2-17-i066
No. Sex. Body weight Normal After blockade
S. V. W.B.C. R.B.C. Hb% S. V. W.B.C. R.B.C. Hb%
1 M 1.5 kg. 5.0 5000 6460000 80% 5.5 6800 5860000 66%
2 M 1.7 kg. 5.0 6500 5500000 70% 6.0 7200 4200000 65%
3 M 1.8 kg. 5.0 8000 6260000 70% 6.5 9600 4250000 55%
4 M 2.0 kg. 5.0 8600 6350000 75% 7.0 9000 6030000 60%
Table. 67
jsumc-2-17-i067
No. Sex. Body weight Normal After blockade
S. V. Blood volume Viscosity Fragility of erythrocytes S. V. Blood volume Viscosity Fragility of erpthrocytes
1 M 2.0 kg. 5.0 40 1.6 0.44% 0.48% 6.0 35 1.6 0.40% 0.50%
2 M 2.0 kg. 4.5 40 1.5 0.42% 0.50% 6.0 35 1.4 0.38% 0.48%
3 M 1.7 kg. 5.0 40 1.5 0.46% 0.50% 6.5 30 1.5 0.52% 0.50%
Table. 68
jsumc-2-17-i068
No. Sex. Body weight Normal After blockade
S. V. Protein % Globulin % Albumin % Fibrinogen % S. V. Protein % Globulin % Albumin % Fibrinogen %
1 M 1.5 kg 5 5.90 44.8 52.8 0.370 5.5 6.12 45.9 54.1 0.148
2 M 2.0 kg 5 5.03 39.5 60.5 0.367 6.0 5.03 39.5 60.5 0.388
3 M 1.7 kg 4 4.59 38.5 61.5 0.224 5.0 4.59 38.5 61.5 0.244
Table. 69
jsumc-2-17-i069
No. Sex. Body weight Normal After blockade
S. V. Serum calcium Blood cholesterol Blood sugar S. V. Serum calcium Blood cholesterol Blood sugar
kg. mg.% mg.% % mg. mg.% %
1 M 1.6 4.5 12.2 195 0.232 5.0 14.3 202 0.232
2 M 1.75 4.5 13.0 215 0.240 6.0 13.6 210 0.268
3 M. 2.0 5.0 11.4 258 0.241 6.0 13.0 250 0.255

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