SECRETION OF ENZYMES BY SALIVARY GLANDS AND ENZYME HOMEOSTASIS UNDER THE SEPARATE AND COMBINED INFLUENCE OF HIGH TEMPERATURE AND INSOLATION

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Kodirov , S. . (2025). SECRETION OF ENZYMES BY SALIVARY GLANDS AND ENZYME HOMEOSTASIS UNDER THE SEPARATE AND COMBINED INFLUENCE OF HIGH TEMPERATURE AND INSOLATION. Journal of Multidisciplinary Sciences and Innovations, 1(1), 90–95. Retrieved from https://inlibrary.uz/index.php/jmsi/article/view/82719
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Journal of Multidisciplinary Sciences and Innovations

Abstract

X


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SECRETION OF ENZYMES BY SALIVARY GLANDS AND ENZYME HOMEOSTASIS

UNDER THE SEPARATE AND COMBINED INFLUENCE OF HIGH TEMPERATURE

AND INSOLATION

Kodirov Shokir Kodirovich

Professor of Andijan state institute, Andijan

Key words:

High temperature, insolation, enzymes, homeostasis.

Tayanch so’zlar:

yuqori temperatura, izolyatsiya, fermentlar, gomeostaz.

Ключевые слова:

Высокая температура, инсоляция, ферменты, гомеостаз.

Эксперименты проведены на 150 белых нелинейных крысах-самцах, в возрасте 2,5 мес,

средней массой 150-200 г. Полученные результаты показали, что высокая температура и

инсоляция подавляют секрецию ферментов слюнных желез: амилазу и пепсиноген, а на

липазу они не влияют.
Однонаправленные изменения активности амилазы и пепсиногена в слюнных железах и в

крови при действии высокой температуры указывают на значимость слюнных желез в их

гомеостазе.

The experiments were conducted on 150 white nonlinear male rats, aged 2.5 months,

with an average weight of 150-200 g. The results showed that high temperature and insolation

suppress the secretion of salivary gland enzymes: amylase and pepsinogen, but they do not affect

lipase.

Unidirectional changes in the activity of amylase and pepsinogen in the salivary glands

and in the blood under the influence of high temperature indicate the importance of the salivary

glands in their homeostasis.

Актуальность работы.

Высокая температура и инсоляция, как климатический фактор

оказывают значительное влияние на организм. Реакция организма на действие высокой

температуры и инсоляции чрезвычайно многообразна и сложна. Под их воздействием

нарушается водно-солевой обмен, что приводит к глубоким изменениям в деятельности

сердечно-сосудистой системы, органов пищеварения и выделения, изменяются

морфологический состав и свойства крови [1, 2, 6, 7, 8, 9, 10]. Саливация в своем объеме в

большой мере зависит от гидратированности организма [3], резко понижаясь даже при

небольшой дегидратации. В этих условиях концентрация многих рекретируемых веществ

в составе слюны повышается, а их дебиты могут снижаться.
По литературным данным слюнные железы рассматривались как орган принимающий

участие в терморегуляции [1, 6] и нет работ посвященных влиянию высокой температуры

и инсоляции на ферментовыделительную деятельность слюнных желез.

Relevance of the work.

High temperature and insolation, as a climatic factor, have a

significant impact on the div. The div’s reaction to the action of high temperature and

insolation is extremely diverse and complex.


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Under their influence, water-salt metabolism is disrupted, which leads to profound

changes in the functioning of the cardiovascular system, digestive and excretory organs, and

changes in the morphological composition and properties of the blood [1, 2, 6, 7, 8, 9, 10].

Salivation in its volume largely depends on the hydration of the div [3], sharply

decreasing even with slight dehydration. Under these conditions, the concentration of many

secreted substances in the saliva increases, and their debits can decrease.

According to literary data, the salivary glands were considered as an organ

participating in thermoregulation [1, 6] and there are no works devoted to the influence of high

temperature and insolation on the enzyme-secreting activity of the salivary glands.

Purpose of the Study.

The purpose of work was to study the enzyme-secreting activity

of the salivary glands under the separate and combined influence of high temperature, insolation

and to determine the possibility of secreting some hydrolytic enzymes in saliva, secreted by other

digestive glands (stomach, pancreas, intestines).

Material and methods.

The experiments were conducted on 150 white nonlinear male

rats, aged 2.5 months, with an average weight of 150-200 g, kept under standard conditions in

the vivarium of the institute.

The study included 3 groups of animals: 1st (n=50) - intact animals not exposed to any

influences (at an ambient temperature of 20-250C, control), 2nd (n=50) - rats at an ambient

temperature of 37-400C, 3rd (n=50) - rats in the summer - June-July (at an ambient temperature

of 37-400C) during the entire duration of the experiment were exposed to insolation on the sun

platform, daily at 1200 hours of the day, for 30 minutes.

The rats were anesthetized with ether immediately before slaughter, they were killed by

decapitation, and then their blood was collected. After slaughtering the animals, their parotid,

submandibular and sublingual salivary glands were removed. The following enzymes were

determined in the homogenate of the salivary glands and in the blood serum: amylase,

pepsinogen, lipase.

Enzymatic activity was related to 1 g of gland tissue. The obtained data were compared

with the control values.

Results and discussion.

The data we obtained showed that at high ambient temperatures (Table 1) the

amylolytic activity of salivary gland homogenates and blood decreases sharply.
In the first group of rats, when they were exposed to only one elevated temperature (without

insolation), the amylolytic activity of homogenates of the submandibular and sublingual salivary

glands and blood serum was approximately 6-7 times lower than the indicators of the control

group.

And in the homogenate of the parotid salivary gland there was an even more

pronounced decrease in amylase activity (its activity was 8-9 times less than the control group).

In the second group of rats, when they were exposed to high temperature and insolation, the

amylolytic activity of homogenates of the submandibular and sublingual salivary glands

decreased approximately 2 times than when exposed to high temperature alone.

This means that the simultaneous action of two stress factors, such as high temperature

and insolation, suppresses the activity of amylase of the submandibular and sublingual salivary

glands to a greater extent. The amylolytic activity of the parotid salivary gland and blood serum


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under the combined action of high temperature and insolation remains at the same level as under

the action of high temperature alone.

Table 1

Dependence of amylolytic activity of homogenate (mg/min) of salivary glands and amylase

content in rat blood on ambient temperature (M±m)

Material under study

At a temperature

of 20-250

0

C

At a temperature 37-40

0

С

Without insolation After insolation

Homogenate

of

the

parotid salivary gland

7207,8

99,9

227,5

21,3

*

274,9

26,2

*

Homogenate

of

submandibular

and

sublingual salivary glands

7870,9

481,8

783,8

70,54

*

419,6

38,4

*, **

Blood serum

257,6±23,2

35,8±3,49

*

40,9±3,59

*

Note:

here and in tables 1; 2; 3 *

p<0.05 compared to

values ​ ​ at a temperature of 20-250C, **

P<0.05

compared to values ​ ​ at a temperature of 37-400C

without insolation

A more pronounced decrease in the amylase output is observed under the influence of

high temperature (Table 1). In the homogenate of the parotid salivary gland, the activity is

reduced by 30 times compared to the control group, in the homogenate of the submandibular and

sublingual salivary glands, its decrease was 10 times compared to the control.

With the simultaneous action of two factors - high temperature and insolation, the

amylase activity in the homogenate of the parotid salivary gland remains the same as with the

action of only high temperature, and in the homogenate of the submandibular and sublingual

glands, its activity becomes 2 times less than with the action of only high temperature.

The ambiguity of the reaction of the salivary glands in the secretion of amylase, under

the influence of high temperature and insolation, can be explained by the presence in the blood

serum and saliva of two types of amylase, intrinsic (S) and pancreatic (P) α-amylase. The ratio of

these amylases in the saliva of the parotid gland (S - 55-67%; P - 33-44%), submandibular and

sublingual salivary glands is not the same [3].


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Table 2

Dependence of lipolytic activity of homogenate (mg/min) of salivary glands, lipase content

in rat blood on ambient temperature (M±m)

Material under study

At a temperature

20-25

0

С

At a temperature 37-40

0

С

Without

insolation

After insolation

Homogenate of the parotid salivary

gland

0,40±0,10

0,60±0,10

0,40±0,10

Homogenate of submandibular and

sublingual salivary glands

0,20±0,10

0,40±0,04

0,50±0,14

Blood serum

3,80±0,32

3,10±0,31

3,20±0,30

This means that the parotid glands secrete saliva with a higher proportion of resecreted

pancreatic amylase than the saliva of the other two glands, which is confirmed by the correlation

coefficients we obtained between the amylase content in the blood and its secretion by the

salivary glands.
The correlation coefficients between the amylolytic activity of the blood and its secretion by the

parotid gland are much higher than those of the submandibular and sublingual glands.

From this it can be concluded that the decrease in amylase activity in the salivary

glands can be explained by the suppression of the secretion of this enzyme by the salivary glands

under the influence of high temperature and insolation, and is also the result of dehydration of

the div as a whole and the salivary glands in particular.

Changes in external temperature and exposure to insolation did not affect the lipolytic

activity of blood serum and salivary glands (Table 2). Under the influence of high temperature

and insolation, its flow rate remained at the level of the control group indicators.

At high external temperatures, the content of pepsinogen in the blood, as well as in the

homogenate of the salivary glands and its secretion by the salivary glands decreases (Table 3). In

this case, the decrease in the content of pepsinogen in all three salivary glands was

approximately the same, 5-6 times less than the indicators of the control group. The same results

were also obtained with and without insolation.

Table 3

Dependence of pepsinogen content in homogenate (mg/min) of salivary glands, its content

in rat blood on ambient temperature (M±m)

Material under study

At

a

tamperature

20-25

0

С

At a temperature 37-40

0

С

Without

insolation

After insolation


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Homogenate of the parotid salivary

gland

33,0±3,0

11,50±1,09

*

11,60±1,09

*

Homogenate of submandibular and

sublingual salivary glands

39,0±3,40

11,20±1,06

*

11,00±1,07

*

Blood serum

76,20±7,58

35,80±3,52

*

31,90±3,08

*

The content of pepsinogen in the blood of experimental rats exposed to high

temperatures and insolation decreased by approximately 2.8-3.5 times compared to control

values.

The main source of pepsinogen in the blood are the chief cells of the gastric glands [4]

and pepsinogen in saliva has a recretory nature, i.e. it is secreted from the blood [5].

The high dependence of the content and especially the release of pepsinogen in the

saliva on its blood level that we have established confirms its recretory origin in the saliva. The

correlation coefficients increase sharply under the influence of high temperature and insolation,

i.e. the dependence of the release of pepsinogen in the saliva on its blood level increases.

This means that stress factors such as high temperature and insolation suppress the

secretory activity of the main cells of the stomach and reduce the secretion of pepsinogen into

the blood, and this leads, accordingly, to a decrease in its secretory release from the blood as part

of saliva.

Summarizing the obtained data, it seems possible to draw the following conclusions:
1. High temperature and insolation suppress the secretion of salivary gland enzymes:

amylase and pepsinogen, but they do not affect lipase.

2. Unidirectional changes in the activity of amylase and pepsinogen in the salivary

glands and in the blood under the influence of high temperature indicate the importance of the

salivary glands in their homeostasis.

References

1. Bozhenkova M.V. Morphology of submandibular glands of white rats that died from

heatstroke // Morphological statements (supplement). – Moscow-Berlin, 2004. – № 1-2. – P. 14.

(18)

2. Vorobyeva N.F. Peculiarities of histiocytic reaction after preliminary intake of zeolites

with food during ontogenesis during overheating and xerophagy // Pathological physiol. and exp.

therapy. – 2008. № 2. – P. 23-25.

3. Korotko G.F. Secretion of the salivary glands and elements of saliva diagnostics. - M.:

Publishing House Academy of Natural Sciences, 2006. - 192 p.

4. Korotko G.F. Gastric digestion. - Krasnodar: Publishing House of OOO BK "Group B",

2007. - 256 p.

5. Korotko G.F., Kodirov Sh.K. On the bilateral autonomy of enzyme secretion by human

salivary glands // Dentistry. - 1994. - Vol. 73, No. 1. - P. 197-198. (61)


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6. Romanov V.I. Morphology of the exocrine pancreas of white rats during acute overheating

of the div // Morphological Gazette (Supplement). - Moscow-Berlin, 2004. - No. 1-2. - P. 87. 2.

7. Romanov V.I., Bozhenkova M.V. Stromal-parenchymatous relationships in the digestive

glands of white rats during acute overheating of the div // Morphological Gazette (Supplement).

- Moscow-Berlin, 2004. - No. 1-2. - P. 88.

8. Boutilier R.G. and St-Pierre J.Surviving hypoxia without really dying // Comp. Biochem.

Physiol. – 2000. – v. 126. – P. 481-490.

9. Hochachka P.W. and Lutz P.L. Mechanism, origin, and evolution of anoxia tolerance in

animals // Comp. Biochem. Physiol. – 2001. - v. 130. – P. 435-459.

10. Mora C. and Maya M.F. Effect of the rate of temperature increase of the dynamic method

on the heat tolerance of fishes // J. Therm. Biol. – 2006. – v. 31, № 4. – P. 337-341.

References

Bozhenkova M.V. Morphology of submandibular glands of white rats that died from heatstroke // Morphological statements (supplement). – Moscow-Berlin, 2004. – № 1-2. – P. 14. (18)

Vorobyeva N.F. Peculiarities of histiocytic reaction after preliminary intake of zeolites with food during ontogenesis during overheating and xerophagy // Pathological physiol. and exp. therapy. – 2008. № 2. – P. 23-25.

Korotko G.F. Secretion of the salivary glands and elements of saliva diagnostics. - M.: Publishing House Academy of Natural Sciences, 2006. - 192 p.

Korotko G.F. Gastric digestion. - Krasnodar: Publishing House of OOO BK "Group B", 2007. - 256 p.

Korotko G.F., Kodirov Sh.K. On the bilateral autonomy of enzyme secretion by human salivary glands // Dentistry. - 1994. - Vol. 73, No. 1. - P. 197-198. (61)

Romanov V.I. Morphology of the exocrine pancreas of white rats during acute overheating of the body // Morphological Gazette (Supplement). - Moscow-Berlin, 2004. - No. 1-2. - P. 87. 2.

Romanov V.I., Bozhenkova M.V. Stromal-parenchymatous relationships in the digestive glands of white rats during acute overheating of the body // Morphological Gazette (Supplement). - Moscow-Berlin, 2004. - No. 1-2. - P. 88.

Boutilier R.G. and St-Pierre J.Surviving hypoxia without really dying // Comp. Biochem. Physiol. – 2000. – v. 126. – P. 481-490.

Hochachka P.W. and Lutz P.L. Mechanism, origin, and evolution of anoxia tolerance in animals // Comp. Biochem. Physiol. – 2001. - v. 130. – P. 435-459.

Mora C. and Maya M.F. Effect of the rate of temperature increase of the dynamic method on the heat tolerance of fishes // J. Therm. Biol. – 2006. – v. 31, № 4. – P. 337-341.