Авторы

  • Dilsora Shodmonova
    Senior lecturer at the Alfraganus University

DOI:

https://doi.org/10.71337/inlibrary.uz.zdtf.62766

Аннотация

Black pepper (Piper nigrum) has been extensively used in the food industry as a spice and in traditional medicine to improve digestion and appetite. It is rich in flavonoids, polyphenols, alkaloids, and tannins. Recent studies have demonstrated its antioxidant properties, anti-aging effects, and natural antibiotic characteristics. However, the mechanisms by which black pepper extract affects cellular structures, specifically membranes, remain inadequately studied. This study investigates the effects of black pepper extract on the membrane regulatory processes of rat thymocyte cells under hypoosmotic stress conditions.


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THE EFFECTS OF PIPER NIGRUM (BLACK PEPPER) EXTRACT ON

THYMOCYTE CELLS

Shodmonova Dilsora Shokirovna

Senior lecturer at the Alfraganus University

Email address: shodmonovadilsora7@gmail.com

Orcid ID: 0009-0006-2475-8133

https://doi.org/10.5281/zenodo.14540559

Abstract

Black pepper (Piper nigrum) has been extensively used in the food industry as a spice and

in traditional medicine to improve digestion and appetite. It is rich in flavonoids, polyphenols,
alkaloids, and tannins. Recent studies have demonstrated its antioxidant properties, anti-aging
effects, and natural antibiotic characteristics. However, the mechanisms by which black pepper
extract affects cellular structures, specifically membranes, remain inadequately studied. This
study investigates the effects of black pepper extract on the membrane regulatory processes of
rat thymocyte cells under hypoosmotic stress conditions.

Introduction

Piper nigrums bioactive compounds have garnered attention for their medicinal

properties, yet their cellular impact remains poorly understood. Thymocyte cells, which are
essential to the immune system, exhibit regulatory volume decrease (RVD) mechanisms to
maintain homeostasis under osmotic stress. This study aims to elucidate the impact of black
pepper extract on the RVD mechanism in thymocyte membranes, providing insights into its
potential as an immunomodulator.

Materials and Methods

The experiments were conducted using thymocyte cell suspensions. The light

transmission of the suspension was measured to assess cell volume changes. Under
hypoosmotic conditions, thymocytes initially swell and subsequently recover their volume
through the RVD process. Black pepper extract concentrations of 5.35 μg/mL, 26.75 μg/mL, and
53.5 μg/mL were tested. The hypoosmotic medium was prepared with an osmotic pressure of
147±2 mOsm/kg H2O. Thymocyte cells were incubated for 15 minutes under these conditions,
and changes in RVD were recorded.

Results

1.

Control Group:

o

In hypoosmotic conditions, the average RVD after 15 minutes was 92.8±3.9% (n=5).

2.

Black Pepper Extract Effects:

o

At a concentration of 5.35 μg/mL, the RVD was reduced to 44.7±7.5% (n=5).

o

At a concentration of 26.75 μg/mL, the RVD was further reduced to 13.4±1.8% (n=5).

o

At a concentration of 53.5 μg/mL, the RVD was significantly inhibited, reaching 8.0±3.5%

(n=5).

The results indicate a concentration-dependent inhibition of the RVD mechanism by black

pepper extract.

Discussion

Black pepper extract demonstrated a significant inhibitory effect on the RVD process in

thymocyte cells. The inhibition appears to be linked to the blocking of ion channels involved in
volume regulation. At higher concentrations, the extract effectively prevented thymocyte cells


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109

from restoring their volume under hypoosmotic stress, suggesting potential interference with
cellular ion transport systems.

These findings provide a mechanistic understanding of how black pepper extract affects

thymocyte membranes and highlight its potential role in modulating immune cell function. The
concentration-dependent inhibition suggests that black pepper’s bioactive compounds may
serve as novel tools for exploring immune system regulation.

Conclusion

The study reveals that black pepper extract significantly inhibits the RVD mechanism in

rat thymocyte cells under hypoosmotic stress, with the degree of inhibition being
concentration-dependent. This effect likely results from the blockade of ion channels essential
for cell volume regulation. The results offer a foundation for further investigations into the
immunomodulatory potential of black pepper and its bioactive components, opening new
avenues for research in immune system regulation and therapeutic development.

References:

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Haslam E. Plant Polyphenols ’ Vegetable Tannins Revisited ’ Chemistry and

Pharmacology of Natural Products. // Cambridge University Press, Cambridge, 1989, p. 165.
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Hempling H.G., Thompson S., Dupre A. Osmotic properties of human lymphocytes. // J.

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Islam M.R., Uramoto H., Okada T., Sabirov R.Z. and Okada Y. Maxianion channel and

pannexin 1 hemichannel constitute separate pathways for swelling-induced ATP release in
murine L929 fibrosarcoma cells. // Am. J. Physiol. Cell Physiol., 2012, 303: C924-C935.
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Jia M., Ren D., Nie Y., Yang X. Beneficial effects of apple peel polyphenols on vascular

endothelial dysfunction and liver injury in high choline-fed mice. // Food Funct., 2017, Vol.8,
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Kandaswami C., Middleton E. Free radical scavenging and antioxidant activity of plant

flavonoids. // Advances in Experimental Medicine and Biology, 1994, 366, 351’356.
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Kanai N., Lu R., Satriano J.A., Bao Y., Wolkoff A.W., Schuster V.L. Identification and

characterization of a prostaglandin transporter. // Science, 1995, 268: 866-869.
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Kappler J.W., Roehm N., Marrack P. T cell tolerance by clonal elimination in the thymus.

// Cell, 1987, Vol.49, P.273-280.
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Khanbabaee K., Van Ree T. Tannins: Classification and definition. // Nat. Prod. Rep., 2001,

18: 641-649.
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K.Narendra Babu, R. Hemalatha, B. Danesh Kumar. Phytochemicals, polyphenols,

prebiotic effect of Osimum sanctum, Zingiber officinale, Piper nigrum extracts. // Journal of
Herbal Medicine, September 2018, 42-51.


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110

14.

Krasilnikov O.V., Sabirov R.Z., and Okada Y. ATP hydrolysis-dependent asymmetry of the

conformation of CFTR channel pore. // J. Physiol. Sci., 2011, 61: 267-278.
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Musayeva, S. I. (2024). ADVANTAGES AND DISADVANTAGES OF INTERACTIVE METHODS

INTRODUCING THE СLT (СOMMUNIСATIVE LANGUAGE TEACHING) APPROACH. World
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Kurbannazarova R.S., Tashmukhamedov B.A., Sabirov R.Z. Osmotic water permeability

and regulatory volume decrease of rat thymocytes. // Gen. Physiol. Biophys., 2003, Vol.22,
P.221-232.

Библиографические ссылки

Haslam E. Plant Polyphenols Vegetable Tannins Revisited Chemistry and Pharmacology of Natural Products. // Cambridge University Press, Cambridge, 1989, p. 165.

Hempling H.G., Thompson S., Dupre A. Osmotic properties of human lymphocytes. // J. Cell Physiol., 1977, Vol.93, P.293-302.

Holevinsky K.O., Jow F. and Nelson D.J. Elevation in intracellular calcium activates both chloride and proton currents in human macrophages. // J. Membr. Biol., 1994, 140, 13-30.

Imomov O.N. Ozbekistonning foydali osimliklari. // Oquv-uslubiy majmua, Namangan, 2021.

Ikejima K., Qu W., Stachlewitz R.F. and Thurman R.G. Kupffer cells contain a glycine-gated chloride channel. // Am. J. Physiol., 1997, 272, G1581-G1586.

Inoue T., Jackson E.K. Strong antiproliferative effects of baicalein in cultured rat hepatic stellate cells. // European Journal of Pharmacology, 1999, 378, 129135.

Islam M.R., Uramoto H., Okada T., Sabirov R.Z. and Okada Y. Maxianion channel and pannexin 1 hemichannel constitute separate pathways for swelling-induced ATP release in murine L929 fibrosarcoma cells. // Am. J. Physiol. Cell Physiol., 2012, 303: C924-C935.

Jia M., Ren D., Nie Y., Yang X. Beneficial effects of apple peel polyphenols on vascular endothelial dysfunction and liver injury in high choline-fed mice. // Food Funct., 2017, Vol.8, №3, P. 1282-1292.

Kandaswami C., Middleton E. Free radical scavenging and antioxidant activity of plant flavonoids. // Advances in Experimental Medicine and Biology, 1994, 366, 351356.

Kanai N., Lu R., Satriano J.A., Bao Y., Wolkoff A.W., Schuster V.L. Identification and characterization of a prostaglandin transporter. // Science, 1995, 268: 866-869.

Kappler J.W., Roehm N., Marrack P. T cell tolerance by clonal elimination in the thymus. // Cell, 1987, Vol.49, P.273-280.

Khanbabaee K., Van Ree T. Tannins: Classification and definition. // Nat. Prod. Rep., 2001, 18: 641-649.

K.Narendra Babu, R. Hemalatha, B. Danesh Kumar. Phytochemicals, polyphenols, prebiotic effect of Osimum sanctum, Zingiber officinale, Piper nigrum extracts. // Journal of Herbal Medicine, September 2018, 42-51.

Krasilnikov O.V., Sabirov R.Z., and Okada Y. ATP hydrolysis-dependent asymmetry of the conformation of CFTR channel pore. // J. Physiol. Sci., 2011, 61: 267-278.

Musayeva, S. I. (2024). ADVANTAGES AND DISADVANTAGES OF INTERACTIVE METHODS INTRODUCING THE СLT (СOMMUNIСATIVE LANGUAGE TEACHING) APPROACH. World Scientific Research Journal, 32(1), 217-219.

Kurbannazarova R.S., Tashmukhamedov B.A., Sabirov R.Z. Osmotic water permeability and regulatory volume decrease of rat thymocytes. // Gen. Physiol. Biophys., 2003, Vol.22, P.221-232.