Improvement of Phaseolus vulgaris on breastfeeding in female rats

Shiva Roshankhah; Cyrus Jalili; Mohammad Reza Salahshoor

doi:10.4103/2305-0500.254648

ORIGINAL ARTICLE

Year : 2019 | Volume : 8 | Issue : 2 | Page : 70-74

Improvement of Phaseolus vulgaris on breastfeeding in female rats

Shiva Roshankhah¹, Cyrus Jalili², Mohammad Reza Salahshoor¹
¹ Department of Anatomical Sciences, Medical School, Kermanshah University of Medical Sciences, Kermanshah, Iran
² Medical Biology Research Center, Department of Anatomical Sciences, Kermanshah University of Medical Sciences, Kermanshah, Iran

Date of Submission	07-Feb-2019
Date of Decision	15-Feb-2019
Date of Acceptance	25-Feb-2019
Date of Web Publication	26-Mar-2019

Correspondence Address:
Mohammad Reza Salahshoor
Ph.D, Department of Anatomical Sciences, Medical School, Kermanshah University of Medical Sciences, Kermanshah
Iran

Source of Support: None, Conflict of Interest: None

DOI: 10.4103/2305-0500.254648

Abstract

Objective: To evaluate effect of Phaseolus vulgaris (P. vulgaris) on the breastfeeding in female rats.
Methods: This experimental study was done from May 2018 to December 2018 in the Anatomical Department of Medical School in Kermanshah University of Medical Sciences in Iran. In this study, after one-week adaptation and fertilization by male, 40 female rats within 20 days of pregnancy (on average, every mother had 10 newborns) were equally separated into four groups (animals were administrated after delivery of offspring). Group 1 was control group receiving normal saline interaperitoneally, and groups 2, 3, 4 were treatment groups receiving the dose of 20, 50, 100 mg/kg of P. vulgaris interaperitoneally respectively once a day for 60 days. The prolactin hormone was measured by radio immune assay, number and diameter of alveoli via histological and morphometrical examinations, and receptor prolactin gene expression by real-time polymerase chain reaction method.
Results: P. vulgaris significantly improved alveoli’s number and diameter, prolactin hormone and receptor prolactin expression when compared to the control group (P<0.001).
Conclusions: P. vulgaris is helpful to improve the breastfeeding parameters of rats’ mammary glands.

Keywords: Phaseolus vulgaris, Breastfeeding, Animal

How to cite this article:
Roshankhah S, Jalili C, Salahshoor MR. Improvement of Phaseolus vulgaris on breastfeeding in female rats. Asian Pac J Reprod 2019;8:70-4

How to cite this URL:
Roshankhah S, Jalili C, Salahshoor MR. Improvement of Phaseolus vulgaris on breastfeeding in female rats. Asian Pac J Reprod [serial online] 2019 [cited 2023 Mar 25];8:70-4. Available from: https://www.apjr.net/text.asp?2019/8/2/70/254648

Foundation project: This study was supported by the Research Council of Kermanshah University of Medical Sciences for the financial support (Grant No. 97564).

1. Introduction

Herbal medicine is one of the methods to raise breastfeeding. Phaseolus vulgaris (P. vulgaris) plant, with the local name of green bean, is a herbaceous annual plant grown worldwide for its edible dry seeds or unripe fruit^[1]. This vegetable has usually been used to recover gastric ulcer, liver disease, and kidney and bladder stones in the west of the Iran. Phytochemical studies of the vegetable have revealed the existence of tannin and saponin^[2]. In customary medicine, this vegetable exhibits antihyperglycemic activity^[3]. It similarly contains vitamin D, protein and starchy materials and is used to treat skin sores, like many antibiotics^[4]. The consequences of highper formance liquid chromatography displayed that the antioxidant and anti-microbial compounds of P. vulgaris contain the highest concentrations of carvacrol and fumaric acid^[5]. The foremost rudiments of diverse slices of the vegetable have shown antioxidant properties^[6].

Breast milk can avoid some illnesses in the initial year of lifetime^[7]. However, less than 60% mothers are capable to remain breastfeeding throughout lactation period, and mothers encounter early breastfeeding discontinuation in most cases^[8]. Conversely, according to the World Health Organization, two million newborn deaths occur each year in arrears to absence of breastfeeding^[9].

Mammary epithelial cells manufacture and secrete milk. Information of the molecular proceedings in mammary epithelium cells throughout lactation would provide new knowledge for breeding of dairy cattle^[10]. Several studies on gene expression in the mammary gland have been carried out, which is invasive and costly and disturbs the normal lactation process^[11].

The equal of prolactin excretion rises physiologically throughout gravidity and post-partum during lactation^[12]. Prolactin has influence on the androgens metabolism, the secretion of the mammary gland and its associated act with androgens^[13]. Drugs are often used in treatments of reducing breastfeeding. but they are not broadly used due to their side effects^[14].

Considering that no studies have been carried out on the effects of P. vulgaris on breastfeeding, we designed this study to examine the effect of P. vulgaris on breastfeeding parameters of female rats.

2. Materials and methods

2.1. Animals

The present experimental study was carried out in the Anatomy Department of the Medical School of Kermanshah University of Medical Sciences in Iran from May 2018 to December 2018. This study was done on 40 female Wistar rats (weighing 220-250 g) at Kermanshah University of Medical Sciences. After fertilization of female rats by male, within 20 days of pregnancy, every mother had 10 newborns on average. The rats were administrated after delivery of offspring. All animals were treated in accordance with guidelines of National Institute of Health for the Care and Use of Laboratory Animals approved by Research Deputy at Kermanshah University of Medical Sciences (ethic approval No. IR.KUMS.REC.1397.564; approval date: January 31, 2018) based on World Medical Association Declaration Ethic of Helsinki. The rats were maintained on a regular diet and water ad libitrum with a 12:12 h light/dark cycle at (23±2) °C by considering 1-week adaptation prior to the experiments^[15].

2.2. Extract preparation

P. vulgaris vegetable was attained from a local store (the time of picking and buying this plant was in spring and in western Iran). After confirmation by a botanist from Department of Pharmacognosy, Faculty of Pharmacy, Kermanshah University of Medical Sciences (voucher specimen NO. PMP-919), the vegetable was cleaned. The leaves were dehydrated in shadow for 7 days and ground to power. And 100 g power was added to ethanol. The solution was kept in hot water bath. Then, the solution was progressively poured on Buchner funnel filter paper and cleaned by vacuum pump. It was then moved to rotary device to change into the additional solvent. The extract was dissolved in distilled water and administered interaperitoneally (i.p.) per a kilogram of animal’s weight^[16].

2.3. Experimental protocol

A total of 40 female rats were randomly divided into 4 groups, with 10 rats in each group. Group 1 served as control group receiving normal saline (i.p. injection), and groups 2, 3, 4 were treatement groups receiving 20, 50 and 100 mg/kg of P. vulgaris i.p. for 60 days at 10:00 am, respectively^{[16],[17],[18]}.

2.4. Radio immune assay

Twenty-four hours after the last injection, the animals were anesthetized and blood was collected from their hearts. Blood was taken from the heart and preserved at 37 °C for 30 min and was centrifuged (1 000 g) for 15 min. Samples were transferred to the Eppendorf tubes, and transferred to the freezer at -20 °C Prolactin was measured by radio immune assay method. The kit used monoclonal antibodies against 2 dissimilar prolactin epitopes. Sample was enclosed with the initially monoclonal antibody in the attendance of a secondary antibody. The quantity of radioactivity was proportional to the prolactin concentration of the sample^[8].

2.5. Reverse transcription and real-time polymerase chain reaction (PCR) analysis

Real time-PCR method was used to measure expression of receptor prolactin (PRLR) gene in the mammillary gland. On the last day of treatment, the animals were sacrificed. The mammillary gland was removed, frozen in liquid nitrogen and stored in freezer at -80 °C RNA was extracted from the mammillary tissue using RNeasy mini kit (Qiagen Co.) according to the manufacturer’s instructions. DNA samples were treated by DNase set kit (Qiagen). cDNA version was synthesized from the RNA extracted by RevertAid™ First Strand cDNA Synthesis Kit (Fermentas). The expression level of the given gene was measured with glyceraldehyde-3-phosphate dehydrogenase (GAPDH) primer as endogenous control by Maxima SYBR Green/ Rox qPCR master mix (Fermentas Co.) through comparative Ct (ΔΔ Ct) technique. The sequence of primers was listed in [Table 1]^[19],[20].

Table 1: Primers in real-time PCR.

Click here to view

2.6. Histological and morphometrical examinations

The non-parenchymal tissues (fat, fascia and vessels) were removed. Mammary glands were fixed, dehydrated, embedded and dissected using Automatic Tissue Processor (Leica, Germany). The steps of this process consequently included: fixation with 10% formal saline (for 72 h), washing thoroughly under running water, dehydration by raising doses of ethanol (50%, 60%, 70%, 80%, 90% and 100%, 3 min for each step and 100% ethanol step was repeated for three times), clearing by xylene (3 times and 10 min in each), and embedment in soft paraffin (3 times and 15 min in each). At this stage, 5-μm coronal histological thin sections were cut from paraffin-embedded blocks by a Leica Microtome (Leica RM 2125, Leica Microsystems Nussloch GmbH, Germany), and 5 sections per animal were chosen. For the unification of the section selection, 4 section intervals were selected, and finally the routine protocol for hematoxylin and eosin staining was implemented. At the end of tissue processing, the stained sections were mounted by entalan glue and assessed under a Olympus BX-51T-32E01 research microscope connected to a DP12 Camera with 3.34-million pixel resolution and Olysia Bio software (Olympus Optical Co. LTD, Tokyo, Japan). For each alveolus the complete cellular area was measured. Outline of alveolus was measured subsequently taking an image with a × 40 objective. The largest and smallest axises were measured in the drawing of each alveolus in order to estimate the mean axis^[9].

2.7. Statistical analysis

The Kruskal–Wallis test was used to examine data normality and the homogeneity of variance at a significance level of 0.05. Statistical differences between groups were analysed by one-way analysis of variance (ANOVA), followed by the Toukey test. SPSS software (Statistical Package for the Social Sciences, version 16 SPSS Inc., Chicago, IL, USA) was used. P<0.05 was considered as significant.

3. Results

3.1. Hormonal study

Prolactin hormone levels were significantly enhanced in the treatment groups compared to the control group (P<0.001) [Table 2].

Table 2: Results of prolactin hormone and mRNA expression of PRLR gene in control and experimental groups (mean ± SEM).

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3.2. mRNA expression of PRLR gene in mammillary gland

Effect of P. vulgaris on the mRNA expression of PRLR gene in mammillary gland was evaluated. P. vulgaris significantly up-regulated PRLR gene expression comparted to the control group (P<0.001) [Table 2].

3.3. Mean diameter of alveolus

P. vulgaris significantly increased the diameter of alveolus in the treatment groups compared to the control group (P<0.001) [Table 3].

Table 3: Results of alveolar number and diameter in control and experimental groups (mean ± SEM).

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3.4. Alveolus number

P. vulgaris significantly improved the mean number of alveoli of the mammary glands in the treatment groups when compared to the control group (P<0.001) [Table 3].

3.5. Histological study

In control group, mammary glands demonstrated minor lobules distributed among massive volume of adipose tissue. The gland tissue treated with P. vulgaris showed growth in the dimension of lobules and volume of alveolus which were packed through alveoli. The mammary tissue of treatment groups showed increase in the lobular size with a corresponding lessening in the adipose tissue [Figure 1].

Figure 1: Effect of P. vulgaris extract on mammary gland tissue.
a) Control group: alveolus was seen (blue arrow); (b, c, d) Treatment groups with 20, 50, 100 mg/kg P. vulgaris respectively. Growth in the size of lobules (yellow arrow) and alveolar amount were seen in the treament groups. All groups were used by hematoxylin-eosin staining with magnification × 100

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4. Discussion

Herbal medicine has diverse properties on different organs^[9], such as endocrine and exocrine glands^[8]. The study examined the effect of P. vulgaris on mammary tissue. The outcomes displayed that the expression of PRLR gene was significantly improved in the P. vulgaris groups. The PRLR gene is a cytokine receptor and has been found in alveoli of the mammary glands. The PRLR determined through a gene on chromosome 7p12-17 is relateed with prolactin by a transmembrane receptor^[21]. Raised expression of PRLR increases the serum levels of prolactin and also reduces the size of interstitial lipid tissue in breast tissue^[22]. Gass et al^[23] suggested that antioxidant compounds can raise the expression of the PRLR gene. Similarly, P. vulgaris, due to antioxidants, improves the PRLR expression in the current study. Furthermore, the consequences of Gass et al^[23] are consistent with the outcomes of the contemporary study. Saponin can up-regulate PRLR and increase the volume of milk production. In view of saponin content of P. vulgaris, the improvement of PRLR expression and prolactin level in the current study was attributed to treatment with P. vulgaris and the existence of saponin in this vegetable^[1],[2]. P. vulgaris augmented the number and diameter of alveoli in the P. vulgaris groups. This proposes that P. vulgaris has positive influence on the mammary gland. The expansion of alveoli in mammary lobules is related with serum prolactin levels during breastfeeding^[24]. It appears that this increase in alveoli was moreover linked with an increase in prolactin levels, considering that P. vulgaris contains numerous antioxidants and flavonoid compounds^[3]. Flavonoids are portion of phytoestrogens^[25]. Phytoestrogens are natural compounds resulting from plants, which in fact have the similar organization as estrogen^[26]. Increase of alveoli of the lobules may be attributed to estrogen mechanisms.

The results of Jalili et al^[8] displayed that Utrica diocia, containing the flavonoids, increased the diameter and number of alveoli in the mammillary tissue, which approves the outcomes of the current research. The existing study displayed that P. vulgaris improved the amount of prolactin of the mother rats in this study. The equal of prolactin upsurges physiologically through pregnancy and postpartum, and plays diverse roles such as stabilising the secretory action of the milk production. So, aggregated prolactin levels can be linked with a rise in milk production^[27]. The effect of P. vulgaris on prolactin hormone in the current study may be due to sufficient vital nutrients and minerals provided by this plant^[28]. It similarly seems that this vegetable is rich in tanins, ascorbic acid, saponins and many antioxidants; these compounds increase the prolactin hormone via affecting on the pituitary gland^[29].

The outcomes of AL-Shemary et al^[30] showed that tannin in Ocimum gratissmum can increase the prolactin concentration which confirms the results of the present study. The results of Daniel et al^[31] displayed that Cucurbita pepolinn extract significantly increased serum prolactin levels, which emphasizes the effect of herbal medicine on prolactin levels and is consistent with the results of the present study. According to the study results of Bolzán et al^[32], which showed that antioxidants can increase the prolactin blood level, it seems that the high antioxidant property of P. vulgaris extract is another factor leading to elevated prolactin level of animals. However, further research is needed to clarify the issues and ambiguities in this regard. However, the present study provides new evidence of the role of P. vulgaris extract in improving milk production. Determining role of molecular factors and more precise mechanisms involved in this regard will require more detailed studies.

In conclusion, the current research explores the role of P. vulgaris in improving breastfeeding. Administration of P. vulgaris leads to increased PRLR gene expression, raised serum prolactin levels, and positive variations in mammary gland tissue in favor of milk production. Examining the action of the P. vulgaris extract on breastfeeding needs more additional detailed experimentations in this regard.

Conflict of interest statement

The authors declare that there is no conflict of interest.

Acknowledgments

We gratefully acknowledge the Research Council of Kermanshah University of Medical Sciences for the financial support (Grant No. 97564).

Foundation project

This study was supported by the Research Council of Kermanshah University of Medical Sciences for the financial support (Grant No. 97564).

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