Abstract:Inorganic nitrate supplementation is a possible therapeutic agent in diabetes. The aim of this study was to evaluate the effect of nitrate on the reproductive system in streptozotocin-induced diabetic male rats. Fifty male Wistar rats were allocated randomly to five groups: control (C), control plus nitrate (CN), diabetic (D), diabetic plus insulin (DI) and diabetic plus nitrate (DN). Sodium nitrate was administered for 2 months in the drinking water (100 mg l ) of the CN and DN groups. Insulin was injected at… Show more
“…Overall, the final body weights were significantly lower in the NO 3 supplemented groups compared to controls (WMD= -16.8 g, 95 % CI= -27.38, -6.24; P =0.002) (Figure 2 (Fig. 2) ; References in Figure 2: Ashmore et al, 2015[ 2 ]; El-Wakf et al, 2009[ 6 ], 2015[ 7 ]; Gheibi et al, 2018[ 10 ]; Hezel et al, 2016[ 13 ]; Khalifi et al, 2015[ 21 ]; Khorasani et al, 2019[ 22 ]; Norouzirad et al, 2019[ 31 ]; Oghbaei et al, 2018[ 32 ]; Roberts et al, 2015[ 35 ]; Zaki et al, 2004[ 40 ]); after exclusion of 10 experiments within the arms corresponding to high doses of NO 3 (620 and 401 mg L -1 d -1 ), overall mean differences in body weights between the groups decreased by approximately 37 % but remained statistically significant (WMD= -10.1 gr, 95 % CI= -19.0, -1.19, P =0.026).…”
Section: Resultsmentioning
confidence: 99%
“…Limited animal studies have investigated the anti-obesity effects of inorganic NO 3 as a primary hypothesis (Roberts et al, 2015[ 35 ]), while the majority of the available experiments have only reported data on body weight in NO 3 -treated animals as a secondary crude observation without any significant interpretations. This issue remains even more uncertain since inconsistent results including, higher (Hezel et al, 2016[ 13 ]; Oghbaei et al, 2018[ 32 ]), lower (Zaki et al, 2004[ 40 ]; El-Wakf et al, 2009[ 6 ]; Gheibi et al, 2018[ 10 ]; Khorasani et al, 2019[ 22 ]) or equal (Ashmore et al, 2015[ 2 ]; Khalifi et al, 2015[ 21 ]; Roberts et al, 2015[ 35 ]) weight gain have been reported in control and NO 3 -treated rats.…”
“…Overall, the final body weights were significantly lower in the NO 3 supplemented groups compared to controls (WMD= -16.8 g, 95 % CI= -27.38, -6.24; P =0.002) (Figure 2 (Fig. 2) ; References in Figure 2: Ashmore et al, 2015[ 2 ]; El-Wakf et al, 2009[ 6 ], 2015[ 7 ]; Gheibi et al, 2018[ 10 ]; Hezel et al, 2016[ 13 ]; Khalifi et al, 2015[ 21 ]; Khorasani et al, 2019[ 22 ]; Norouzirad et al, 2019[ 31 ]; Oghbaei et al, 2018[ 32 ]; Roberts et al, 2015[ 35 ]; Zaki et al, 2004[ 40 ]); after exclusion of 10 experiments within the arms corresponding to high doses of NO 3 (620 and 401 mg L -1 d -1 ), overall mean differences in body weights between the groups decreased by approximately 37 % but remained statistically significant (WMD= -10.1 gr, 95 % CI= -19.0, -1.19, P =0.026).…”
Section: Resultsmentioning
confidence: 99%
“…Limited animal studies have investigated the anti-obesity effects of inorganic NO 3 as a primary hypothesis (Roberts et al, 2015[ 35 ]), while the majority of the available experiments have only reported data on body weight in NO 3 -treated animals as a secondary crude observation without any significant interpretations. This issue remains even more uncertain since inconsistent results including, higher (Hezel et al, 2016[ 13 ]; Oghbaei et al, 2018[ 32 ]), lower (Zaki et al, 2004[ 40 ]; El-Wakf et al, 2009[ 6 ]; Gheibi et al, 2018[ 10 ]; Khorasani et al, 2019[ 22 ]) or equal (Ashmore et al, 2015[ 2 ]; Khalifi et al, 2015[ 21 ]; Roberts et al, 2015[ 35 ]) weight gain have been reported in control and NO 3 -treated rats.…”
“…For example 4, thus sections 4, 17, 30, 43, … were selected for stereological analysis. Finally, ten 5-µm sections per mice were analysed for histological study and 20-25 sections were analysed for stereological studies spermatogonia) indices (Oghbaei et al, 2018) were calculated in each animal as previously described.…”
Section: Histological and Stereological Analysis Of Testismentioning
The purpose of the research was to investigate the therapeutic ability of selenium nanoparticles (Se‐NPs) on the aflatoxin B1 (AFB1) toxicity induced in the male reproductive system. For this experiment, the mature male mice were put into four groups. Control (0.5 ml PBS, 60 days; IP, n = 7), Se‐NPs (0.5 µg kg−1 day−1 for 60 days; IP), AFB1 (4.5 mg kg−1 day−1 for 60 days; IP) and AFB1 + Se‐NPs (4.5 mg kg−1 day−1 + 0.5 µg kg−1 day−1 for 60 days; IP). After treatment, the histological structure of testis, serum testosterone level and sperm parameters, including concentration, motility, viability, morphology and DNA fragmentation, were examined. The results demonstrated that the AFB1 destroyed the testicular tissue structure and decreased the sperm concentration, motility, viability and normal morphology significantly. AFB1 also could significantly increase sperm DNA fragmentation and reduce in vitro fertilisation and embryo development compared to the control group (p < .001). Our data show that Se‐NPs could inhibit AFB1‐induced damage to the testis and improve sperm parameters as well as in vitro fertilisation and embryo production in AFB1 exposed male mice. This study revealed that the administration of Se‐NPs could attenuate the testicular injury of AFB1 and improve the male reproductive system function in AFB1 exposed mice.
“…On this basis, we followed the previous protocol that lasts over a period of 32 ± 1 days 20 . Rats received 1 mg OVA (Sigma‐Aldrich) via an intraperitoneal route on days 1 and 8.…”
Section: Methodsmentioning
confidence: 99%
“…Finally, cells were re‐suspended in low‐content glucose Dulbecco's modified Eagle's medium (DMEM/LG; Biosera) containing 10% FBS and 1% Pen ‐Strep solution (Biosera). Cells were sub‐cultured after reaching 70% to 80% confluence 20 . Passages 3 to 6 were used in the current experiment.…”
The emergence of an inflammatory condition such as asthma could affect the therapeutic potential of stem cells. Synopsis of previous documents yielded controversial outcomes, leading to a limitation of stem cell‐based therapy in the clinical setting. This study aimed to assess the impact of asthmatic serum on the MSCs aging and dynamic growth in vitro. Rats were divided into control and asthmatic groups randomly. The asthmatic change was induced using OVA sensitization. The asthmatic structural changes are monitored by conventional Haematoxylin‐Eosin staining. Thereafter, blood samples were taken and sera provided from each group. In this study, primary bone marrow mesenchymal stem cells were cultured in culture medium supplemented with normal and asthmatic serum for 7 days. The MSCs viability was examined using the MTT assay. The expression of the aging‐related gene (β‐galactosidase), and stemness‐related markers such as Sox2, Kfl‐4 and p16INK4a were analysed by real‐time PCR assay. Histological examination revealed chronic inflammatory remodelling which is identical to asthmatic changes. MTT assay showed a reduction of mesenchymal stem cell viability compared to the control group (P < .05). Real‐time PCR analysis revealed a down‐regulation of stemness‐related markers Sox2, Kfl‐4 and p16INK4a coincided with aging changes (β‐galactosidase) compared to the control group (P < .05). These data show the detrimental effect of asthmatic condition on bone marrow regenerative potential by accelerating early‐stage aging in different stem cells and further progenitor cell depletion.
Significance of the study
In such inflammatory conditions as asthma, the therapeutic potential of stem cells may be altered. We demonstrate that serum from asthmatic rats had the potential to reduce the viability of mesenchymal stem cells in vitro. Furthermore, we observed that the expression of the aging‐related gene known β‐galactosidase was statistically increased in cells co‐cultured with asthmatic serum. At the same time, expression of stemness‐related markers Sox2, Kfl‐4 and p16INK4a down‐regulated. These results support the damaging effect of asthmatic condition on bone marrow regenerative ability by inducing early‐stage aging in stem cells and additional progenitor cell reduction.
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