382 SYNCHRONIZING ACTIVATION TIME WITH MAXIMUM MATURATION PROMOTING FACTOR AND MITOGEN-ACTIVATED PROTEIN KINASE LEVELS DOES NOT IMPROVE BOVINE INTRACYTOPLASMIC SPERM INJECTION

2007 ◽  
Vol 19 (1) ◽  
pp. 306
Author(s):  
B. J. Woodward ◽  
W. E. Maalouf ◽  
K. H. S. Campbell

The success of bovine intracytoplasmic sperm injection (ICSI) remains low because of the tightly packed sperm nucleus failing to decondense and the need for additional external activation. Maturation promoting factor (MPF) and mitogen-activated protein kinase (MAPK) assist the breakdown of the nuclear envelope. Activities are high at the early metaphase II (MII) stage but decrease with time. We assessed MPF and MAPK dynamics during the MII stage from 24 h postmaturation (hpm) onward. We then tested the hypothesis that ICSI may be more successful if the external activation is performed following sperm exposure to maximum MPF and MAPK levels. Bovine oocytes were matured in M199 with 10% FCS, 5 µg mL−1 FSH, 5 µg mL−1 LH, 1 µg mL−1 estradiol, and 50 µL mL−1 gentamycin, and cumulus cells were removed at 18 hpm. Groups of 10 MII oocytes were sampled from 24 hpm and analyzed for MPF and MAPK activities as previously described (Ye et al. 2003 Reproduction 125, 645–656). For ICSI, MII oocytes were moved to HSOF supplemented with amino acids and BSA (HSOFaa) and injected with sperm from 19 to 22 hpm. Further MII oocytes were subjected to sham or no injections at this time. Injections were performed manually using a 1480-nm diode laser (XY-clone; Hamilton-Thorne, Beverly, MA, USA) to breach the zona pellucida. Because the maximum kinase activities were reached at 28 hpm, oocytes were activated in 2 groups: at either 24 or 28 hpm, using HSOFaa containing 7% ethanol followed by culture in mSOFaa with 10 µg mL−1 cycloheximide for 6 h, and then transferred to mSOFaa medium until cleavage assessment on Day 2. Differences in the percentage of cleaved oocytes in the different groups were analyzed by a chi-squared test. From 24 to 28 hpm, there was an increase in both MPF (24.6%) and MAPK (58.7%) levels, followed by a slow decline. There were no significant differences in cleavage rates for sham-injected or control oocytes at the different activation times (P < 0.05). However, a significantly higher cleavage rate was observed following ICSI with activation at 24 hpm compared with 28 hpm (P < 0.001), even though kinase levels appeared maximal at 28 hpm. The manual injection procedure appeared detrimental, because oocytes in the control group showed a significantly higher cleavage rate than sham-injected oocytes (P < 0.01). In conclusion, bovine oocytes subjected to ICSI showed a better cleavage rate if external activation was performed at 24 hpm rather than at 28 hpm, even though the MPF and MAPK levels were maximal at 28 hpm (P < 0.001), even though kinase levels appeared maximal at 28 hpm. The manual injection procedure appeared detrimental, because oocytes in the control group showed a significantly higher cleavage rate than sham-injected oocytes (P < 0.01). In conclusion, bovine oocytes subjected to ICSI showed a better cleavage rate if external activation was performed at 24 hpm rather than at 28 hpm, even though the MPF and MAPK levels were maximal at 28 hpm. Table 1. Percentage of Day 2 cleaved oocytes after intracytoplasmic sperm injection, sham or no injection at 2 different activation times

2020 ◽  
Vol 150 (7) ◽  
pp. 1731-1737
Author(s):  
Qi Xu ◽  
Ziyu Chen ◽  
Borong Zhu ◽  
Gaorui Wang ◽  
Qi Jia ◽  
...  

ABSTRACT Background Parkinson's disease (PD) is a common neurodegenerative disorder. Cinnamon procyanidin oligomers (CPOs) are flavonoids with many claimed health benefits. Objective This study aimed to elucidate the neuroprotection of A-type CPOs (CPO-A) and the underlying mechanisms in cultured cell and animal models of PD. Methods Thirty male mice (C57BL/6, 9-wk old) were assigned to 3 groups (n = 10), and were given daily gavage of saline [control and 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) groups] or CPO-A (150 mg/kg, CPO-A group) during days 1–15 and daily intraperitoneal injections of saline (control group) or MPTP (20 mg/kg; MPTP and MPTP + CPO-A groups) during days 11–15. After the motor behavior test, all mice were killed on day 16 to collect the substantia nigra (SN) for assaying the neuroprotective effects of CPO-A. SH-SY5Y cells were treated with 12.5 μM CPO-A for 2 h or 3 activators of stress-related kinases (5–25 μM) for 12–48 h followed by 1 mM 1-methyl-4-phenylpyridinium (MPP+) for assays of viability, morphology, and stress status. Results Compared with the control, the MPTP treatment decreased (P < 0.05) locomotor activity by 21%, and tyrosine hydroxylase (TH) positive neurons by 55% and Th mRNA concentration by 51% in the SN. The CPO-A treatment attenuated or restored (P < 0.05) these changes and inhibited (P < 0.05) the MPTP-induced activation of P38 mitogen-activated protein kinase (P38MAPK) and P53, along with the downstream expression of BCL-2 associated X protein (BAX) in the SN. In SH-SY5Y cells, the CPO-A treatment blocked (P < 0.01) the MPP+-induced accumulation of intracellular reactive oxygen species and neurotoxicity. However, this protection was abolished (P < 0.05) by activators of the P38MAPK/P53/BAX pathway. Conclusion CPO-A protected against MPP+-induced cytotoxicity in SH-SY5Y cells and MPTP-induced neurotoxicity in mice by regulating the P38MAPK/P53/BAX signaling. Our findings reveal a novel role and mechanism of a food flavonoid CPO-A in preventing neurodegeneration.


2019 ◽  
Vol 97 (12) ◽  
pp. 1159-1168
Author(s):  
Fatma F. Ali ◽  
Walaa Yehia Abdelzaher ◽  
Randa Ahmed Ibrahim ◽  
Doaa Mohamed Elroby Ali

Although heme oxygenase-1 (HO-1) is part of an endogenous defense system implicated in the homeostatic response, its role in cell proliferation and tumor progression is still controversial. Endometrial hyperplasia (EH) is associated with high risk of endometrial cancer (EC). Therefore, we aimed to evaluate the effect of hemin, a HO-1 inducer, against EH. Thirty-two female rats (60–70 days old) were divided into 4 groups treated for 1 week: vehicle control group, hemin group (25 mg/kg; i.p. 3 times/week), estradiol valerate (EV) group (2 mg/kg per day, p.o.), and hemin plus EV group. Sera were obtained for reduced glutathione level. Uterine malondialdehyde, superoxide dismutase, total nitrite/nitrate, and interleukin-1β levels were estimated. HO-1 and p38 mitogen-activated protein kinase expressions were obtained in uterine tissue. Uterine histological and immunohistochemical assessment of iNOS and Ki67 were also done. Results demonstrated that upregulation of HO-1 expression in hemin plus EV rats led to amelioration of EH which was confirmed with histological examination. This was associated with significant decrease in oxidative stress parameters, p38 mitogen-activated protein kinase expression, and interleukin-1β level. Also, uterine iNOS and Ki67 expressions were markedly suppressed. In conclusion, upregulation of HO-1 expression via hemin has ameliorative effect against EH through its antioxidant, anti-inflammatory, and antiproliferative actions.


2014 ◽  
Vol 26 (1) ◽  
pp. 130
Author(s):  
N. Z. Saraiva ◽  
C. S. Oliveira ◽  
M. del Collado ◽  
M. R. de Lima ◽  
R. Vantini ◽  
...  

Chemical enucleation using microtubule-depolymerizing drugs is an attractive procedure to simplify the enucleation process in nuclear transfer. The aim of this study was to optimize chemically assisted (CA) and chemically induced (CI) enucleation protocols using metaphase II (MII) and pre-activated bovine oocytes, respectively, and to evaluate the activity of maturation promoting factor (MPF) and mitogen-activated protein kinase (MAPK) in cytoplasts generated by these techniques. Initially, we determined the shortest effective treatment of MII and activated oocytes with 0.05 μg mL–1 demecolcine. Bovine oocytes in vitro matured (IVM) for 19 h (MII) or activated artificially with 5 μM ionomycin (5 min) and 10 μg mL–1 cycloheximide (5 h) after 26 h IVM were treated with demecolcine and samples were collected at 0, 0.25, 0.5, 1.0, 1.5, and 2.0 h of treatment. Oocytes were then stained with 10 μg mL–1 Hoechst 33342 and the protrusion or enucleation rates were determined. Next, we evaluated histone H1 and myelin basic protein (MBP) kinases, reflecting MPF and MAPK activities, respectively, in oocytes obtained from these treatments, and for that we used the method described by Kubelka et al. (2000 Biol. Reprod. 62, 292–302). Protrusion and enucleation rates were evaluated by the chi-squared (χ2) test, and MPF and MAPK activities were submitted to ANOVA and Tukey's test at 5% significance. For MII oocytes, effects of demecolcine were observed as early as 15 min, with a significant difference (P < 0.05) between control (12/112, 10.7%) and treated (33/114, 28.9%) groups in relation to protrusion rates. The largest number of protrusions was observed after 1.0 h of treatment (control: 15/113, 13.3%a; treated: 45/111, 40.5%b). In pre-activated oocytes, effects of demecolcine were also observed after 15 min, and in both techniques there were no significant differences between groups treated with demecolcine for 1.0, 1.5, or 2.0 h (CA: 40.5 to 52.5% of protrusion; CI: 35.2 to 46.7% of enucleation). In contrast to previous reports in which high concentrations of demecolcine for CA enucleation increased MPF activity, we observed no alterations in the activity of this factor at a demecolcine concentration of 0.05 μg mL–1. Activity of MAPK also did not differ significantly between the control and treated groups throughout evaluation. In the CI technique, a significant difference in MPF activity was observed after 0.5 h (70.3%) and 2.0 h of activation (39.1%), considering that the activity was 100% at the beginning of the evaluation. However, we observed no significant difference between the control and treated groups at any of the time points studied, as verified for MAPK activity. The exact effect of MPF on the nucleus in mammals is not well established. We believe that the use of low concentrations of demecolcine for short periods is less damaging to embryonic development and, until we have a better understanding of the effect of these kinases on the transferred nucleus, we recommend its use for chemical enucleation protocols in bovine. Financial support: FAPESP 2010/20744-6 and 2011/12983-3.


2013 ◽  
Vol 91 (8) ◽  
pp. 625-632 ◽  
Author(s):  
Borbála Balatonyi ◽  
Balázs Gasz ◽  
Viktória Kovács ◽  
János Lantos ◽  
Gábor Jancsó ◽  
...  

The antioxidant glutathione-S-transferase (GST) is a crucial determinant of the development of ischaemic−reperfusion (I/R) injury, and plays a pivotal role in the regulation of the mitogen activated protein kinase (MAPK) pathways involved in stress response and apoptosis. The aim of this study was to investigate whether inhibition of GST can abolish the benefit of ischaemic postconditioning (IPoC). A neonatal rat cardiomyocyte cell culture was prepared and divided into 6 groups: (I) control group without treatment; (II) cells exposed to simulated I/R; (III) simulated I/R (sI/R) with IPoC; (IV) ethacrynic acid (EA) alone; (V) sI/R with EA; and (VI) sI/R and IPoC together with EA. Viability of the cells was measured by MTT assay, the quantity of apoptotic cells was assessed by flow cytometry following annexin V-FITC − propidium-iodide double staining. The activation of JNK, p38, ERK/p42-p44 MAPKs, and GSK-3β protein kinase was determined by flow-cytometric assay. GST inhibition markedly increased the apoptosis and decreased the cell viability despite IPoC. The protective effect of IPoC was lost in GST-inhibited groups for all MAPKs and GSK-3β. GST activity is required for the survival of cultured cardiomyocytes under stress conditions. GST inhibition was associated with differential activation of MAP and the protein kinases regulating these pathways in the process of ischaemic postconditioning.


2014 ◽  
Vol 26 (2) ◽  
pp. 245 ◽  
Author(s):  
Mohammad Bozlur Rahman ◽  
Leen Vandaele ◽  
Tom Rijsselaere ◽  
Mohamed Shehab El-Deen ◽  
Dominiek Maes ◽  
...  

Heat stress has long been recognised as a cause of subfertility in farm animals. The objectives of the present study were to elucidate the effect of heat stress on sperm function and involvement of the mitogen-activated protein kinase (MAPK) 14 signalling pathway. Spermatozoa incubated for 4 h at a physiological temperature (38.5°C) exhibited significantly (P < 0.05) reduced motility, plasma membrane integrity and mitochondrial potential compared with non-incubated spermatozoa; the reductions in these parameters were more severe following incubation at a hyperthermic (41°C) temperature (P < 0.01). Percentages of fertilisation and embryo development were highly affected in spermatozoa incubated at 41°C compared with non-incubated spermatozoa (P < 0.01). Similarly, embryo quality was adversely affected by sperm incubation at 41°C, as indicated by a higher apoptotic cell ratio in Day 7 blastocysts compared with that in the non-incubated control group (14.6% vs 6.7%, respectively; P < 0.01). Using SB203580 (10 µg mL–1), a specific inhibitor of the p38 MAPK pathway, during sperm hyperthermia reduced MAPK14 activation (24.9% vs 35.6%), increased sperm motility (45.8% vs 26.5%) and reduced DNA fragmentation (16.9% vs 23.4%) compared with the untreated control group, but did not improve subsequent fertilisation and embryo development. In conclusion, heat stress significantly affects the potential of spermatozoa to penetrate oocytes, as well as subsequent embryo development and quality. Notably, the data show that the MAPK14 signalling pathway is largely involved in heat-induced sperm damage. However, further research is needed to elucidate other signalling pathways possibly involved in heat-induced sperm damage.


2019 ◽  
Vol 7 (8) ◽  
pp. 1247-1251 ◽  
Author(s):  
Santi Syafril ◽  
Dharma Lindarto ◽  
Aznan Lelo ◽  
Rosita Juwita Sembiring ◽  
Awaluddin Saragih

BACKGROUND: Defects in post-receptor insulin signalling are the major cause of insulin resistance in type 2 diabetes mellitus (T2DM). AIM: This study aimed to investigate the correlations between insulin receptor substrate (IRS)-1 with phosphoinositide 3-kinase (PI3K) and p38 mitogen-activated protein kinase (MAPK) levels after puguntano (Curanga fel-terrae [Merr.]) leaf extract treatment in a rat model of T2DM. METHODS: A combination of high-fat diet-feeding (HFD) and multiple low dose intraperitoneal injections of streptozotocin was used to induced T2DM in 48 Wistar rats, which were then randomly divided into control and treatment groups (n = 24 per group). Puguntano leaf extract was administered to the treatment group once daily (200 mg/kg.bw) for 10 days. IRS-1, PI3K and p38 MAPK levels were measured in skeletal muscle using sandwich ELISAs in control group after becoming T2DM and in the treatment group after 10 days of puguntano treatment. Data were analysed using the Wilcoxon test and Spearman’s correlation. RESULTS: IRS-1, PI3K and p38 MAPK levels were significantly higher in the treatment group than in the control group. There were also significant positive correlations between IRS-1 with PI3K and p38 MAPK levels (r = 0.375, p = 0.035; r = 0.552, p = 0.003; respectively) after the treatment. CONCLUSION: This study demonstrated significant positive correlations between IRS-1 with PI3K and p38 MAPK levels after puguntano leaf extract treatment of T2DM rats.


2021 ◽  
Vol 11 (1) ◽  
pp. 51-58
Author(s):  
Baotong Shu ◽  
Yi Liu ◽  
Yu Ma ◽  
Li Li

To investigate parthenolide (PTL)’s effect to cisplatin (DDP) sensitivity in uveal melanoma and to show the underlying mechanism. Human uveal melanoma cell line M23 was split into the control group, PTL treatment group, DDP treatment group, PTL + DDP treatment group, DDP + Mitogen-activated protein kinase (MAPK) signal inhibitor (SB203580) treatment group, and PTL + DDP + MAPK signal activator (anisomycin) treatment group. CCK-8 test was conducted to detect cell viability, flow cytometry was utilized for cell apoptosis detection, and western blot was utilized to determine the phosphorylation of p38MAPK and JNK. Compared to the control group, PLT treatment group M23 cell activity, and expression of p-p38MAPK, p-JNK were reduced notably (P < 0.05). Meanwhile, these indices of DDP treatment group were lower than of the control group but higher than of the PTL treatment group. In the PTL + DDP treatment group M23 cell activity and expression level of p-p38MAPK, p-JNK was significantly lower than in the PTL and DDP treatment groups (P < 0.05). Inhibition of MAPK signal pathway increased the DDP effect to proliferation inhibition and apoptosis promotion. In contrast, MAPK signal pathway activator treatment alleviates PTL + DDP treatment effect on M23 cell line apoptosis and proliferation. Parthenolide (PTL) increased cisplatin (DDP) sensitivity in uveal melanoma through the inhibition of MAPK signal pathway.


2007 ◽  
Vol 19 (1) ◽  
pp. 265
Author(s):  
Y. X. Jin ◽  
X. S. Cui ◽  
W. K. Chang ◽  
T. Kim ◽  
N. H. Kim

Although evidence suggests that leptin modulates oocyte maturation in vitro, few studies have examined the direct effect of leptin on cytoplasmic maturation and pronuclear formation following fertilization of porcine oocytes.The aim of this studywas to determine microtubule and microfilament assembly following oocyte maturation, and to assess blastocyst formation, mitogen-activated protein kinase (MAPK) activity, and pronuclear formation following parthenogenetic stimuli or intracytoplasmic sperm injection (ICSI) of leptin-treated oocytes.A symmetrical shape of the meiotic spindle was considered to be the normal microtubule assembly, and a clear, thick microfilament area containing a second metaphase chromatin was considered to be morphologically normal. Significant differences were determined using Tukey's multiple range test with P &lt; 0.05 being considered significant. Addition of 10 ng mL-1 of leptin to the in vitro maturation (IVM) medium significantly increased the percentage of zygotes that developed to the blastocyst stage (26.1 � 2.1%; P &lt; 0.05) compared with that of the control (0 ng mL-1: 16.3 � 2.8%) or 1 ng mL-1 (18.6 � 2.6%) leptin treatment groups following parthenogenetic activation. After IVM for 44 h, the percentage of oocytes with normal microtubules was higher in the leptin (10 ng mL-1) group than in the control group (89.1 � 4.3% vs. 78.5 � 4.0%, respectively; P &lt; 0.05). However, the percentage of normal microfilament assembly was similar in the leptin-treated and control groups (85.6 � 4.3% and 82.9 � 5.0%, respectively). In oocytes matured in vitro in the presence of 10 ng mL-1 of leptin and subsequently induced by parthenogenetic activation via chemical stimulation, there was a significant increase in the formation of 2 pronuclei (2PN: 52.1 � 5.2%; P &lt; 0.05) at 6 h, compared with the control non-leptin-treated oocytes (40.7 � 4.0%). Similarly, addition of 10 ng mL-1 of leptin to the IVM medium also increased 2PN formation at the same time point following ICSI (leptin treatment: 47.9 � 4.0; control: 36.2 � 3.8%; P &lt; 0.05). The addition of 10 ng mL-1 of leptin to the IVM medium decreased the level of phospho-ERK1/2 at 6 and 9 h and was lower in the leptin-treated group compared with the control non-leptin-treated group (P &lt; 0.01). These results suggest that exogenous leptin enhances cytoplasmic maturation and pronuclear formation following fertilization, possibly via the MAPK pathway.


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