Inhibitory Effects of Some Antibiotics on Activity of Carbonic Anhydrase from Rainbow Trout Erythrocytes in Vitro and in Vivo

Gill Ca2+ transport (GCAT) in fish is regulated by a number of different hormones. Stanniocalcin (STC) from the corpuscles of Stannius (CS) is an inhibitor of GCAT, whereas pituitary-derived prolactin and cortisol stimulate GCAT. Other than this, however, little is known about the effects of other hormones on this important transport process. The role of calcitonin (CT) in calcium homeostasis in fish is still controversial. Whereas many studies have shown significant effects of CT on plasma calcium levels, an equal number of studies have failed to find any correlations between plasma calcium and CT levels in fish. Previous in vitro studies have shown that salmon CT has potent inhibitory effects on GCAT in isolated, perfused fish gill preparations, a finding that has never been corroborated in vivo. Therefore, in this report we examined the effects of salmon CT on whole body 45Ca uptake (as a measure of GCAT) in young rainbow trout. In support of the in vitro findings, we found that CT had significant inhibitory effects on GCAT. In parallel studies, we found that CT had no effects on STC secretion and only modest, stimulatory effects on STC mRNA levels in cultured trout CS cells. These finding suggest that both CT and STC function as negative regulators of GCAT in fish.

Download Full-text

Effect of vitamin E on carbonic anhydrase enzyme activity in rainbow trout (Oncorhynchus mykiss) erythrocytes in vitro and in vivo

Acta Veterinaria Hungarica ◽

10.1556/avet.52.2004.4.4 ◽

2004 ◽

Vol 52 (4) ◽

pp. 413-422 ◽

Cited By ~ 59

Author(s):

Ş. Aras-Hisar ◽

O. Hisar ◽

Ş. Beydemir ◽

I. Gülçin ◽

T. Yanik

Keyword(s):

Enzyme Activity ◽

Rainbow Trout ◽

Vitamin E ◽

Carbonic Anhydrase ◽

Oncorhynchus Mykiss ◽

Rainbow Trout Oncorhynchus Mykiss ◽

Blood Erythrocyte ◽

The Difference

Considering that the excessive usage of vitamin E causes hypervitaminosis and thus reduces blood erythrocyte concentrations, therefore it is worth studying how its pharmacological dosage affects the activity of carbonic anhydrase (CA) enzyme found in erythrocytes of rainbow trout (Oncorhynchus mykiss) in vitro and in vivo. Vitamin E inhibited CA enzyme and the IC50 value of the vitamin was 0.039 mM in vitro. Similarly, it was seen that vitamin E inhibited CA enzyme activity after the first hour following vitamin E injections in vivo. The activities of CA in groups of trout given vitamin E injection were measured at 1, 3 and 5 h and the corresponding activities were found to be 772.7 ± 290.5 (P < 0.05), 1286.4 ± 378.2 and 1005.7 ± 436.1 enzyme units (EU) g Hb-1. The difference over the control was significant (P < 0.05) in the first hour and insignificant at 3 and 5 h (P ? 0.05). The activity of CA in the control, which did not contain vitamin E, was determined as 1597.7 ± 429.0 EU g Hb-1.

Download Full-text

In vitro and in vivo effects of some pesticides on carbonic anhydrase enzyme from rainbow trout (Oncorhynchus mykiss) gills

Pesticide Biochemistry and Physiology ◽

10.1016/j.pestbp.2010.01.003 ◽

2010 ◽

Vol 97 (3) ◽

pp. 177-181 ◽

Cited By ~ 36

Author(s):

Saltuk Buğrahan Ceyhun ◽

Murat Şentürk ◽

Orhan Erdoğan ◽

Ömer İrfan Küfrevioğlu

Keyword(s):

Rainbow Trout ◽

Carbonic Anhydrase ◽

Oncorhynchus Mykiss ◽

Rainbow Trout Oncorhynchus Mykiss ◽

In Vivo Effects ◽

Carbonic Anhydrase Enzyme

Download Full-text

Combination of a novel growth hormone releasing hormone Antagonist JMR 132 and Tamoxifen enhances the inhibitory effects on growth of ZR 75 and T47D estrogen dependent human breast cancer cells in vitro and in vivo

Geburtshilfe und Frauenheilkunde ◽

10.1055/s-0029-1225201 ◽

2009 ◽

Vol 69 (05) ◽

Author(s):

S Buchholz ◽

AV Schally ◽

A Krishan ◽

A Papadia ◽

O Ortmann ◽

...

Keyword(s):

Breast Cancer ◽

Growth Hormone ◽

Human Breast Cancer ◽

Breast Cancer Cells ◽

Growth Hormone Releasing Hormone ◽

Human Breast Cancer Cells ◽

Human Breast ◽

Inhibitory Effects

Download Full-text

Inhibitory effects of epimedium herb water extract on the inflammatory response in vitro and in vivo

Planta Medica ◽

10.1055/s-0036-1596615 ◽

2016 ◽

Vol 81 (S 01) ◽

pp. S1-S381

Author(s):

YC Oh ◽

YH Jeong ◽

WK Cho ◽

SJ Lee ◽

JY Ma

Keyword(s):

Inflammatory Response ◽

Water Extract ◽

Inhibitory Effects

Download Full-text

The Effects of Brinolase (Fibrinolytic Enzyme from Aspergillus Oryzae) on Platelet Aggregation of Dog and Man

Thrombosis and Haemostasis ◽

10.1055/s-0038-1649039 ◽

1972 ◽

Vol 28 (01) ◽

pp. 031-048 ◽

Cited By ~ 4

Author(s):

W. H. E Roschlau ◽

R Gage

Keyword(s):

Platelet Aggregation ◽

Aspergillus Oryzae ◽

Degradation Products ◽

Blood Platelet ◽

Human Platelets ◽

Fibrinolytic Enzyme ◽

Inhibitory Effects ◽

Blood Platelet Aggregation

SummaryInhibition of blood platelet aggregation by brinolase (fibrinolytic enzyme from Aspergillus oryzae) has been demonstrated with human platelets in vitro and with dog platelets in vivo and in vitro, using both ADP and collagen as aggregating stimuli. It is suggested that the optimal inhibitory effects of brinolase occur indirectly through the generation of plasma fibrinogen degradation products, without compromising platelet viability, rather than by direct proteolysis of platelet structures.

Download Full-text

Inhibitory Effects of a Reengineered Anthrax Toxin on Canine Oral Mucosal Melanomas

Toxins ◽

10.3390/toxins12030157 ◽

2020 ◽

Vol 12 (3) ◽

pp. 157 ◽

Cited By ~ 2

Author(s):

Adriana Tomoko Nishiya ◽

Marcia Kazumi Nagamine ◽

Ivone Izabel Mackowiak da Fonseca ◽

Andrea Caringi Miraldo ◽

Nayra Villar Scattone ◽

...

Keyword(s):

Tumor Cells ◽

Evaluation Criteria ◽

Anthrax Toxin ◽

Treatment Modalities ◽

Inhibitory Effects ◽

Upa Receptor ◽

New Treatment ◽

Oral Malignancy

Canine oral mucosal melanomas (OMM) are the most common oral malignancy in dogs and few treatments are available. Thus, new treatment modalities are needed for this disease. Bacillus anthracis (anthrax) toxin has been reengineered to target tumor cells that express urokinase plasminogen activator (uPA) and metalloproteinases (MMP-2), and has shown antineoplastic effects both, in vitro and in vivo. This study aimed to evaluate the effects of a reengineered anthrax toxin on canine OMM. Five dogs bearing OMM without lung metastasis were included in the clinical study. Tumor tissue was analyzed by immunohistochemistry for expression of uPA, uPA receptor, MMP-2, MT1-MMP and TIMP-2. Animals received either three or six intratumoral injections of the reengineered anthrax toxin prior to surgical tumor excision. OMM samples from the five dogs were positive for all antibodies. After intratumoral treatment, all dogs showed stable disease according to the canine Response Evaluation Criteria in Solid Tumors (cRECIST), and tumors had decreased bleeding. Histopathology has shown necrosis of tumor cells and blood vessel walls after treatment. No significant systemic side effects were noted. In conclusion, the reengineered anthrax toxin exerted inhibitory effects when administered intratumorally, and systemic administration of this toxin is a promising therapy for canine OMM.

Download Full-text

Protective effects of carbonic anhydrase inhibition in brain ischaemia in vitro and in vivo models

Journal of Enzyme Inhibition and Medicinal Chemistry ◽

10.1080/14756366.2021.1907575 ◽

2021 ◽

Vol 36 (1) ◽

pp. 964-976

Author(s):

Ilaria Dettori ◽

Irene Fusco ◽

Irene Bulli ◽

Lisa Gaviano ◽

Elisabetta Coppi ◽

...

Keyword(s):

Carbonic Anhydrase ◽

Protective Effects ◽

Brain Ischaemia ◽

In Vivo Models ◽

Carbonic Anhydrase Inhibition

Download Full-text

Trichostatin A downregulates bromodomain and extra-terminal proteins to suppress osimertinib resistant non-small cell lung carcinoma

Cancer Cell International ◽

10.1186/s12935-021-01914-y ◽

2021 ◽

Vol 21 (1) ◽

Author(s):

Yuting Meng ◽

Xixi Qian ◽

Li Zhao ◽

Nan Li ◽

Shengjie Wu ◽

...

Keyword(s):

Trichostatin A ◽

Small Cell Lung Carcinoma ◽

Cell Types ◽

Inhibitory Effects ◽

Cell Lung Carcinoma ◽

Growth Inhibitory ◽

Terminal Proteins ◽

P Cells

Abstract Background The third-generation epithelial growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) have shown significant therapeutic effects on patients with non-small cell lung carcinoma (NSCLC) who carry active EGFR mutations, as well as those who have developed acquired resistance to the first-generation of EGFR-TKIs due to the T790M mutation. However, most patients develop drug resistance after 8–10 months of treatment. Currently, the mechanism has not been well clarified, and new therapeutic strategies are urgently needed. Methods Osimertinib resistant cell lines were established by culturing sensitive cells in chronically increasing doses of osimertinib. The anticancer effect of reagents was examined both in vitro and in vivo using the sulforhodamine B assay and a xenograft mouse model. The molecular signals were detected by western blotting. The combination effect was analyzed using CompuSyn software. Results We found that bromodomain and extra-terminal proteins (BETs) were upregulated in osimertinib resistant (H1975-OR) cells compared with those in the paired parental cells (H1975-P), and that knockdown of BETs significantly inhibited the growth of H1975-OR cells. The BET inhibitor JQ1 also exhibited stronger growth-inhibitory effects on H1975-OR cells and a greater expression of BETs and the downstream effector c-Myc than were observed in H1975-P cells. The histone deacetylase (HDAC) inhibitor trichostatin A (TSA) showed stronger growth suppression in H1975-OR cells than in H1975-P cells, but vorinostat, another HDAC inhibitor, showed equal inhibitory efficacy in both cell types. Consistently, downregulation of BET and c-Myc expression was greater with TSA than with vorinostat. TSA restrained the growth of H1975-OR and H1975-P xenograft tumors. The combination of TSA and JQ1 showed synergistic growth-inhibitory effects in parallel with decreased BET and c-Myc expression in both H1975-OR and H1975-P cells and in xenograft nude mouse models. BETs were not upregulated in osimertinib resistant HCC827 cells compared with parental cells, while TSA and vorinostat exhibited equal inhibitory effects on both cell types. Conclusion Upregulation of BETs contributed to the osimertinib resistance of H1975 cells. TSA downregulated BET expression and enhanced the growth inhibitory effect of JQ1 both in vitro and in vivo. Our findings provided new strategies for the treatment of osimertinib resistance.

Download Full-text