ABSTRACT
In the current study, on the basis of 1,3,5-tris(2-methylimidazol-1-yl)benzene (timb), a designed tripodal connector, two new transition metal coordination polymers (CPs), {[Cu4(timb)2(Br-IPA)4]·5H2O}n (1) and {[Zn(timb)0.5(NH2-IPA)]·4H2O}n (2) have been generated with the mixed ligand method by the reaction between the timb and corresponding metal salts in the existence of dissimilar functional isophthalic acid (H2IPA) ligands. Furthermore, the Zn(II)-based complex 2 displays high sensitivity in the detection of Cu(II) ion in water. The neural stem cells proliferation after treated via compounds was detected with Cell Counting Kit-8 detection assay. And the real time reverse transcription polymerase chain reaction was carried out for the investigation of the differentiation function of the neural stem cells after the compound 1 treatment and compound 2 treatment. Further, molecular docking simulations confirmed that the biological activity that has been observed from experiments were from the carboxyl group on the Cu complex, in contrast, the imidazole groups were only used for binding with the Cu metal ion to retain the complex structure.
Subject(s)
Polymers , Imidazoles , Ligands , Molecular Docking SimulationABSTRACT
INTRODUCTION: A significant number of sensorineural hearing loss (SSNHL) patients had no noticeable hearing improvement after glucocorticoid (GC) treatment. In the present study, we examined expression of the nuclear factor erythroid 2-related factor 2 (NRF2) and histone deacetylase 2 (HDAC2) in peripheral blood mononuclear cells (PBMCs) of refractory SSNHL patients to study the role of NRF2-HDAC2 pathway in GC insensitivity hearing improvement after GC treatment, which is usually referred to as refractory SSNHL or GC insensitivity. MATERIALS AND METHODS: Forty-four refractory SSNHL patients were treated by intratympanic GC infusion. Hearing was tested in all patients before and after treatment by pure tone hearing test. NRF2/HDAC2 mRNA and protein levels were examined in PBMCs of refractory SSNHL patients before and after treatment. PBMCs from healthy volunteers were used as normal controls. RESULTS: According to the hearing improvement after treatment, patients were assigned into 2 groups: the intratympanic GC sensitive (IGCS) group (hearing recovery ≥15 dB HL) and the intratympanic GC insensitive (IGCI) group (hearing recovery <15 dB HL). Before treatment, the NRF2 mRNA level was lower in all patients than the normal control group. After treatment, NRF2 and HDAC2 mRNA and protein levels were increased in the IGCS group, while no significant change was observed in the IGCI group. CONCLUSION: Low response of NRF2/HDAC2 proteins is associated with GC insensitivity in SSNHL. We speculate that the NRF2-HDAC2 pathway affects GC sensitivity in SSNHL patients.
Subject(s)
Hearing Loss, Sensorineural , Hearing Loss, Sudden , Audiometry, Pure-Tone , Glucocorticoids/therapeutic use , Hearing Loss, Sensorineural/drug therapy , Histone Deacetylase 2/genetics , Humans , Leukocytes, Mononuclear , NF-E2-Related Factor 2/genetics , Treatment OutcomeABSTRACT
Glucocorticoids have been used to treat hearing loss and vestibular dysfunction for many years. However, some reports have indicated that a subset of patients with these disorders exhibit glucocorticoid insensitivity or resistance. A reduction in histone deacetylase 2 (HDAC2) activity and expression has been reported to play a critical role in glucocorticoid resistance. Here, we investigated the protective effects of aminophylline on HDAC2 expression and glucocorticoid sensitivity in lipopolysaccharide (LPS)-induced sudden sensorineural hearing loss in guinea pigs. We assessed hearing recovery in LPS-applied guinea pigs, which were either left untreated or were systemically treated with either dexamethasone, aminophylline, or a combination of the two. We utilized fluorescence microscopy and enzyme-linked immunosorbent assay to analyze the distribution patterns of HDAC2 and detect its levels in the cochlea. We used hematoxylin-eosin staining to examine cochlear histopathological changes. In the absence of treatment, significant hearing loss was detected in LPS-exposed animals. A synergistic effect was observed between aminophylline and dexamethasone in maintaining HDAC2 expression levels, preventing hearing loss in LPS-exposed animals and reducing cochlear damage. This study indicates that aminophylline can restore glucocorticoid sensitivity, which provides a new approach to treating patients with hearing disorders who are refractory to glucocorticoids.
Subject(s)
Aminophylline/pharmacology , Glucocorticoids/pharmacology , Hearing Loss, Sensorineural/etiology , Hearing Loss, Sensorineural/metabolism , Lipopolysaccharides/adverse effects , Animals , Cochlea/metabolism , Cochlea/physiopathology , Drug Synergism , Fluorescent Antibody Technique , Guinea Pigs , Hearing Loss, Sensorineural/diagnosis , Hearing Loss, Sensorineural/drug therapy , Histone Deacetylase 2/metabolism , Protective Agents/pharmacologyABSTRACT
OBJECTIVE: To study the cochlear function of patients with obstructive sleep apnea-hypopnea syndrome (OSAHS). METHODS: Transiently evoked otoacoustic emissions (TEOAEs) and Distortion-product otoacoustic emissions(DPOAEs) of 28 patients with OSAHS were measured one week before uvulopalatopharyngoplasty (UPPP) and six months after UPPP. RESULTS: In these patients the prevalence of TEOAEs was 64.3%, its spectral energy was mainly distributed between 0.5-2 kHz, the amplitudes of DPOAEs between 0.5-8 kHz were reduced significantly, the prevalences of DPOAEs at 0.5-8 kHz were between 46.4%-89.3%. After UPPP, the prevalences of TEOAEs and DPOAEs were increased, the amplitudes of DPOAEs were in turn (22.50 +/- 16.70) dB SPL, (5.83 +/- 2.69) dB SPL, (0.69 +/- 3.83) dB SPL, (-2.50 +/- 2.45) dB SPL, (4.95 +/- 2.65) dB SPL, (4.48 +/- 3.07) dB SPL from 0.5 kHz to 8 kHz, the amplitudes of DPOAEs were significantly increased at 1 kHz, 2 kHz, 4 kHz, 6 kHz, 8 kHz. CONCLUSION: OSAHS can affect the cochlear function of the patients with OSAHS, UPPP can improve the cochlear function.