2021
DOI: 10.1016/j.ejmech.2021.113517
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Hybrids between H2S-donors and betamethasone 17-valerate or triamcinolone acetonide inhibit mast cell degranulation and promote hyperpolarization of bronchial smooth muscle cells

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Cited by 15 publications
(14 citation statements)
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“…Important inhibitory effects on mast cell degranulation have been observed, due to a reduction in the release of β-hexosaminidase which was more effective compared to the corresponding native drugs. Compounds 92 and 93 established an important membrane hyperpolarization of BSMCs and have been shown to be more effective than the reference compound NS1619 [ 258 ].…”
Section: H 2 S Donors and Diseasesmentioning
confidence: 99%
“…Important inhibitory effects on mast cell degranulation have been observed, due to a reduction in the release of β-hexosaminidase which was more effective compared to the corresponding native drugs. Compounds 92 and 93 established an important membrane hyperpolarization of BSMCs and have been shown to be more effective than the reference compound NS1619 [ 258 ].…”
Section: H 2 S Donors and Diseasesmentioning
confidence: 99%
“…On this ground, H 2 S‐releasing agents (also named H 2 S donors) seem to be adequate for either mimicking the endogenous H 2 S generation under physiological conditions, or replenishing additional H 2 S for both diagnostic and therapeutical purposes. During the past years, substantial endeavor has been made to develop various H 2 S donors, and a number of H 2 S donors with different releasing rates and mechanisms have been reported 101,105–125 . H 2 S donors, regarded as the exogenous suppliers of H 2 S, could be employed as the ideal candidates for the treatment of diseases whose H 2 S‐associated networks might be short‐circuited.…”
Section: Introductionmentioning
confidence: 99%
“…These steroids possess anti-inflammatory, antiseptic, antishock effects with minimal prominent adverse effects. [90] Guo et al used HA to construct a rapidly dissolving microneedles patch to enhance the transdermal delivery of BSP-BDP for the treatment of oral ulcers. [91] As shown in Figure 5a, BSP-BDP@MNs exhibited sufficient mechanical strength to penetrate the mucous membrane of the rat tongue abdomen with an insertion depth of about 207 ± 3 μm through a straightforward preparation process.…”
Section: Oral Ulcermentioning
confidence: 99%
“…These steroids possess anti‐inflammatory, antiseptic, antishock effects with minimal prominent adverse effects. [ 90 ] Guo et al. used HA to construct a rapidly dissolving microneedles patch to enhance the transdermal delivery of BSP‐BDP for the treatment of oral ulcers.…”
Section: Microneedles For Oral Disease Treatmentmentioning
confidence: 99%