谷氨调节硫化的释放,以及Diallyl多硫化化合物的眼睛的低压作用
Susmit Mhatre1,2,3, Rai Anjali1,4,5, Pulkit Sahai1
1Department of Pharmacy Sciences, School of Pharmacy and Health Professionals, Creighton University, Omaha, NE 68178, USA.
Pharmaceuticals (Basel, Switzerland)
|October 26, 2024
概括
谷氨 (GSH) 增强了硫化 (H2S) 从二二硫化 (DADS) 和二三硫化 (DATS) 中的释放,从而降低了眼内压力 (IOP). 雌性子对这种降血压效应的敏感性较小.
科学领域:
- 眼科医生 眼科 眼科
- 神经科学是一个神经科学.
- 生物化学 生物化学
背景情况:
- 硫化 (H2S) 作为一种内源性神经递质.
- H2S 在调节水性幽默动态方面发挥作用.
- H2S为视网膜神经元提供神经保护.
研究的目的:
- 评估从二二硫化物 (DADS) 和二三硫化物 (DATS) 中释放的H2S.
- 在子中研究DADS和DATS对眼部低血压的影响.
- 检查谷氨 (GSH) 对H2S释放和眼部低血压作用的影响.
主要方法:
- 使用H2S-生物传感器量化H2S释放.
- 在子的眼内压力 (IOP) 通过气动度计的测量.
- 在雄性和雌性子中使用DADS和DATS,包括和没有GSH.
主要成果:
- 在体外,GSH显著增加了来自DADS和DATS的H2S释放.
- DADS和DATS在雄性和雌性子中都显示出IOP的剂量依赖性降低.
- 格拉斯增强了DADS和DATS的内血压降低作用.
结论:
- GSH增强了H2S释放和DADS和DATS的眼部低血压效应.
- 观察到的效应取决于多硫化物中硫原子的数量.
- 与雄性相比,雌性子对IOP降低效应的敏感性较低.
相关概念视频
Open Angle Glaucoma: Treatment
397
In open-angle glaucoma, the iridocorneal angle remains open, but the trabecular meshwork becomes stiff, slowing down the outflow of aqueous humor. This causes a buildup of aqueous humor in the anterior chamber, leading to a sudden increase in intraocular pressure. The treatment for open-angle glaucoma focuses on reducing the elevated intraocular pressure by either decreasing the secretion of aqueous humor or increasing its outflow.
Drugs such as carbonic anhydrase inhibitors, α2- and...
Drugs such as carbonic anhydrase inhibitors, α2- and...
397
Preparation and Reactions of Sulfides
4.7K
Sulfides are the sulfur analog of ethers, just as thiols are the sulfur analog of alcohol. Like ethers, sulfides also consist of two hydrocarbon groups bonded to the central sulfur atom. Depending upon the type of groups present, sulfides can be symmetrical or asymmetrical. Symmetrical sulfides can be prepared via an SN2 reaction between 2 equivalents of an alkyl halide and one equivalent of sodium sulfide.
4.7K
Preparation and Reactions of Thiols
6.0K
Thiols are prepared using the hydrosulfide anion as a nucleophile in a nucleophilic substitution reaction with alkyl halides. For instance, bromobutane reacts with sodium hydrosulfide to give butanethiol.
6.0K
Antihypertensive Drugs: Thiazide-Class Diuretics
548
Thiazide diuretics are sulfonamide derivatives featuring a benzothiadiazine ring system in their molecular structure. Based on this structure, thiazide diuretics can be categorized into two groups: thiazide-type and thiazide-like diuretics. Thiazide-type diuretics, including hydrochlorothiazide and chlorothiazide, consist of a benzothiadiazine backbone with an attached sulfonamide group. Thiazide-like diuretics, such as chlorthalidone and indapamide, lack the thiazide ring but demonstrate...
548
Cholinergic Antagonists: Pharmacokinetics
412
Cholinergic antagonists—such as antimuscarinics—are available in oral, topical, ocular, parenteral, and inhalational formulations. Most antimuscarinics are oral formulations, while scopolamine is available as a topical patch, and ipratropium and tiotropium are available as inhalation aerosols or powders. Atropine, tropicamide, and cyclopentolate are topically instilled in the eye. Most antimuscarinics are lipid-soluble and readily absorbed from the gastrointestinal tract and...
412
Structure and Nomenclature of Thiols and Sulfides
4.6K
Thiols and sulfides are sulfur analogs of alcohols and ethers, respectively, where the sulfur atom takes the place of the oxygen atom. Thus, thiols are generally represented as RSH, where R is an alkyl substituent and —SH is the functional group. On the other hand, in sulfides, the central sulfur atom is bonded to two hydrocarbon groups on either side. Depending upon the type of group, sulfides can be either symmetrical or asymmetrical. Both thiols and sulfides display a bent geometry,...
4.6K


