Keller Camryn L, Jones Nicholas T, Abadie Raegan B, Barham William, Behara Raju, Patil Shilpadevi, Paladini Antonella, Ahmadzadeh Shahab, Shekoohi Sahar, Varrassi Giustino, Kaye Alan D
School of Medicine, Louisiana State University Health Sciences Center, Shreveport, USA.
Department of Anesthesiology, Louisiana State University Health Sciences Center, Shreveport, USA.
Cureus. 2024 Jan 8;16(1):e51894. doi: 10.7759/cureus.51894. eCollection 2024 Jan.
Peptic ulcers are a common condition that arises from an imbalance between acid production and gastroduodenal protective factors. Various drugs, including non-steroidal anti-inflammatory drugs (NSAIDs), potassium supplements, bisphosphonates, and doxycycline, can increase the development of peptic ulcers. NSAIDs are one of the most common medications prescribed for pain relief, and they also inhibit the formation of cyclooxygenase-1 (COX-1). COX-1 helps in the production of mucus that lines the stomach, so by inhibiting COX-1, NSAIDs reduce the mucus produced by the stomach and increase the likelihood of gastric ulcer formation. Additionally, NSAIDs are acidic, and increasing the amount of any acid in the stomach can result in promoting ulcer development. Potassium supplements are used to reduce the effects of hypertension, decrease the development of kidney stones, and treat hypokalemia. The various types of transporters and channels used to move potassium across cell membranes increase hydrogen being pumped, increasing gastric acid production and ulcer formation. Bisphosphonates are used to treat a variety of skeletal disorders that require inhibition of osteoclast activity. Nitric oxide (NO) has been shown to have a therapeutic effect on gastric ulcers, and some bisphosphonates have been shown to decrease the production of nitric oxide, resulting in increased damage to the gastric mucosa. Finally, doxycycline is a broad-spectrum tetracycline antibiotic that is typically used to treat anthrax poisoning, skin lesions, and sexually transmitted diseases. A harmful adverse effect of doxycycline is the formation of peptic and gastric ulcers related to the drug being highly acidic once it has dissolved.
消化性溃疡是一种常见疾病,由胃酸分泌与胃十二指肠保护因子之间的失衡引起。包括非甾体抗炎药(NSAIDs)、钾补充剂、双膦酸盐和强力霉素在内的多种药物会增加消化性溃疡的发生风险。NSAIDs是最常用于缓解疼痛的药物之一,它们还会抑制环氧化酶-1(COX-1)的形成。COX-1有助于胃内黏液的产生,因此通过抑制COX-1,NSAIDs会减少胃产生的黏液,增加胃溃疡形成的可能性。此外,NSAIDs呈酸性,胃内任何酸性物质的增加都可能导致溃疡发展。钾补充剂用于减轻高血压的影响、减少肾结石的发生以及治疗低钾血症。用于使钾跨细胞膜转运的各种转运体和通道会增加氢离子的泵出,从而增加胃酸分泌和溃疡形成。双膦酸盐用于治疗各种需要抑制破骨细胞活性的骨骼疾病。一氧化氮(NO)已被证明对胃溃疡有治疗作用,一些双膦酸盐已被证明会减少一氧化氮的产生,从而导致胃黏膜损伤增加。最后,强力霉素是一种广谱四环素类抗生素,通常用于治疗炭疽中毒、皮肤损伤和性传播疾病。强力霉素的一个有害副作用是形成与药物溶解后高度酸性相关的消化性溃疡和胃溃疡。