Kynurenine and Neopterin Levels in Patients with Rheumatoid Arthritis and Osteoporosis During Drug Treatment

犬尿氨酸 类风湿性关节炎 新喋呤 巴比妥酸 吲哚胺2,3-双加氧酶 医学 内科学 黄脲酸 犬尿氨酸途径 邻氨基苯甲酸 内分泌学 药理学 色氨酸 药品 受体 化学 谷氨酸受体 生物化学 氨基酸
作者
Caroline M. Forrest,Alan Kennedy,Trevor W. Stone,Nicholas Stoy,L. Gail Darlington
出处
期刊:Advances in Experimental Medicine and Biology [Springer Nature]
卷期号:527 (52417): 287-295 被引量:59
标识
DOI:10.1007/978-1-4615-0135-0_32
摘要

The kynurenine pathway from tryptophan generates compounds which can act on glutamate receptors in peripheral tissues or modulate free radical activity. We have measured the concentrations of several of these compounds in the plasma of patients with rheumatoid arthritis (RA) and osteoporosis (OP) before treatment with drugs and then at monthly intervals for 6 months during treatment. Kynurenine analysis was performed by HPLC. Compared with healthy controls, RA patients showed significantly decreased baseline levels of tryptophan, 3-hydroxykynurenine and 3-hydroxyanthranilic acid and increased levels of kynurenine and xanthurenic acid, while kynurenic acid concentrations were normal. Different results were recorded from patients with OP with only a significant reduction in tryptophan and 3-hydroxyanthranilic acid when compared with healthy controls. During 6 months of treating the RA patients with prednisolone or methotrexate, and the OP patients with raloxifene or etidronate and calcium there were significant therapeutic responses and a significant trend towards a reduction in levels of neopterin in RA patients receiving methotrexate but no changes in the profiles of tryptophan metabolites. The results are consistent with the induction of indoleamine-2,3-dioxygenase (IDO) in both RA and OP but with far greater activation of the pathway in the much more inflammatory condition, i.e. RA. It is concluded that there are changes in the kynurenine pathway, which may modify the activation of tissue glutamate receptors, in RA and OP, but that these are not affected by the drug treatments studied.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
欧克欧克发布了新的文献求助10
刚刚
刚刚
AAA完成签到,获得积分10
刚刚
中岛悠斗发布了新的文献求助10
刚刚
1秒前
浅风发布了新的文献求助10
1秒前
彭于晏应助123采纳,获得10
1秒前
Orange应助ATP采纳,获得10
2秒前
2秒前
2秒前
赘婿应助生动凝旋采纳,获得10
2秒前
3秒前
WZQ发布了新的文献求助10
3秒前
酷波er应助betsydouglas14采纳,获得10
4秒前
受伤青易完成签到,获得积分10
4秒前
4秒前
5秒前
5秒前
刘长绪完成签到,获得积分10
5秒前
pluto应助大方的小猫咪采纳,获得10
5秒前
hh应助搞怪代荷采纳,获得10
6秒前
wangyan完成签到,获得积分10
6秒前
6秒前
丘比特应助牧万万采纳,获得10
6秒前
6秒前
derrickZ完成签到 ,获得积分10
7秒前
隐形曼青应助闪闪机器猫采纳,获得10
7秒前
8秒前
8秒前
科研通AI6.1应助KKK采纳,获得30
8秒前
刘长绪发布了新的文献求助10
8秒前
竹子关注了科研通微信公众号
8秒前
吴宣京完成签到,获得积分10
9秒前
wangyan发布了新的文献求助10
9秒前
9527发布了新的文献求助10
9秒前
aloopp发布了新的文献求助10
9秒前
10秒前
李健应助坦率的刺猬采纳,获得10
10秒前
feng完成签到,获得积分20
10秒前
李雨发布了新的文献求助10
10秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Modern Epidemiology, Fourth Edition 5000
Kinesiophobia : a new view of chronic pain behavior 5000
Molecular Biology of Cancer: Mechanisms, Targets, and Therapeutics 3000
Propeller Design 1000
Weaponeering, Fourth Edition – Two Volume SET 1000
First commercial application of ELCRES™ HTV150A film in Nichicon capacitors for AC-DC inverters: SABIC at PCIM Europe 1000
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 内科学 生物化学 物理 计算机科学 纳米技术 遗传学 基因 复合材料 化学工程 物理化学 病理 催化作用 免疫学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 6003287
求助须知:如何正确求助?哪些是违规求助? 7512106
关于积分的说明 16107020
捐赠科研通 5148216
什么是DOI,文献DOI怎么找? 2758932
邀请新用户注册赠送积分活动 1735253
关于科研通互助平台的介绍 1631446