Lubiprostone improves intestinal permeability in humans, a novel therapy for the leaky gut: A prospective randomized pilot study in healthy volunteers

被引:40
作者
Kato, Takayuki [1 ]
Honda, Yasushi [1 ]
Kurita, Yusuke [1 ]
Iwasaki, Akito [1 ]
Sato, Takamitsu [1 ]
Kessoku, Takaomi [1 ]
Uchiyama, Shiori [1 ]
Ogawa, Yuji [1 ]
Ohkubo, Hidenori [1 ]
Higurashi, Takuma [1 ]
Yamanaka, Takeharu [2 ]
Usuda, Haruki [3 ]
Wada, Koichiro [3 ]
Nakajima, Atsushi [1 ]
机构
[1] Yokohama City Univ, Dept Gastroenterol & Hepatol, Sch Med, Yokohama, Kanagawa, Japan
[2] Yokohama City Univ, Dept Biostat, Sch Med, Yokohama, Kanagawa, Japan
[3] Shimane Univ, Dept Pharmacol, Sch Med, Izumo, Shimane, Japan
关键词
TIGHT JUNCTION BARRIER; CROHNS-DISEASE; INFLAMMATION; CONSTIPATION; EXPRESSION; ENDOTOXIN; RESTORES; ARTICLE; BLOOD; ASSAY;
D O I
10.1371/journal.pone.0175626
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background and aims The barrier function of the small intestinal mucosa prevents the introduction of undesired pathogens into the body. Breakdown of this barrier function increases intestinal permeability. This has been proposed to induce not only gastrointestinal diseases, including inflammatory bowel disease and irritable bowel syndrome, but also various other diseases, including allergies, diabetes mellitus, liver diseases, and collagen diseases, which are associated with this so called "leaky gut syndrome As such, a method to prevent leaky gut syndrome would have substantial clinical value. However, no drugs have been demonstrated to improve disturbed intestinal permeability in humans to date. Therefore, we investigated whether a drug used to treat chronic constipation, lubiprostone, was effective for this purpose. Methods Healthy male volunteers were treated with lubiprostone (24 mu g/day) for 28 days. Intestinal permeability was evaluated by measuring the lactulose-mannitol ratio (LMR) after administration of diclofenac and compared with an untreated group. The examination was conducted three times in total, i.e., at baseline before diclofenac administration and after 14 and 28 days of lubiprostone treatment. Blood endotoxin activity was also evaluated at the same time points. Results The final analysis was conducted on 28 subjects (14 in the lubiprostone group and 14 in the untreated group). The LMR after 28 days of treatment was significantly lower in the lubiprostone group than that in the untreated group (0.017 vs. 0.028, respectively; 95% confidence interval, -0.022--0.0001; p = 0.049). Blood endotoxin activity exhibited almost no change over time in the lubiprostone and untreated groups and displayed no significant differences at any time point of examination. Conclusions This study is the first to report an improvement in leaky gut using an available drug in humans. The result suggests that lubiprostone may prevent and ameliorate "leaky gut syndrome". However, a pivotal trial is needed to confirm our finding.
引用
收藏
页数:13
相关论文
共 31 条
[1]   Alterations in intestinal permeability [J].
Arrieta, M. C. ;
Bistritz, L. ;
Meddings, J. B. .
GUT, 2006, 55 (10) :1512-1520
[2]   Combination of Lactobacillus helveticus R0052 and Bifidobacterium longum R0175 reduces post-myocardial infarction depression symptoms and restores intestinal permeability in a rat model [J].
Arseneault-Breard, Jessica ;
Rondeau, Isabelle ;
Gilbert, Kim ;
Girard, Stephanie-Anne ;
Tompkins, Thomas A. ;
Godbout, Roger ;
Rousseau, Guy .
BRITISH JOURNAL OF NUTRITION, 2012, 107 (12) :1793-1799
[3]   Activation of prostaglandin EP receptors by lubiprostone in rat and human stomach and colon [J].
Bassil, A. K. ;
Borman, R. A. ;
Jarvie, E. M. ;
McArthur-Wilson, R. J. ;
Thangiah, R. ;
Sung, E. Z. H. ;
Lee, K. ;
Sanger, G. J. .
BRITISH JOURNAL OF PHARMACOLOGY, 2008, 154 (01) :126-135
[4]   Intestinal epithelial responses to enteric pathogens: effects on the tight junction barrier, ion transport, and inflammation [J].
Berkes, J ;
Viswanathan, VK ;
Savkovic, SD ;
Hecht, G .
GUT, 2003, 52 (03) :439-451
[5]   EFFECT OF NONSTEROIDAL ANTIINFLAMMATORY DRUGS AND PROSTAGLANDINS ON THE PERMEABILITY OF THE HUMAN SMALL-INTESTINE [J].
BJARNASON, I ;
WILLIAMS, P ;
SMETHURST, P ;
PETERS, TJ ;
LEVI, AJ .
GUT, 1986, 27 (11) :1292-1297
[6]  
Davies NM, 1998, ALIMENT PHARM THER, V12, P303
[7]   Assessment of the Capability of a Gelling Complex Made of Tara Gum and the Exopolysaccharides Produced by the Microorganism Streptococcus thermophilus ST10 to Prospectively Restore the Gut Physiological Barrier A Pilot Study [J].
Del Piano, Mario ;
Balzarini, Marco ;
Carmagnola, Stefania ;
Pagliarulo, Michela ;
Tari, Roberto ;
Nicola, Stefania ;
Deidda, Francesca ;
Pane, Marco .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 2014, 48 :S56-S61
[8]   Lactobacillus casei prevents impaired barrier function in intestinal epithelial cells [J].
Eun, Chang Soo ;
Kim, Yong Seok ;
Han, Dong Soo ;
Choi, Joo Hyun ;
Lee, A. Reum ;
Park, Yoon Kyung .
APMIS, 2011, 119 (01) :49-56
[9]   Intestinal barrier: An interface between health and disease [J].
Farhadi, A ;
Banan, A ;
Fields, J ;
Keshavarzian, A .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2003, 18 (05) :479-497
[10]   Intestinal permeability in Behcet's syndrome [J].
Fresko, I ;
Hamuryudan, V ;
Demir, M ;
Hizli, N ;
Sayman, H ;
Melikoglu, M ;
Tunç, R ;
Yurdakul, S ;
Yazici, H .
ANNALS OF THE RHEUMATIC DISEASES, 2001, 60 (01) :65-66