Hui-Fei Cui, Xue-Liang, ¹Department of Biochemical Pharmaceutics, Shandong Medical Univers ity, Jinan 250012, China
²Department of Gastroenterology, Chinese PLA General Hospital of Jinan Command, Jinan 250031, China
Hui-Fei Cui, female, born on 1968-01-09 in Shanghai, graduated from S handong Medical University in 1993 with a master degree, engaged in the research of drug preparation, having 20 papers published.
Supported by the National Fund for New Drug Research and Development, No.96-901-05-103 and the Commitee of Science and Technology, S handong Province, No.9575
Correspondence to: Hui-Fei Cui, Department of Biochemical Pharm aceutics, Shandong Medical University, Jinan 250012, China
Telephone: +86-531-2600132
Email.xiaohuak＠jn-public.sd.cninfo.net
Received: 1999-04-15 Revised: 1999-06-18

Subject headings: colitis; ulcerative/drug therapy; heparin/th erapertic use; corticosteroid-resistant

Cui HF, Jiang XL. Treatment of corticosteroid-resistant ulcerative colitis with oral low molecular weight heparin.
World J Gastroentero, 1999;5(5):448-450

INTRODUCTION
The etiology and pathogenesis of ulcerative colitis (UC) have remained unclear. Treatment is nonspecific based on the anti- inflammatory agents corticosteroid and sulfasalazine. A significant proportion fail to respond to this therapy^［1］. As the relapse, refractory or serious UC patients had a hypercoagulable state and an increased incidence of thromboembolic events^［2-4］, heparin has been used by some authors^［5-7］. Yet, its half-life period is short, needing long-term injection, which restricts its further clinical application. Our previous studies have demonstrated oral LMWH not only overcomes the shortcomin gs of common heparin^［8,9］, but also has anti-inflammatory effects^［10,11］. The aim of this paper is to study the therapeutic effects and mechani sm of oral LMWH in patients with corticosteroid-resistant UC.

MATERIALS AND METHODS
Clinical materials
There were eight men and twelve women aged 21 years to 56 years (mean 33 years). All cases were histologically confirmed and met the diagnostic standard of chronic non-infectious intestinal disease of China (Taiyuan meeting, 1993), including seventeen cases of severe, and three moderate UC. Duration of diseases ranged from 8 months to 11 years (mean 4.1 years). Rectal bleeding, diarrhea, mucus s tool, abdominal pain were the main symptoms. Four patients were associated with thromboembolic diseases. All patients were treated with high-dose corticosteroi d and sulfasalazine for more than 4 weeks without effect, sulfasalazine was mai tained in combination with oral LMWH (366U/kg, twice daily) for more than 4 weeks. Prednisolone was tapered and stopped.

Monitoring parameters
Assessment of platelet activation and aggregability^［2,4］. We used a sensitive flow cytometric technic designed to minimize sample handling and render fixation unnecessary to quantify platelet activation. Blood samples were incubated by 10 minutes of venesection with fluorescein isothiocyanate (FITC) conjugated antibodies to the platelet surface antigens, P-selectin (CD_62P) and CD₆₃ (Immunotech, Marseilles, France). Analysis was made within 15 minutes of venesection using a BD (Becton Dickinson Immonocytometry Systems) FAC Scan. TXA-2 (Suzhou Medical College) was measured using RIA method, samples wer e taken without tourniquet into chilled tubes containing 1∶9 anticoagulant/ antiaggregant solution (trisodium cirrate 3.8%), centrifuged for 15min-30min, later at 4℃ for 30 minutes to minimize in vitro activation, supernatant was decanted off and stored at -20℃ for assay within 3 months. Platelet aggregatio n rates (PAR) and thrombosis length (TL) in vitro were assessed by XSN-RⅡ instrument according to the manufecturer′s instruction.

Measurment of CD₅₄. CD₅₄ in blood and tissues were measured using flow cytometric technic according to our previous report^［12］.

Assessment of efficacy^［7］
Pre- and post-treatment scores were calculated for the following disease parameters: ① Stool frequency (average number per day for the past week). ② Rectal bleeding (0: absent, 1: streak of blood on stools occationally, 2: obvious blood on stool frequently, 3: complete bloody stools). ③ Colonoscopic appearance 0: normal vascular pattern, 1: mild lesion (loss of vascular pattern, mucosa edema, no ble eding), 2: moderate lesion (granularity and friability of the mucosa), 3: severe lesion (discrete ulceration and spontancous bleeding). ④ Histological grading: serial biopsies of the rectum and the colon were taken. Five histological chang es seen in UC (cellular infiltrate in the lamina propria, cryptitis, crypt absce ss formation, golet cell depletion, and regenerative hyperplasia of the epitheli um) each were scored from 0 (absent) to 3 (severe), a total UC score of 5 or les s indicated mild disease, a score of 5-10, moderate, and a score of 10-15 severe desease. ⑤ General health status (0: excellent, 1: good, 2: poor, 3: poorer, 4: very poor, 5: poorest).

Statistical analysis
Student′s t test and Friedman test were used to assess the significance of differences between mean pre- and post-treatment parameters.

RESULTS
Therapeutic effects
Nineteen patients (95.0%) achieved clinical remission (normal stool frequency and no rectal bleeding) on a combination of oral LMWH and sulfasalazine. One patient had reduced rectal bleeding only. The average period of marked improvement was 2.9 weeks (range 1 week-4 weeks), and of remission was 5 weeks (range 1 week-12 weeks). Rectal bleeding ceased in 19 patients (5 patients within 5 days -8 days, the others within 2 weeks-7 weeks). Nineteen patients had general heal th condition improved earlier on oral LMWH, than bowel symptoms. There were highly significant improvement in mean scores for all disease parameters (Table 1).

Table 1 Therapeutic effects of oral LMWH in corticosteroid-resist ant UC patients

^bP＜0.01 vs pretr eatment.

Blood contents of CD_62P, CD₆₃, TXA², platelet aggregation rate (PAR) and thrombosis length (TL) in vitro
All the indexes in corticosteroid-resistant UC patients increased significantly as compared with the normal controls (P＜0.01). After treatment with oral LMWH, all the parameters of UC patients decreased (P＜0.01), but CD_62P and CD₆₃ remained higher than normal (P＜0.01), (Table 2).

Table 2 Effects of oral LMWH on CD_62P and CD₆₃, TXA₂ , platelet aggregation rate (PAR) and thrombosis length (TL) in vitro in UC patients (mean±SD)

^aP＜0.05, ^bP＜0.01 vs normal person; ^dP＜0.01 vs pretreatment.

CD₅₄ in blood and tissues
CD₅₄ elevated in both blood and tissues in corticosteroid-resistant UC patients (P＜0.01), CD₅₄ in tissues being higher than in blood. Afteroral LMWH, CD₅₄ lowered significantly in both blood and tissues (P＜0.01), but still higher than that of normal controls (P＜0.05), (Table 3).

Table 3 Effects of oral LMWH on CD₅₄ in UC patients (mean±SD,%)

^aP＜0.05, ^bP＜0.01 vs normal; ^dP ＜0.01 vs post-treatment.

Complications
No serious complications were associated with the use of oral LMWH.

DISCUSSION
Heparin, a group of sulphated glycosaminoglycans, in addition to its physiological effects and anticoagulant, antithromboembolic, antiallergic, antiviral, antiendotoxic and immunoregulative biological activities, has a wide range of potenti ally anti-inflammatory effects, including inhibition of neutrophil elastase and inactivation of chemokines^［5,13］.Compared with heparin, LMWH has a enhanced antithromboembolic effects, longer half life period, less bleeding tendency, higher bioavailability, easier absorption by oral administration^［8,9］, and has the anti inflammatory effects as well^［10,11］. Previous reports^［5-7］on improvement in UC patients treated with heparin prompted us to perform a pilot study of oral LMWH to find a more convenient and effective drug for patients with corticosteroid-resistant UC. The observed response to oral LMWH is paradoxical. Nineteen of 20 patients with corticosteroid-resistant UC achie ved clinical remission and became asymptomatic on oral LMWH combined with sulfas alazine. Opposite to the traditional idea that heparin can enhance bleeding, rec tal bleeding was the first symptom to be improved by oral LMWH. The results are similar to other reports of heparin treatment^［5-7］.
      If oral LMWH has a therapeutic effect in UC, its mechanism of action should shed some light on the elusive pathogenesis of this disease. There are several thrombophilic features of UC that suggest the effect of oral LMWH on colitic symptoms may be attributable to its anticoagulant and antithrombotic properties. Evidence of a thrombotic process in UC includes: reports of a hypercoagulable state^［2-4］, an increased incidence of thromboembolic event^［14］, and ischemic complications such as toxic megacolon and pyoderma gangrenosum. In this stud y, the membrane marks of platelet activity CD_62P and CD₆₃ increased significantly, and the derivative of active platelet TXA-2 also elevated, sugge sting that the blood platelet was in an active state, which not only led to a hy percoagulable state and an increased incidence of thromboembolic events, but als o enhanced inflammatory reaction^［24］.Activated hyperaggregable platelets in the mesenteric circulation could amplify the inflammatory cascade by promoting neutrophil recruitment and chemotaxis. P-selectin has an established action as the adhesion molecule for neutrophils, and circulating platelet aggregates may contribute to ischemic damage and infarction by occluding the intestinal microvasculature. Platelet derived thromboxane A₂ may also contribute to the ischemia by inducing local vasocontriction. After treatment with oral LMWH, all these par ameters dropped markedly, suggesting that the therapeutic effect of LMWH is part ly related to inhibition of platelet activity^［9］. CD₅₄ antigen rea cts with the 85kD-110kD integral membrane glycoprotein, is also known as an intercellular adhesion molecule-1 (ICAM-1) expressed on endothelial cells and both resting (weak) and activated (moderate) lymphocytes and monocytes. CD₅₄ is l igand for the leukocyte function antigen-1 (CD_11a. Its expression is up- regulated upon stimulation by inflammatory mediators such as cytokines and LPS, and it is involved in B cell-T cell co-stimulatory interations. In this study, CD₅₄ elevated significantly in blood and tissues of UC patients, being in tissues higher than in blood_［12］. Therefore, it could reflect the infla mmation of intestinal mucosa. After oral LMWH, CD₅₄ dropped significantly in both blood and tissues, indicating that oral LMWH could relieve the inflammat ory activity in these patients who received prednisolone for a long period (more than 4 weeks) and had no significant improvement and were regarded as corticost eroid-resistant refractory cases of UC. In other reports^［5］, heparin ca n also inhibit c-reactive protein (CRP), tumor necrosis factor (TNF) and L-se lectin of UC patients. The detailed mechanisms by which the anti-inflammatory properties of oral L MWH are mediated in UC remain to be elucidated further.
      From these results, we conclude that oral LMWH may play a role in treating corticosteroid resistant UC, the mechanism is partly related to inhibition of platelet activity, hypercoagulable state and anti-inflammatory effects. No serious complications were found associated with the use of oral LMWH.

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