Nagai H, Takaoka Y, Mori H, Matsuura N
Department of Pharmacology, Gifu Pharmaceutical University, Japan.
Inflamm Res. 1996 Jun;45(6):293-8. doi: 10.1007/BF02280994.
The effects of mesoporphyrin, a novel porphyrin derivative, on type II collagen-induced arthritis in mice were studied. Mesoporphyrin (10-30 mg/kg) and prednisolone (5 mg/kg; reference drug) reduced the incidence and severity of type II collagen-induced arthritis in mice, as assayed by clinical observation and histopathological studies. Although both agents inhibited type II collagen-induced delayed type hypersensitivity in arthritic mice, only prednisolone inhibited humoral immunity to type II collagen. The effects of mesoporphyrin on T cell dependent allergic inflammation were examined, in order to study the mechanism by which it inhibits arthritis. Staphylococcal enterotoxin B (SEB; superantigen)-potentiated collagen-induced arthritis and sheep red blood cell-induced delayed type hypersensitivity reaction were clearly inhibited by mesoporphyrin. Moreover, the superantigen-induced CD-25 expression on T cells was inhibited by mesoporphyrin. These results indicate that mesoporphyrin inhibits type II collagen-induced arthritis by inhibiting the activation of T cells.
研究了新型卟啉衍生物中卟啉对小鼠Ⅱ型胶原诱导性关节炎的影响。通过临床观察和组织病理学研究测定,中卟啉(10 - 30mg/kg)和泼尼松龙(5mg/kg;参比药物)降低了小鼠Ⅱ型胶原诱导性关节炎的发病率和严重程度。虽然两种药物均抑制了关节炎小鼠中Ⅱ型胶原诱导的迟发型超敏反应,但只有泼尼松龙抑制了对Ⅱ型胶原的体液免疫。为了研究中卟啉抑制关节炎的机制,检测了其对T细胞依赖性变应性炎症的影响。中卟啉明显抑制了葡萄球菌肠毒素B(SEB;超抗原)增强的胶原诱导性关节炎和绵羊红细胞诱导的迟发型超敏反应。此外,中卟啉抑制了超抗原诱导的T细胞上CD - 25的表达。这些结果表明,中卟啉通过抑制T细胞的活化来抑制Ⅱ型胶原诱导性关节炎。