“…Although NO is less active in cells from normal mice ( 43 ), a spleen cell subpopulation produces enough NO during an in vitro immune response to completely prevent multiplication of T cells ( 44 , 45 ). Similarly, previous studies have demonstrated that a wide range of potential immunomodulatory functions may be expected for NO in the thymus, including the following: Induction of tolerance, restriction of major histocompatibility complex, lymphocyte trafficking and regulation of thymic endocrine output ( 33 , 36 , 37 , 42 ). Furthermore, if there are effects or changes in the cells due to BetA treatment, it is assumed that NO may be produced to perform its regulatory roles in the cells of these immune organs.…”