Abstract. The corpus luteum (CL) of the estrous cycle in the cow is a dynamic organ which has a lifespan of approximately 17-18 days. The main function of the CL is to produce progesterone (P) that requires for achievement and maintenance of pregnancy. If pregnancy does not occur successfully, the CL must regress within a few days to induce the next chance of ovulation. As the CL matures, the steroidogenic cells establish contact with many capillary vessels, consequently the CL is composed of a large number of vascular endothelial cells that can account for up to 50% of all cells. Therefore, blood vessels and blood flow within the CL have an essential role in luteal function. Nitric oxide (NO), a strong vasorelaxant, is now known to play key roles in a variety of physiological process. Indeed, NO has established itself as a polyvalent molecule which plays a decisive role in regulating multiple functions within female reproductive system. In the CL, NO is produced and regulates luteal blood flow, P secretion and apoptosis of luteal cells as well as endothelial cells. This review describes the current investigation for possible roles of NO in the luteolytic cascade within the bovine CL. Key words: Corpus luteum, Luteal blood flow, Luteolysis, Nitric oxide (J. Reprod. Dev. 56: [9][10][11][12][13][14] 2010) he corpus luteum (CL) is a transient organ in the ovary of mammals. The bovine CL rapidly develops within 2-3 days after ovulation, which is accompanied by an active angiogenesis and vascularization from the preovulatory follicle. The main function of the CL is to produce progesterone (P) that requires for achievement and maintenance of pregnancy [1]. If pregnancy does not occur successfully, the CL is only functional for 17-18 days and it must regress within a few days to induce the next chance of ovulation. In ruminants, it is well known that a pulsatile release of prostaglandin F2α (PGF2α) from the uterus on days 17-18 of the estrous cycle is essential to induce regression of the CL [2]. Luteolytic PGF2α induces a drastic decrease in P release from the CL as well as CL volume and blood flow to the CL in the non-pregnant cow [3,4]. Thus, it is easily considered that the bovine CL has well designed mechanisms by which development and regression are effectively controlled.In the cow, the CL is composed of a large number of vascular endothelial cells that can account for up to 50% of all the CL cells [5]. On the other hand, steroidogenic large luteal cells and small luteal cells constitute about 30% of all CL cells [5,6]. The bovine CL also has various cell types such as smooth muscle cells, pericytes, fibrocytes and immune cells, indicating that the CL is a heterogeneous tissue [7,8]. In addition, the CL is constituted by the condensed blood vasculature including large blood vessels and microcapillaries, and the majority of steroidogenic cells are adjacent to one or more capillaries [9]. It is known that a cell-to-cell interaction and these adhesions are essentially important for the CL integrity and physiolog...