Jack Rose, Ph.D.
- Professor of Physiology
- Assistant Chair for Graduate Programs
- (208) 282-4261
- Gale Life Sciences Bldg, Rm 306/307
- Reproductive Endocrinology Laboratory
- Reproduction, blastocyst implantation, uterus, uterine physiology, glycogen, mink, rats
- Ph.D. Animal Science (Reproductive Endocrinology) 1985 Oregon State University, Corvallis
- M.S. Zoology 1979 The Ohio State University, Columbus
- B.S. Natural Resources 1975 The Ohio State University, Columbus
- Assoc. Mechanical Engineering Technology, 1971 The University of Cincinnati, Cincinnati, Ohio
During my doctoral program at Oregon State University I had the opportunity to conduct research in two quite different areas of endocrine physiology. Those being, (1): the hormonal regulation of blastocyst implantation in the mink, a species exhibiting delayed implantation, and (2): the role of hormones in regulating the onset of winter fur growth in the mink.
In the area of reproduction, that work culminated in the demonstration of prolactin receptors in the uterus of this species, which at the time was a novel concept. Today, others have shown that the mammalian uterus expresses genes for both prolactin and the prolactin receptor, strongly suggesting not only endocrine but autocrine and/or paracrine effects of prolactin on the uterus.
Much work needs to be done to determine which genes are regulated in the uterus by prolactin and their role in reproductive function. From the fur growth studies, a major contribution was the finding that the pineal hormone melatonin plays a critical role in controlling hair growth in this species, in part, through its inhibitory effects on prolactin secretion.
As a professor at Idaho State University, research efforts during my early years were focused principally upon the effects of adrenal hormones in regulating hair growth cycles. We demonstrated that bilateral adrenalectomy of mink, induced almost immediate onset of hair growth cycles, that interestingly, appeared to cycle continuously with only brief, if any, resting (telogen) periods. Thus, instead of only two hair growth cycles each year, such animals might cycle as many as 6 times, or more. Injections of the adenohypophysial hormone ACTH (adrenocorticotropin) into the skin of mink induced local onset of hair growth cycles. This finding contributed to a rapidly growing field of research, wherein others have demonstrated that the skin of mammals expresses most if not all, of the hormones and their receptors that constitute the "stress-response" system. That is, corticotropin releasing hormone (CRH), CRH receptors, ACTH, and ACTH receptors.
Currently, I have returned to the study of reproductive endocrinology. Specifically, we are investigating the potential role of catecholestrogens in preparing the uterus for blastocyst implantation. Major catecholestrogens, are 2- and 4-hydroxylated molecules of the parent estrogen, estradiol. It is known that the uterus converts estradiol, produced by the ovaries, to such catecholestrogens, which then exert biological actions on both the uterus and blastocyst. The local production of CE's by the uterus, and their actions on that organ, are novel concepts. Catecholestrogens are metabolized very rapidly, such that little if any makes its way into the systemic circulation. Thus, their actions are of a paracine and/or autocrine in nature, having profound, and we believe, very important physiological effects, which can not be detected through the measurement of blood concentrations of the hormone metabolites.
We are presently, examining the effects of the catecholestrogens, 2-hydroxycatecholestradiol (2-OHE2) and 4-hydroxycatecholestradiol (4-OHE2) on glycogen metabolism in the uteri of rats and mink. Our most recent efforts show that 4-OHE2 stimulates glycogen accumulation in the rat uterus, equal to that of estradiol. Moreover, 4-OHE2 had a much greater effect on the uterine glandular epithelial cells of the rat, than on the luminal epithelium. And, finally, the effects of 4-OHE2 were significantly greater in parous rats (those that have previously given birth) when compared to nulliparous animals (those that have not yet produced offspring). This latter finding may, in part, explain why litter sizes in rats are almost always greater after the first pregnancy.
Many exciting studies await to be conducted in this most fascinating field of reproduction research. Ultimately, we hope that our efforts will contribute to a better understanding of blastocyst implantation. Because a high percentage of reproductive failures take place after fertilization but prior to implantation, we envision that the efforts of this type of research may one day contribute to a pharmacological means of improving blastocyst implantation. Such an outcome might lead to cures for some types of human infertility, increase farm animal production and perhaps be used to improve reproductive success in endangered species.
- BIOL 449 Human Physiology I, 4 credits
- BIOL 456 Human Physiology II, 4 credits
- BIOL 443 Endocrinology, 3 credits
- BIOL 301 Anatomy and Physiology, 4 credits, SUMMER
- BIOL 302 Anatomy and Physiology, 4 credits, SUMMER
Kabbaj, O., S.R. Yoon, C. Holm, J. Rose, M.L. Vitale and R.M. Pelletier. 2003. Relationship of the hormone sensitive lipase-mediated modulation of cholesterol metabolism in individual compartments of the testis to serum pituitary hormone and testosterone concentrations in a seasonal breeder, the mink (Mustela vison). Biol. Reprod., 68:722-734.
Johnston B, & J. Rose 1999 Prolactin and adrenal hormone interactions during the winter fur growth cycle in mink (Mustela vison). J. Exp. Zool., 284:437-444.
Rose, J., M. Kennedy, B. Johnston & W. Foster. 1998 Serum prolactin and dehydroepiandrosterone (DHEA) concentrations during the summer and winter hair growth cycles of mink (Mustela vison). Comp. Biochem. Physiol., Part A:121:263-271.
Rose, J. 1998 ACTH but not ?-MSH stimulates onset of hair growth in mink. J. Invest. Dermatol., 110:456-457.
Rose, J., OV Slayden and F. Stormshak. 1996. Melatonin-induced down regulation of uterine prolactin receptors in mink (Mustela vison). Gen. Comp. Endo. 103 101-106
Rose, J. 1995. Bilateral adrenalectomy induces early onset of summer fur growth in mink. (Mustela vison). Comp. Biochem. Physiol. 111C:243-247.
Rose, J., T. Garwood and B. Jaber. 1995. Prolactin binding site concentrations in the skin of mink during the winter fur growth cycle. J. Exp. Zool. 271: 205-210.
Garwood, T. and J. Rose. 1995. The effects of bilateral adrenalectomy on the initiation of fur growth cycles in the deer mouse. Lab. Anim. Sci.45: 564-566.
Rose, J., J-L Huang and R.A. Mead. 1993. The role of ovarian steroid hormones in the development of uterine prolactin receptors in the ferret. Biol. Reprod. 48:1266-1273.
Rose, J. and Wert, C. 1993. Prolactin binding sites in the adrenal glands of mink (Mustela vison). Comp. Biochem. Physiol. Vol. 104B:759-763.
Rose, J. and M. Sterner. 1992. The role of the adrenal glands in regulating the onset of winter fur growth in the mink. J. Exp. Zool. 262:469-473.
Rose, J., J. Oldfield and F. Stormshak. 1987. Apparent role of prolactin and melatonin in initiating winter fur growth in mink. Gen. Comp. Endocrinology 65:212-214.
Rose, J., J. Oldfield and F. Stormshak. 1986. Changes in serum prolactin concentrations and ovarian prolactin receptors during embryonic diapause in the mink. Biol. Reprod. 34:101-106.
Rose, J., F. Stormshak, J. Oldfield and J. Adair. 1985. The effects of photoperiod and melatonin on serum prolactin levels of mink during the autumn molt. J. Pineal Res. 2:13-19.
Rose, J., F. Stormshak, J. Oldfield and J. Adair. 1984. Induction of winter fur growth in mink (Mustela vison) with melatonin. J. Anim. Sci. 58:57-61.