Idänpään-Heikkilä JJ - Search Results

1

mu- and delta-opioid receptor antisense oligodeoxynucleotides antagonize morphine-induced growth hormone secretion in rats.

Idänpään-Heikkilä JJ, Rauhala P, Männistö PT. Idänpään-Heikkilä JJ, et al. Eur J Pharmacol. 1995 Sep 15;284(1-2):227-30. doi: 10.1016/0014-2999(95)00462-t. Eur J Pharmacol. 1995. PMID: 8549632

2

N-nitro-L-arginine attenuates development of tolerance to antinociceptive but not to hormonal effects of morphine.

Rauhala P, Idänpään-Heikkilä JJ, Tuominen RK, Männistö PT. Rauhala P, et al. Eur J Pharmacol. 1994 Jun 23;259(1):57-64. doi: 10.1016/0014-2999(94)90157-0. Eur J Pharmacol. 1994. PMID: 7957594

3

Differential disappearance of tolerance to thermal, hormonal and locomotor effects of morphine in the male rat.

Rauhala P, Idänpään-Heikkilä JJ, Tuominen RK, Männistö PT. Rauhala P, et al. Eur J Pharmacol. 1995 Oct 4;285(1):69-77. doi: 10.1016/0014-2999(95)00392-x. Eur J Pharmacol. 1995. PMID: 8846813

4

Morphine withdrawal alters anterior pituitary hormone secretion, brain endopeptidase activity and brain monoamine metabolism in the rat.

Idänpään-Heikkilä JJ, Rauhala P, Tuominen RK, Tuomainen P, Zolotov N, Männistö PT. Idänpään-Heikkilä JJ, et al. Pharmacol Toxicol. 1996 Mar;78(3):129-35. doi: 10.1111/j.1600-0773.1996.tb00193.x. Pharmacol Toxicol. 1996. PMID: 8882344

5

Neuroendocrine effects of dexmedetomidine: evidence of cross-tolerance between a mu-opioid agonist and an alpha 2-adrenoceptor agonist in growth hormone secretion of the male rat.

Idänpään-Heikkilä JJ, Rauhala P, Männistö PT. Idänpään-Heikkilä JJ, et al. Pharmacol Toxicol. 1996 Mar;78(3):136-42. doi: 10.1111/j.1600-0773.1996.tb00194.x. Pharmacol Toxicol. 1996. PMID: 8882345

6

Cold exposure attenuates effects of secretagogues on serum prolactin and growth hormone levels in male rats.

Rauhala P, Idänpään-Heikkilä JJ, Lang A, Tuominen RK, Männistö PT. Rauhala P, et al. Am J Physiol. 1995 Apr;268(4 Pt 1):E758-65. doi: 10.1152/ajpendo.1995.268.4.E758. Am J Physiol. 1995. PMID: 7733277

7

In mononeuropathic rats, the enhancement of morphine antinociception by L-365,260, a selective CCK(B) receptor antagonist, depends on the dose of systemic morphine and stimulus characteristics.

Idänpään-Heikkilä JJ, Perrot S, Guilbaud G, Kayser V. Idänpään-Heikkilä JJ, et al. Eur J Pharmacol. 1997 May 1;325(2-3):155-64. doi: 10.1016/s0014-2999(97)00123-4. Eur J Pharmacol. 1997. PMID: 9163562

8

The antinociceptive activity of kappa- but not delta-opioid receptor agonists is maintained in morphine-tolerant neuropathic rats.

Catheline G, Kayser V, Idänpään-Heikkilä JJ, Guilbaud G. Catheline G, et al. Eur J Pharmacol. 1996 Dec 30;318(2-3):273-81. doi: 10.1016/s0014-2999(96)00790-x. Eur J Pharmacol. 1996. PMID: 9016915

9

Different roles of alpha 2-adrenoceptors of the medulla versus the spinal cord in modulation of mustard oil-induced central hyperalgesia in rats.

Mansikka H, Idänpään-Heikkilä JJ, Pertovaara A. Mansikka H, et al. Eur J Pharmacol. 1996 Feb 15;297(1-2):19-26. doi: 10.1016/0014-2999(95)00725-3. Eur J Pharmacol. 1996. PMID: 8851161

10

The effects of ethanol in combination with the alpha 2-adrenoceptor agonist dexmedetomidine and the alpha 2-adrenoceptor antagonist atipamezole on brain monoamine metabolites and motor performance of mice.

Idänpään-Heikkilä JJ, Björn M, Seppälä T. Idänpään-Heikkilä JJ, et al. Eur J Pharmacol. 1995 Jan 13;292(2):191-9. doi: 10.1016/0926-6917(95)90012-8. Eur J Pharmacol. 1995. PMID: 7536679

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